U.S. PATENT AND TRADEMARK OFFICE
Information Products Division |
2000 ARCHIVE COPY
U.S. Patent Classification System - Classification Definitions
as of June 30, 2000
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For classification search strategies, please refer to the
Classification Index
Explanation of Data web page.
(definitions have been obtained from the
Patents ASSIST CD-ROM which
is produced by the U.S. Patent and Trademark Office
Electronic Products Branch)
Class 514
DRUG, BIO-AFFECTING AND BODY TREATING COMPOSITIONS
Class Definition:
Class 514 is an integral part of Class 424. It incorporates
all the definitions and rules as to subject matter of Class
424.
LINES WITH OTHER CLASSES AND WITHIN THIS CLASS
A. GENERAL STATEMENT OF CLASS SUBJECT MATTER
(1) Official subclasses 1-789 do not provide for
cross-reference patents which are originally classified in
Class 260 (Compound area) or in the Class 530-570 series or
in Class 585. Cross-reference patents that are originally
classified in the Class 520 series are allowed.
(2) The cross-reference rule elaborated above means that a
specific compound having a disclosed or even specifically
claimed utility (i.e., compound X useful as an anti-cancer
drug) will be classifiable only in Class 260 or in the Class
530-570 series or in class 585.
B. OFFICIAL CROSS-REFERENCE ART COLLECTIONS:
(1) Peptide and protein art collections (subclasses
800-809).
(2) Specifically disclosed disease condition and
pharmaceutical effect (subclasses 810-935).
The official cross-reference art collections subclasses
800-935 take patents dating from Jan.1, 1965. These
collections provide for data from all classes including
Classes 260, 530-570, and Class 585.
C. OFFICIAL CROSS-REFERENCE ART COLLECTIONS:
Subclasses 936-975 provide for specifically disclosed carrier
specified nonbioactive ingredient (subclasses 936-975).
This art collection provides (1) data from Class 260
(Compounds ) and Classes 530-570 series and Class 585 dating
from Jan. 1, 1965, and (2) data from all other classes
regardless of date.
Class 514 and Class 424 differ in scope as to
cross-referencing procedure. Those subclasses identified as
Class 424 will accept cross-references from all classes
including 424, 260, Classes 530-570 series and Class 585 as
has been done in the past. An exception within Class 424 are
subclasses 1.11+ wherein the 514 rule is respected and
therefore cross-referencing is not accepted.
SCHEDULE OUTLINE OF CLASS 514
The schedule is divided into a number of parts, each of which
is distinct and provides for different types of subject
matter. The following is a breakdown of the major areas and
indicates the type of subject matter provided therein.
(A) Subclasses 1-768 provide for the subject matter proper
under Class 424 containing a designated organic active
ingredient (DOAI), methods of making such compositions and
methods of using such compositions. Also included herein are
method of using a specified DOAI.
(B) Subclasses 769-771 provide for subject matter relating to
a designated inorganic nonactive ingredient (See Glossary
below) other than water or designated elemental nonactive
material (See Glossary). These subclasses provide for
compositions which may have an organic active material and
which active material does not qualify as a DOAI as well as
to methods of preparing or using such compositions. These
subclasses also provide for compositions containing a
designated inorganic nonactive material other than water or
designated elemental material and which composition qualifies
as subject matter proper for Class 424 and is not provided
higher in the classification schedule as well as to methods
of preparing or using such compositions.
(C) Subclasses 772-788 provide for subject matter relating to
a designated organic nonactive ingredient (See GLOSSARY)
other than a hydrocarbon. These subclasses provide for
compositions which may have an organic active material and
which active material does not qualify as a DOAI as well as
to methods of preparing or using such compositions.
(D) Subclass 789 is the miscellaneous subclass for subject
matter proper in Class 424 or 514. This subclass provides
for compositions, methods of preparing or using same.
(E) Subclasses 800-809 are art collections pertaining to
protein and peptide and relate to subject matter only in
Class 514.
(F) Subclasses 810-935 are art collections pertaining to
specifically disclosed disease condition and pharmaceutical
effect and relate to subject matter only in Class 514.
(G) Subclasses 936-975 are art collections pertaining to
specifically disclosed carrier system; physical form or
specified nonbioactive ingredient and relate to subject
matter only in Class 514.
DESIGNATED ORGANIC ACTIVE INGREDIENT (DOAI)
DOAI is when (a) the active ingredient is identified by at
least one chemical atom, e.g., organic phosphorus compound,
etc. or (b) the active ingredient is identified as a generic
type of chemical compound, e.g., alcohol, ether, etc.
The term active denotes a physiological, pharmacological or
biological effect.
For purposes of this class organic active ingredient although
inherently reciting the presence of a carbon atom is
considered to be too broad and therefore will not be
considered as DOAI's is as follows: chalcogen, carboxylic
acid, phosphorus containing, organic alkali or earth metal
compound, hydrocarbon, halogenated hydrocarbon, etc.
The following list below is not exhaustive and merely
emumerates certain materials that will not be considered as
DOAI's, e.g., organic compound, solvent, biocide,
pharmaceutically active, medicine, preservative, diabetes
active, pesticidal, active against rabies, antihistamine,
anti-tussive, anti-caries, crystalline, antioxidant, etc.
It is important to remember that function of a material or
even amount, e.g., pharmaceutical, etc., even if specific,
e.g., diabetes active, etc., or 2% of a diabetes active
ingredient, etc., does not meet any of the necessary criteria
elaborated in 1 and 2 above. Function or amount therefore
does not qualify as rendering an ingredient as "Designated".
RULES CONCERNING THE USE OF DOAI IN THE SCHEDULE
For purposes of Class 514, certain rules as to patent
placement have been adopted. These rules pertain only to the
subject matter in Class 514 and are not to be extrapolated to
areas in Class 424.
The rules adopted pertaining to the use of the term "DOAI"
are as follows:
(A) In those subclasses which recite a designated organic
active ingredient (DOAI) in the title, the indented
subclasses merely pertain to a further elaboration of the
DOAI and do not relate to any other ingredient. An example
of this is (subclass 497 in Class 514) which recites nitrogen
containing and is indented under (subclass 496) which recites
mercury and which in turn is indented under (subclass 492)
heavy metal containing DOAI. The meaning of (subclass 497)
is that an active ingredient contains both nitrogen and
mercury atoms as part of a single molecule.
(B) In those subclasses which recite "with" as in (subclass
168) under a specified DOAI, such use is consistent with the
term as used in other classes in that, at least two separate
materials must be present, one of which is the DOAI and the
other "with" ingredient. The "with" ingredient need not have
an active function for Class 514 unless the subclass
specifically requires an "active with ingredient" as in
subclass 154.
EXAMPLES OF PATENT PLACEMENT WITHIN THE CLASS
Patentee Claims
(A) A biocide and starch as a carrier. The original
classification is with the starch in subclass 778, since a
chemical atom of the biocide is not recited.
(B) 2% of a biocide and starch as a carrier. Same
classification as in (A) above, since 2% is not considered
sufficient to be DOAI.
(C) An organic phosphorus containing biocide and starch as
carrier. Original classification is on the basis of the
biocide since an atom is recited. Entirely proper to look at
disclosure to see the type of phosphorus compound encompassed
by the term "organic phosphorus".
(D) A synergistic mixture of two biocides at least one of
which is formaldehyde classifiable in subclasses 694+. The
disclosure recites that the other biocide can be a organic
phosphorus compound classifiable in subclasses 75+. Since
the claim has only one DOAI recited (i.e., formaldehyde)
original classification is in the formaldehyde species.
(E) A synergistic mixture of two biocides one of which is
formaldehyde and the other is malathion. Formaldehyde is
classified in subclass 694 and malathion is classified in
subclass 122. The original is classified with malathion in
subclass 122 as per normal classification rules.
RULES CONCERNING PLACEMENT OF SALTS WITHIN CLASS 514 AND
SEARCH THEREFOR
Classification Practice
(A) Inorganic salts of organic materials are considered as
organic and classified with the organic materials only, even
when the organic material is not a DOAI by definition (see
Glossary). No weight in the classification system is given
to the inorganic material. However, when the inorganic
segment of the salt is specifically claimed or disclosed as
the only active segment of the salt molecule original
classification is proper on the basis of the inorganic
segment and cross-referenced to the organic material.
Example 1. R--R. SO[subscrpt]4[end subscrpt]
classified on the basis of
R--R
segment only
Example 2 Organic. SO[subscrpt]4 [end subscrpt]
or
Organic pesticide. SO[subscrpt]4[end subscrpt] classified on
the basis of the disclosed organic or organic pesticide
material only.
Example 3. Organic. SO[subscrpt]4 [end subscrpt]
or
Amine. SO[subscrpt]4[end subscrpt]
Wherein activity is recited only in the SO[subscrpt]4[end
subscrpt] segment, original classification is with
SO[subscrpt]4[end subscrpt] segment, cross-reference is
highly desirable with the disclosed organic or amine
material.
(B) When a nonsalt DOAI material (see section 2, Glossary) as
well as a salt thereof are claimed a prima facie nonrebuttal
presumption is established that only the nonsalt active
material is effective, even if the salt is specifically
claimed and even if different 424 utility is noted for the
specific salt. The claims are classified as original with
the nonsalt DOAI material and a cross-reference to the salt
area, even if higher in the classification schedule is
unnecessary.
(C) When an organic salt of a DOAI is solely specifically
claimed (i.e., nonsalt species of material is not claimed)
the following classification rules will apply:
(1) Both segments of the solely claimed salt, i.e., anion and
cation, are designated
(a) both segments are claimed or disclosed as active for the
utility intended, or where no evidence is shown that a
particular segment is active or inactive (both through claims
or disclosure), the entire molecule will be considered a DOAI
and classified on the basis of the first appearing segment in
the schedule hierarchy, an example of this is the treatment
of amine-critic acid: original classification with citric
acid is proper since both segments of the molecule are active
and since amine is classified lower in the 514 schedule
hierarchy then citric acid or
(b) only one particular segment is claimed or disclosed as
active, the original classification is to the designated
active segment and cross-referenced to the nonactive segment
area if said nonactive segment is higher in the
classification schedule.
(2) Only one segment of the solely claimed salt, i.e., anion
or cation, is designated, the original classification is with
the active segment, even if the active segment is
nondesignated, e.g., "an amine salt of an organic compound"
wherein the pesticide or organic compound is specifically
claimed or disclosed to be active for the utility intended.
Classification is on the basis of the disclosed pesticide or
the organic compound and cross-referenced to the amine area
if the amine is higher in the schedule hierarchy than the
disclosed species of the pesticide or organic compound.
However, when the nondesignated segment is claimed as "a
pharmaceutically acceptable acid (or base or equivalent
thereof), e.g., "an amine salt of a therapeutically
acceptable or compatible acid", no weight is given to the
"acceptable or compatible acid" and classification is based
only on the designated segment, i.e., the amine.
Examination Practice
Due to the nature of the system of classification elaborated
above a search to be complete must at times entail searching
in a multiplicity of subclasses.
(A) Claims drawn to solely a salt. Claims are classified and
searched as in Classification Practice, C, above.
(B) Claims drawn to a nonsalt DOAI and also to a salt
thereof, either in a dependant claim or in a Markush group.
Classified only with the nonsalt species but searched in all
salt species which are classified higher in the
classification schedule than the nonsalt species.
The rules for determining Class placement of the Original
Reference (OR) for claimed chemical compositions are set
forth in the Class Definition of Class 252 in the section
LINES WITH OTHER CLASSES AND WITHIN THIS CLASS, subsection
COMPOSITION CLASS SUPERIORITY, which includes a hierarchical
ORDER OF SUPERIORITY FOR COMPOSITION CLASSES.
CLASS 514 TERMS
The following frequently used terms in Class 514 are
referenced in References to The Current Class, below. These
terms have also been entered into the Index of the U.S.
Patent Classification.
A
Acronycines; Allantion; Amantadine; Amphetamine; Ampicillin;
Amprotropine; Aspirin; Atropine
B
Barbituric acid; Benzocaine; Benzomorphans; Biotin
C
Capsaicin; Cephalocporins; Chlorpheniramine; Cholecalciferol;
Chrysanthemic acid; Cobalamin; Codeine; Colchicine;
Cortisone; Cupreine; Cycloheximide; Cyproheptadine; Cysteine
ester
D
DDT; DDVP; Dextromethorphan; Dyphylline
E
Ephedrine; Estradiol;
F
Fluspirilene
G
Glaucine; Glucamine; Griseofulvin
H
Hexachlorophene; Hydrocortisone
I
Isoniazid
M
Malathion; Melatonin; Meperidine; Methadone; Methapyrilene;
Methomyl; Morphinans; Morphine;
N
Nandrolone; Niacinamide; Nortestosterone; Novocaine
O
Oxolinic acid
P
Parathion; Pencillin G; Perimidines; Phenylephrine;
Phenyltoloxamine; Pilocarpine; Pimozide; Piromidic acid;
Perdnisolone; Procaine; Progesterone; Psoralen; Pteridine;
Purines
Q
Quinicine; Quinidine; Quinine; Quinoxaline
R
Riboflavins
S
Salinomycin; Scopolamine
T
Tartaric acid; Tetracycline; Theophilline; Thiamines;
Tocopherois; Tryptophan; Tyrosine; Tripelennamine
U
Uracil
V
Vinblastine; Vincamine; Viquidil
SEE OR SEARCH THIS CLASS, SUBCLASS:
52 Cobalamin
122 Malathion
132 Parathion
136 DDVP
152 Tetracycline
167 Cholecalciferol
165 Aspirin
178 Nortestosterone
179 Hydrocortisone
179 Cortisone
178 Nandrolone
179 Perdnisolone
177 Progesterone
182 Estradiol
198 Ampicillin
199 Pencillin G
200 Cephalocporins
249 Pteridine
249 Quinoxaline
251 Riboflavins
261 Purines
263 Theophilline
263 Dyphylline
269 Perimidines
270 Barbituric acid
274 Uracil
276 Thiamines
278 Fluspirilene
282 Codeine
283 Vincamine
283 Vinblastine
285 Acronycines
282 Morphine
284 Glaucine
289 Dextromethorphan
289 Morphinans
291 Oxolinic acid
291 Scopolamine
295 Benzomorphans
303 Piromidic acid
305 Cupreine
305 Quinidine
305 Quinine
314 Quinicine
314 Viquidil
323 Pimozide
325 Cyproheptadine
328 Cycloheximide
330 Meperidine
336 Methapyrilene
352 Tripelennamine
354 Isoniazid
355 Niacinamide
357 Chlorpheniramine
387 Biotin
390 Allantion
397 Pilocarpine
415 Melatonin
419 Tryptophan
455 Psoralen
458 Tocopherois
460 Salinomycin
462 Griseofulvin
477 Methomyl
534 Amprotropine
534 Atropine
535 Benzocaine
535 Novocaine
535 Procaine
550 Cysteine ester
567 Tyrosine
572 Chrysanthemic acid
574 Tartaric acid
627 Capsaicin
629 Colchicine
648 Methadone
651 Phenyltoloxamine
653 Ephedrine
653 Phenylephrine
654 Amphetamine
656 Amantadine
669 Glucamine
735 Hexachlorophene
748 DDT
GLOSSARY:
The following terms have been used in a number of subclass
titles throughout Class 514. For convenience, these often
used terms have been arranged into a Glossary. When any of
these terms is used in particular subclass titles in Class
514, their meaning is to be consistent with the meaning in
this Glossary.
ACYCLIC
Denotes a compound devoid of any ring-containing moiety.
Thus an acyclic chain may contain any atom as long as it is
not a member of a ring.
ALCOHOL
Denotes an organic compound having the general structure C-OH
wherein the carbon atom bound to the oxygen atom of the
hydroxyl group cannot be doubled bonded to oxygen, sulfur,
selenium, or tellurium or triple bonded to nitrogen. The
terms as used herein includes phenols.
ALDEHYDE
Denotes an organic compound having the general structure
-C-{C(=O)}[subscrpt]n [end subscrpt]-H or
H-{C(=O)}[subscrpt]n-[end subscrpt]H (n is 1 or more and
wherein the carbon atom bonded to the-{C(=O)}-[subscrpt]n[end
subscrpt] group is not double bonded to oxygen, sulfur,
selenium, or tellurium, or triple bonded to nitrogen.
ALICYCLIC RING OR RING SYSTEM
This term denotes a carbocyclic ring which is not a benzene
ring or a polycyclo carbocyclic ring system which does not
have a benzene ring as one of the cyclos.
AMINE-
Denotes an organic compound having a nitrogen atom single or
double bonded to a carbon atom and wherein the carbon atom
bonded to the nitrogen atom is devoid of a double bond to
oxygen, sulfur, selenium, or tellurium or triple bonded to
nitrogen. In addition, those compounds wherein the same
nitrogen atom is bonded to a -C(=X)- group (X is O, S, Se, or
Te) and to a carbon atom which is not double bonded to
oxygen, sulfur, selenium, or tellurium, are not considered as
being amines, e.g.,
-C-NH-C(X=)-
Although amides may be considered chemically as amines, it
has been found expedient for this class to exclude compounds
containing only amide nitrogen herefrom. Therefore, as used
throughout this area, the term amide is not to be confused as
being an amine. A compound, however, which contains a
nitrogen atom bonded to a non -C(=X)- carbon atom and which
contains either a nitrogen atom bonded to a -C(=X)- group or
an amide group, is considered as being an amine.
AMINO NITROGEN
Denotes any nitrogen in an organic compound other than a
nitrogen in an inorganic ion of an addition salt, a nitro
(-NO[subscrpt]2[end subscrpt]) or nitroso (-NO). Component
parts of an "adduct" will be considered to be attached to
each other ionically except if it is clear that the mode of
attachment is nonionic.
ARYL RING OR RING SYSTEM
This term denotes a benzene ring or a polycyclo carbocyclic
ring system having a benzene ring as one of the cyclos.
ATTACHED DIRECTLY OR BONDED DIRECTLY
These terms are used to show that specified moieties are
connected by bonds only.
ATTACHED INDIRECTLY
This term denotes that at least one atom, as well as bond,
connects specified moieties.
BENZENE RING
This term includes in all cases except where there are
explicit limitations to the contrary, substituted benzene
rings, including substitution in the form of an additional
fused or bridged ring or ring system.
BICYCLO RING SYSTEM
This term denotes a polycyclo ring system which contains
exactly two rings.
CARBOCYCLIC
This term denotes a ring or ring system where all ring
members are carbons.
CHAIN
This term denotes a plurality of atoms which connect
specified groups or atoms. The atoms of the chain must be
nonionically attached to each other and to the specified
groups or atoms. If the chain may not include any ring
members it will be designated as acyclic. When the chain may
include ring members the title will state that the chain may
include a ring. The chain ends where it attaches to the
specified groups or atoms and does not include any part of
them. The chain may have substituents but the substituents
are not part of the chain.
DESIGNATED ELEMENTAL NONACTIVE INGREDIENT
Denotes an elemental material either metallic or nonmetallic
and which is identified by its chemical nature, e.g., iron,
silver, etc., or is identified in a generic manner, e.g.,
alkali metal atom, etc. The term nonactive as used herein
denotes the absence of any physiological, pharmacological or
biological affect attributed to the elemental material.
DESIGNATED INORGANIC NONACTIVE INGREDIENT
Denotes an inorganic compound which is identified by at least
one chemical atom, e.g., sodium-containing, etc., or is
identified as a generic type of inorganic chemical compound,
e.g., alkali metal-containing, etc. The term nonactive as
used herein denotes the absence of any physiological,
pharmacological or biological affect attributed to the
inorganic material.
DESIGNATED ORGANIC ACTIVE INGREDIENT (DOAI) DENOTES
(1) The active ingredient is identified by at least one
chemical atom, e.g., organic phosphorus compound, etc., or
(2) The active ingredient is identified as a generic type of
chemical atom, e.g., alcohol, ether, etc. The term active
denotes the presence of a physiological, pharmacological or
biological affect.
DESIGNATED ORGANIC NONACTIVE INGREDIENT DENOTES
(1) A nonactive ingredient is identified by at least one
chemical atom or (2) the nonactive ingredient is identified
as a generic type of chemical compound, e.g., starch, etc.
The term nonactive denotes the absence of any physiological,
pharmacological or biological affect attributed to the
organic material.
ETHER
Denotes an organic compound having oxygen bonded directly to
two carbon atoms, which carbons cannot be double bonded to
oxygen, sulfur, selenium, or tellurium, or triple bonded to
nitrogen.
FATTY ACID
Denotes an aliphatic monocarboxylic acid having an unbroken
chain of at least seven carbon atoms bonded to the carboxyl
group.
FUSED OR BRIDGED RING SYSTEM
Denotes a ring system having at least two rings which (a)
share with each other two adjacent ring atoms, or (b) share
with each other three or more ring atoms and wherein each
ring having shared atoms is either a heterocyclic ring or a
carbocyclic ring.
HALOGENATED HYDROCARBON
Denotes a compound containing only carbon, hydrogen, and
halogen, or only carbon and halogen.
HETERO RING
Denotes the presence of one or more carbon atoms covalently
bonded in a closed ring with at least one atom of oxygen,
nitrogen, sulfur, selenium or tellurium and having no other
atoms in the ring.
INCLUDING HYDROGENATED
Denotes that a ring system which by definition has ring
unsaturation possesses a degree of saturation which may be
different than the ring system definition would normally
indicate.
KETONE (INCLUDING KETENE)
Denotes an organic compound having the general structure
-C-{C(=O)}[subscrpt]n[end subscrpt] -C- (n is 1 or more) and
wherein[subscrpt] [end subscrpt]the carbon atoms bonded to
the-{C(=O)}[subscrpt]n [end subscrpt]group are not double
bonded to oxygen, sulfur, selenium, or tellurium. Ketone as
used throughout includes ketene.
NONIONIC BONDING
As used in regard to bonding or attachment of specified
moieties denotes the absence of ionic bonding between the
moieties. If the moieties are attached directly, the bonds
between them must be covalent or coordinate. If the moieties
are attached indirectly, each atom of the connecting chain
must be attached by covalent or coordinate bonding to another
atom of the connecting chain or to one of the moieties.
However, the connecting chain may have substituents thereon
which include ionic bonding. Some examples will be given of
compounds which could be classified in a subclass having the
following titles: "Oxygen attached indirectly to the
six-membered hetero ring by nonionic bonding". [figure]
[figure]
POLYCYCLO RING SYSTEM
This term denotes a compound which contains fused or bridged
rings. The polycyclo ring system must contain at least two
rings and each ring of the system must share two or more of
its atoms with another ring of the system. All ring members
must be attached to each other by nonionic bonding. The
polycyclo ring system is usually only a moiety within a
compound. Indents such as bicyclo and tricyclo are meant to
limit the number of rings or cyclos in the polycyclo ring
system to exactly two rings and three rings, respectively.
For polycyclo systems having bridges it should be remembered
that the system is regarded as composed only of the smallest
number of smallest rings that will account for all atoms and
valences. This is in accord with the nomenclature employed
by The Ring Index. Second Edition, (1960). [figure]
[figure] [figure] [figure]
SPIRO AND SPIRO RING SYSTEM
These terms denote the sharing of one common ring member only
by exactly two rings. The following two structures are
illustrative: [figure] [figure]
TRICYCLO RING SYSTEM
This term denotes a polycyclo ring system which contains
exactly three rings.
SUBCLASSES
Subclass:
1
![[Patents]](../gifs/ps.gif)
DESIGNATED ORGANIC ACTIVE INGREDIENT CONTAINING (DOAI):
Subject matter under Class 424 definition which contains a
designated organic active ingredient, e.g., coal tar, coal
tar oil, etc.
(1) Note. See Class Definition, Glossary, for the
definition of "DOAI".
SEE OR SEARCH THIS CLASS, SUBCLASS:
731 for a composition containing creosote or a coal tar
acid.
800 and 801-809, for art collections pertaining to
subclasses 1-21.
SEE OR SEARCH CLASS:
208, Mineral Oils: Processes and Products, subclass 2 for a
coal tar or coal tar oil which has the property of killing,
repelling or preventing the growth of insects, fungi or
bacteria and the process of preparing same.
Subclass:
2
![[Patents]](../gifs/ps.gif)
Peptide containing (e.g., protein, peptones, fibrinogen,
etc.) DOAI:
This subclass is indented under subclass 1. Subject matter
which contains a protein or its reaction product, e.g.,
peptides, peptones, fibrinogen, etc., wherein the protein
molecule is not degraded to the constituent amino-acids.
(1) Note. The term peptide unit used herein is intended to
mean the group N-C-(=O) or beta-alanine.
SEE OR SEARCH THIS CLASS, SUBCLASS:
183 for ergot.
192 for penicillin.
200 for cephalosporins.
SEE OR SEARCH CLASS:
260, Chemistry of Carbon Compounds, subclass 112 for a
protein, per se, of unknown structure and method of preparing
same; and subclass 112.5 for a protein, per se, of known
structure.
930, Peptide or Protein Sequence, 10 for peptide or protein
sequences or four or more amino acids.
Subclass:
3
![[Patents]](../gifs/ps.gif)
Insulin or derivative:
This subclass is indented under subclass 2. Subject matter
identical to the extract of the pancreas, known as insulin or
a derivative thereof, in which neither a peptide chain nor a
disulfide link between chains is broken.
(1) Note. While the position and/or kind of amino acids in
the chain(s) may vary (depending on the animal from which
derived), it appears that insulin contains at least an "A"
chain of 21 acid units linked by disulfide moieties to a "B".
An additional disulfide moiety bridges the 6 and 11
positions of chain A.
SEE OR SEARCH THIS CLASS, SUBCLASS:
110 for an animal extract obtained from the pancreas.
SEE OR SEARCH CLASS:
260, Chemistry of Carbon Compounds, subclass 112.5 for a
polypeptide of known chemical structure, and subclass 112.7
for insulin, per se.
Subclass:
4
![[Patents]](../gifs/ps.gif)
With an additional active ingredient:
This subclass is indented under subclass 3. Subject matter
which contains insulin and an additional active ingredient.
(1) Note. For the subclass an organic potentiator for
insulin is considered an active ingredient.
Subclass:
5
![[Patents]](../gifs/ps.gif)
Iodine containing:
This subclass is indented under subclass 2. Subject matter
in which the peptide moiety contains iodine or the peptide
moiety is reacted with or complexed to iodine containing
compound.
SEE OR SEARCH CLASS:
930, Peptide or Protein Sequence, subclass 22 for peptide or
protein sequences containing an amino acid modified with a
radioactive iodine and subclass 23 for sequences containing
an amino acid modified with a regular iodine.
Subclass:
6
![[Patents]](../gifs/ps.gif)
Heavy metal containing (e.g., hemoglobin, etc.):
This subclass is indented under subclass 2. Subject matter
which contains a heavy metal atom.
(1) Note. See Glossary for a definition of the term heavy
metal.
SEE OR SEARCH CLASS:
260, Chemistry of Carbon Compounds, 113 for known
polypeptide compound containing a heavy metal atom.
930, Peptide or Protein Sequence, subclass 25 for peptide or
protein sequences containing an amino acid modified with a
heavy metal.
Subclass:
7
![[Patents]](../gifs/ps.gif)
Phosphorus containing:
This subclass is indented under subclass 2. Subject matter
which contains phosphorus in the peptide compound.
Subclass:
8
![[Patents]](../gifs/ps.gif)
Glycoprotein (carbohydrate containing):
This subclass is indented under subclass 2. Subject matter
which contains a carbohydrate or derivative thereof attached
to the peptide.
Subclass:
9
![[Patents]](../gifs/ps.gif)
Cyclopeptide:
This subclass is indented under subclass 2. Subject matter
wherein the amino acid chain forms a cyclic structure; said
cyclo structures can be formed by peptide bonding, disulfide
bonding, hydrocarbon bonding or other types of connection
that define the cyclo structures as having at least a
dipeptide as an integral part thereof.
SEE OR SEARCH CLASS:
930, Peptide or Protein Sequence, subclass 260 for peptides
or proteins with intrachain cysteine-cysteine bridges and
subclass 270 for other cyclic peptides or proteins.
Subclass:
10
![[Patents]](../gifs/ps.gif)
Bicyclic:
This subclass is indented under subclass 9. Subject matter
wherein a compound has two cyclic groups containing an amino
acid chain.
Subclass:
11
![[Patents]](../gifs/ps.gif)
Monocyclic:
This subclass is indented under subclass 9. Subject matter
wherein a compound has only one cyclic group containing an
amino acid chain.
Subclass:
12
![[Patents]](../gifs/ps.gif)
25 or more peptide repeating units in known peptide chain
structure:
This subclass is indented under subclass 2. Subject matter
wherein a peptide chain has 25 or more peptide units in an
uninterrupted chain.
Subclass:
13
![[Patents]](../gifs/ps.gif)
16 to 24 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains as uninterrupted peptide chain of 16 to 24
peptide units.
Subclass:
14
![[Patents]](../gifs/ps.gif)
12 to 15 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains an uninterrupted peptide chain of 12 to 15
peptide units.
Subclass:
15
![[Patents]](../gifs/ps.gif)
9 to 11 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains an uninterrupted peptide chain of 9 to 11
peptide units.
Subclass:
16
![[Patents]](../gifs/ps.gif)
7 or 8 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains an uninterrupted peptide chain of 7 or 8
peptide units.
Subclass:
17
![[Patents]](../gifs/ps.gif)
5 or 6 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains an uninterrupted peptide chain 5 or 6 peptide
units.
Subclass:
18
![[Patents]](../gifs/ps.gif)
3 or 4 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains an uninterrupted peptide chain of 3 or 4
peptide units.
Subclass:
19
![[Patents]](../gifs/ps.gif)
2 peptide repeating units in known peptide chain:
This subclass is indented under subclass 2. Subject matter
which contains an uninterrupted peptide chain of 2 peptide
units.
Subclass:
20
![[Patents]](../gifs/ps.gif)
Guanidine containing:
This subclass is indented under subclass 19. Subject matter
wherein the peptide compound contains the guanidine group.
Subclass:
21
![[Patents]](../gifs/ps.gif)
Produced by or extracted from animal tissue:
This subclass is indented under subclass 2. Subject matter
which is derived from animal material.
SEE OR SEARCH THIS CLASS, SUBCLASS:
800 and 801-809, for art collections pertaining to
subclasses 1-21.
Subclass:
22
![[Patents]](../gifs/ps.gif)
Lignin or derivative DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the organic active ingredient is lignin or a reaction
derivative thereof, e.g., lignin sulfonate, etc.
(1) Note. Lignin is a noncarbohydrate, polymeric substance
found in wood. It is isolated directly from wood or wood
products or from the treatment of wood, e.g., waste sulfite
liquor or black liquor. The structure of the lignin monomer
is not completely known.
Subclass:
23
![[Patents]](../gifs/ps.gif)
Carbohydrate (i.e., saccharide radical containing) DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the organic active ingredient is a saccharide or
polysaccharide, the monomeric saccharide radical units of
which contain at least five carbon atoms, or their reaction
products wherein the carbon skeleton of the saccharide or
polysaccharide of the unit is not destroyed.
(1) Note. Included herein is cellulose, cellulose
derivatives, starch, starch derivatives, tannins,
O-glycosides, N-glycosides and S-glycosides.
(2) Note. Alcohols and acids corresponding to carbohydrates
are excluded.
(3) Note. Cascara sagrada is excluded herefrom and is
classified with plant extracts. See Search Notes below.
SEE OR SEARCH THIS CLASS, SUBCLASS:
251 for a composition containing riboflavin DOAI.
SEE OR SEARCH CLASS:
424, Drug, Bio-Affecting and Body Treating Compositions,
subclass 195.1 for plant extracts
Subclass:
24
![[Patents]](../gifs/ps.gif)
S-glycoside:
This subclass is indented under subclass 23. Subject matter
wherein the saccharide is a thioacetal derivative of a cyclic
form of sugars in which the hydrogen atom of the
hemithioacetal sulfhydryl group has been replaced by an
alkyl, aralkyl or aryl group.
(1) Note. A S-glycoside is a compound having a sugar moiety
connected to an aglycone moiety via sulfur.
(2) Note. An aglycone is a noncarbohydrate material, e.g.,
benzene, indoxyl, alkyl, anthracene, etc.
(3) Note. The cyclic sugars referred to in the definition
are normally pyranoses or furanoses.
(4) Note. Glycosides derived from aldoeses are referred to
as aldosides, and those ketoses are ketosides.
Subclass:
25
![[Patents]](../gifs/ps.gif)
O-glycoside:
This subclass is indented under subclass 23. Subject matter
wherein the saccharide is an acetal derivative of a cyclic
form of sugars in which the hydrogen atom of the hemiacetal
hydroxyl has been replaced by an alkyl, aralkyl or aryl
group.
(1) Note. An O-glycoside is a compound having a sugar
moiety connected to an aglycone moiety via oxygen.
Subclass:
26
![[Patents]](../gifs/ps.gif)
Cyclopentanohydrophenanthrene ring system:
This subclass is indented under subclass 25. Subject matter
wherein an aglycone moiety of the glycoside contains a
cyclopentanohydrophenanthrene nucleus, i.e., [figure]
Subclass:
27
![[Patents]](../gifs/ps.gif)
Oxygen of the saccharide radical bonded directly to a
nonsaccharide hetero ring or a polycyclo ring system which
contains a nonsaccharide hetero ring:
This subclass is indented under subclass 25. Subject matter
wherein a nonsaccharide hetero ring or a fused or bridged
ring system which contains a nonsaccharide hetero ring is
attached to an oxygen of the saccharide radical, e.g.,
[figure]
Subclass:
28
![[Patents]](../gifs/ps.gif)
The hetero ring has 8 or more ring carbons:
This subclass is indented under subclass 27. Subject mater
wherein the nonsaccharide hetero ring has eight or more ring
carbon members.
Subclass:
29
![[Patents]](../gifs/ps.gif)
The hetero ring has exactly 13 ring carbons (e.g.,
erythromycin, etc.):
This subclass is indented under subclass 28. Subject matter
wherein the nonsaccharide hetero ring has exactly 13 carbon
atoms, e.g., erythromycin, etc.
Subclass:
30
![[Patents]](../gifs/ps.gif)
The hetero ring has exactly 15 ring carbons:
This subclass is indented under subclass 28. Subject matter
wherein the nonsaccharide hetero ring has exactly 15 carbon
atoms.
Subclass:
31
![[Patents]](../gifs/ps.gif)
The hetero ring has 20 or more ring carbons (e.g., nystatin,
etc.):
This subclass is indented under subclass 28. Subject matter
wherein the nonsaccharide hetero ring has 20 or more ring
carbon atoms, e.g., nystatin, etc.
Subclass:
32
![[Patents]](../gifs/ps.gif)
Oxygen of the saccharide radical bonded to a nonsaccharide
hetero ring by acyclic carbon bonding:
This subclass is indented under subclass 25. Subject matter
wherein a hetero ring or polycyclo ring system which contains
a nonsaccharide hetero ring is directly linked to an oxygen
of the saccharide radical directly through only acyclic
carbon bonding, e.g., [figure]
Subclass:
33
![[Patents]](../gifs/ps.gif)
Oxygen of the saccharide radical bonded directly to a polyclo
ring system of three or more carbocyclic rings:
This subclass is indented under subclass 25. Subject matter
wherein the oxygen of the saccharide radical is directly
bonded to a polycyclo ring system of three or more
carbocyclic rings.
Subclass:
34
![[Patents]](../gifs/ps.gif)
Oxygen of the saccharide radical bonded directly to a
polycyclo ring system of four carbocyclic rings (e.g.,
daunomycin, etc.):
This subclass is indented under subclass 33. Subject matter
wherein the oxygen of the saccharide radical is directly
bonded to a polycyclo ring system of exactly four carbocyclic
rings.
Subclass:
35
![[Patents]](../gifs/ps.gif)
Oxygen of the saccharide radical bonded directly to a
cyclohexyl ring:
This subclass is indented under subclass 25. Subject matter
wherein a cyclohexyl radical is bonded directly to an oxygen
of the saccharide radical, e.g., [figure]
Subclass:
36
![[Patents]](../gifs/ps.gif)
Two or more nitrogen atoms bonded directly to the cyclohexyl
ring:
This subclass is indented under subclass 35. Subject matter
wherein two or more nitrogen atoms are bonded directly to the
cyclohexyl radical, e.g., [figure]
Subclass:
37
![[Patents]](../gifs/ps.gif)
The nitrogen atoms are in N-C(=N)-N groups (e.g,
streptomycin, etc.):
This subclass is indented under subclass 36. Subject matter
wherein all the nitrogen atoms which are bonded directly to
the cyclohexyl group are part of a N-C(=N)-N group, e.g.,
[figure] [caption], etc.
Subclass:
38
![[Patents]](../gifs/ps.gif)
Two saccharide radicals bonded through only oxygen to
adjacent ring carbons of the cyclohexyl ring:
This subclass is indented under subclass 36. Subject matter
wherein the cyclohexyl radical is separately, independently
and directly bonded through only oxygen of two saccharide
radicals at adjacent ring carbons, e.g., [figure] [caption],
etc.
Subclass:
39
![[Patents]](../gifs/ps.gif)
Three or more saccharide radicals (e.g., neomycin, etc.):
This subclass is indented under subclass 38. Subject matter
wherein the cyclohexyl radical is bonded directly or
indirectly to three or more saccharide radicals, e.g.,
[figure] [caption], etc.
Subclass:
40
![[Patents]](../gifs/ps.gif)
Two saccharide radicals bonded through only oxygen to 4- and
6- positions of the cyclohexyl ring:
This subclass is indented under subclass 36. Subject matter
wherein the cyclohexyl radical is separately, independently
and directly bonded through only oxygen of two saccharide
radicals at the 4- and 6- position carbons of the cyclohexyl
ring, e.g., [figure] [caption], etc.
Subclass:
41
![[Patents]](../gifs/ps.gif)
Kanamycin or derivative:
This subclass is indented under subclass 40. Subject matter
wherein the organic active ingredient is Kanamycin or a
derivative thereof, i.e., as illustrated below, wherein R is
NH[subscrpt]2[end subscrpt] and R' is NH[subscrpt]2[end
subscrpt] or OH. [figure] [caption]Kanosamin,
deoxystreptamine
Subclass:
42
![[Patents]](../gifs/ps.gif)
N-glycoside:
This subclass is indented under subclass 23. Subject matter
wherein the saccharide is a glycosidic derivative or the
cyclic form of saccharides or polysaccharides in which an
aglycone portion is attached through nitrogen to the
saccharide moiety by substituting it for the hemiacetal
hydroxyl of the sugar.
(1) Note. The aglycone can be noncyclic.
Subclass:
43
![[Patents]](../gifs/ps.gif)
Nitrogen containing hetero ring:
This subclass is indented under subclass 42. Subject matter
wherein the aglycone portion contains a nitrogen containing
hetero ring.
Subclass:
44
![[Patents]](../gifs/ps.gif)
Polynucleotide (e.g., RNA, DNA, etc.):
This subclass is indented under subclass 43. Subject matter
which has the following structure, illustrated below, wherein
n is a whole number equal or greater than two, R' is H or OH
and R" is purine or pyrimidine or a substituted purine or
pyrimidine. [figure]
(1) Note. Substituted pyrimidine or purine includes only
those derivatives which are substituted on rather than in the
respective ring position, i.e., illustrated below, is present
in the structure. The internal ring bonding may be altered
by tautomerism or by the addition of substituents without
excluding a compound from this subclass. [figure] [caption]Or
[figure]
SEE OR SEARCH CLASS:
536, Organic Compounds, appropriate subclasses for
nucleosides, nucleotides and polynucleotides like RNA or DNA
compounds as well as chemical methods for synthesizing these
compounds. Search specifically 23.1 for fragments of DNA
which could have utility in recombinant processes or gene
therapy and subclasses 26.4+ for vitamin B-12 and its
derivatives.
Subclass:
45
![[Patents]](../gifs/ps.gif)
Purines (including hydrogenated) (e.g., adenine, guanine,
etc.):
This subclass is indented under subclass 43. Subject matter
wherein the hetero ring is a purine, as illustrated below, or
substituted purine. [figure]
Subclass:
46
![[Patents]](../gifs/ps.gif)
Adenosine or derivative:
This subclass is indented under subclass 45. Subject matter
wherein the compound is adenosine, illustrated below, or
derivative thereof. [figure]
Subclass:
47
![[Patents]](../gifs/ps.gif)
Phosphorus containing:
This subclass is indented under subclass 46. Subject matter
wherein the adenosine or derivative thereof contains
phosphorus.
Subclass:
48
![[Patents]](../gifs/ps.gif)
Phosphorus containing:
This subclass is indented under subclass 45. Subject matter
wherein the purine compound contains phosphorus.
Subclass:
49
![[Patents]](../gifs/ps.gif)
Pyrimidines (including hydrogenated) (e.g., cytosine, etc.):
This subclass is indented under subclass 43. Subject matter
wherein the hetero ring is a pyrimidine, as illustrated
below, or substituted pyrimidine.
(1) Note. The structure below shows the position numbering
used for 1, 3-diazines. [figure]
Subclass:
50
![[Patents]](../gifs/ps.gif)
2, 4-diketone pyrimidine or derivative (e.g., uracil, etc.):
This subclass is indented under subclass 49. Subject matter
wherein oxygen atoms are directly double bonded to the 2 and
4 positions of the pyrimidine ring, e.g., [figure] [caption],
etc.
Subclass:
51
![[Patents]](../gifs/ps.gif)
Phosphorus containing:
This subclass is indented under subclass 50. Subject matter
wherein the 2, 4-diketone pyrimidine compound contains
phosphorus.
Subclass:
52
![[Patents]](../gifs/ps.gif)
Phosphorus containing (e.g., vitamin B12, etc.):
This subclass is indented under subclass 43. Subject matter
which contains phosphorus.
Subclass:
53
![[Patents]](../gifs/ps.gif)
Disaccharide:
This subclass is indented under subclass 23. Subject matter
wherein the organic active ingredient contains two saccharide
radicals bonded via a glycosidic linkage and which on
hydrolysis yields two units of monosaccharides (e.g.,
sucrose, lactose, maltose, etc.).
Subclass:
54
![[Patents]](../gifs/ps.gif)
This subclass is indented under subclass 23. Subject matter
wherein the organic active ingredient contains more than two
saccharide radicals directly or indirectly bonded together.
Subclass:
55
![[Patents]](../gifs/ps.gif)
Chitin or derivative:
This subclass is indented under subclass 54. wherein the
polysaccharide has the following repeating units: [figure]
[caption]Repeating unit of chitin.
Subclass:
56
![[Patents]](../gifs/ps.gif)
Heparin or derivative:
This subclass is indented under subclass 54. Subject matter
wherein the polysaccharide has the following repeating unit,
illustrated below, wherein the degree of sulfation of the
individual components in the polysaccharide chain, and
derivatives thereof.
(1) Note. Heparin is a substance which can be found in
various tissues of mammals, especially the lung, spleen,
liver and muscle, and has been used medicinally for
coagulation of blood and metabolism of lipids.
Subclass:
57
![[Patents]](../gifs/ps.gif)
Cellulose or derivative:
This subclass is indented under subclass 54. Subject matter
wherein the polysaccharide consists of repeating glucose
units having the following structure: [figure]
Subclass:
58
![[Patents]](../gifs/ps.gif)
Dextrin or derivative:
This subclass is indented under subclass 54. Subject matter
wherein the polysaccharide consists of various gummy
polysaccharides produced by thermal or acid degradation of
starch, and derivatives of such compounds.
(1) Note. Dextrins are carbohydrates, intermediate between
starch and sugars. Degradation of dextrins yields maltose
and glucose.
(2) Note. Derivatives of dextrins which remain gummy
polysaccharides are classified herein.
Subclass:
59
![[Patents]](../gifs/ps.gif)
Dextran or derivative:
This subclass is indented under subclass 54. wherein the
polysaccharide is composed of D-glucose units which are
linked by 1, 6 glucosidic bonds.
(1) Note. Dextrin and dextrine are not variant spelling of
"Dextran", instead they are respectively a starch hydrolysis
product and a variant spelling of dextrin.
(2) Note. Controlled hydrolysis of native dextran yields
clinical dextran of lower molecular weight which is useful as
a blood plasma substitute.
Subclass:
60
![[Patents]](../gifs/ps.gif)
Starch or derivative:
This subclass is indented under subclass 54. Subject matter
wherein the polysaccharide has amylose and amylopectin as
their main components.
(1) Note. Starches are heterogeneous in that the amylose
and amylopectin occur in different ratios to each other.
(2) Note. Starches yield dextrins upon extensive thermal of
acid degradation and yield glucose upon completed
hydrolysis.
Subclass:
61
![[Patents]](../gifs/ps.gif)
Tri- or tetrasaccharide:
This subclass is indented under subclass 23. Subject matter
wherein a glucose moiety is substituted with one or more
amino groups, or derivative thereof.
Subclass:
62
![[Patents]](../gifs/ps.gif)
Silicon containing DOAI:
This subclass is indented under subclass 23. Subject matter
wherein a glucose moiety is substituted with one or more
amino groups, or derivative thereof.
Subclass:
63
![[Patents]](../gifs/ps.gif)
Silicon containing DOAI:
This subclass is indented under subclass 1. Subject matter
in which the organic active ingredient contains silicon.
Subclass:
64
![[Patents]](../gifs/ps.gif)
Boron containing DOAI:
This subclass is indented under subclass 1. in which the
organic active ingredient contains boron.
Subclass:
65
![[Patents]](../gifs/ps.gif)
Pyrethrum plant derived material or plant derive rotenone
compound containing DOAI:
This subclass is indented under subclass 1. Subject matter
which contains pyrethrum plant derived material or plant
derived rotenone compound containing material, e.g., ground
pyrethrum flowers or extract of cube root or derris root,
etc.
(1) Note. This subclass does not contain chemically
identified derivatives of naturally occurring pyrethrum plant
derived material or plant derived rotenone containing
material since such derivatives are classified on the basis
of the chemical structure.
(2) Note. Synthetically produced active compounds which
would be identical with the active constituents of pyrethrum
or rotenone containing plant such as derris root, cube root
are not classified herein but are classified of the chemical
structure of the synthetically produced compound. See, for
example, subclass 531 for allethrins.
(3) Note. The active constituents of pyrethrum includes
pyrethrins I and II, cinerins I and II and jasmolins I and
II.
Subclass:
66
![[Patents]](../gifs/ps.gif)
With heterocyclic compound:
This subclass is indented under subclass 65. Subject matter
which contains a heterocyclic compound in addition to the
pyrethrum derived material or plant derived rotenone
compound.
Subclass:
67
![[Patents]](../gifs/ps.gif)
Methlenedioxyphenyl group containing (e.g., piperonyl
butoxide, etc.):
This subclass is indented under subclass 66. Subject matter
which contains methylenedioxyphenyl group, e.g., [figure]
[caption], etc.
Subclass:
68
![[Patents]](../gifs/ps.gif)
With carboxylic acid ester:
This subclass is indented under subclass 65. Subject matter
which contains a carboxylic acid ester in addition to the
pyrethrum derived material or plant derived rotenone
compound.
Subclass:
69
![[Patents]](../gifs/ps.gif)
With carboxylic acid metal salt:
This subclass is indented under subclass 65. Subject matter
which contains a carboxylic acid metal salt in addition to
the pyrethrum derived material or plant derived rotenone
compound.
Subclass:
70
![[Patents]](../gifs/ps.gif)
With organic nitrogen containing compound:
This subclass is indented under subclass 65. Subject matter
which contains a nitrogen containing organic compound in
addition to the pyrethrum derived material or plant derived
rotenone compound.
Subclass:
71
![[Patents]](../gifs/ps.gif)
Sulfur containing organic nitrogen compound:
This subclass is indented under subclass 70. Subject matter
wherein the nitrogen containing organic compound contains
sulfur.
Subclass:
72
![[Patents]](../gifs/ps.gif)
With organic oxygen containing compound:
This subclass is indented under subclass 65. Subject matter
which contains oxygen containing organic compound in addition
to the pyrethrum derived material or plant derived rotenone
compound.
Subclass:
73
![[Patents]](../gifs/ps.gif)
Phosphorus or halogen containing organic oxygen compound:
This subclass is indented under subclass 72. Subject matter
wherein the oxygen containing organic compound contains
phosphorus or halogen.
Subclass:
74
![[Patents]](../gifs/ps.gif)
With hydrocarbon or halohydrocarbon:
This subclass is indented under subclass 65. Subject matter
which contains hydrocarbon or halohydrocarbon in addition to
the pyrethrum derived material or plant derived rotenone
compound.
Subclass:
75
![[Patents]](../gifs/ps.gif)
Phosphorus containing other than solely as part of an
inorganic ion in an addition salt DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the organic active ingredient contains a phosphorus
atom.
(1) Note. Inorganic phosphorus salts of the organic active
ingredient are excluded herefrom and classified with the
active moiety.
Subclass:
76
![[Patents]](../gifs/ps.gif)
Amine addition salt of organic phosphorus containing acid:
This subclass is indented under subclass 75. Subject matter
wherein the organic active ingredient is an amine addition
salt of the phosphorus compound, wherein said salt forming
group is the nitrogen atom of said amine, e.g., [figure]
[caption], etc.
Subclass:
77
![[Patents]](../gifs/ps.gif)
Inner salt (e.g., betaine, etc.):
This subclass is indented under subclass 75. Subject matter
wherein the organic active ingredient is an inner salt, e.g.,
[figure] [figure] [caption], etc.
Subclass:
78
![[Patents]](../gifs/ps.gif)
Lecithins:
This subclass is indented under subclass 77. Subject matter
wherein the inner salt contains the following
structurewherein R is an organic radical. [figure] [caption],
etc.
Subclass:
79
![[Patents]](../gifs/ps.gif)
Nitrogen containing hetero ring:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains a
heterocyclic ring containing nitrogen as a hetero atom.
Subclass:
80
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having a ring nitrogen in the system:
This subclass is indented under subclass 79. Subject matter
in which the organo-phosphorus compound contains a polycyclo
ring system (bridged or fused), e.g., [figure] [caption],
etc.
Subclass:
81
![[Patents]](../gifs/ps.gif)
Nonshared hetero atoms in at least two rings of the polycyclo
ring system:
This subclass is indented under subclass 80. Subject matter
in which the organo-phosphorus compound contains a polycyclo
ring system which contains nonshared hetero atoms in at least
two rings of the polycyclo ring systems, e.g., [figure]
[caption], etc.
Subclass:
82
![[Patents]](../gifs/ps.gif)
Quinolinyl or isoquinolinyl (including hydrogenated):
This subclass is indented under subclass 80. Subject matter
in which the organo-phosphorus compound contains a quinolinyl
or isoquinolinyl group, (including hydrogenated).
Subclass:
83
![[Patents]](../gifs/ps.gif)
Hetero ring is three-membered consisting of one nitrogen and
two carbons:
This subclass is indented under subclass 79. Subject matter
in which the organo-phosphorus compound contains a
three-membered heterocyclic ring which contains one nitrogen
and two carbons.
Subclass:
84
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered consisting of three nitrogens and
three carbons:
This subclass is indented under subclass 79. Subject matter
in which the organo-phosphorus compound contains a
six-membered heterocyclic ring which consists of three
nitrogens and three carbons.
Subclass:
85
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered consisting of two nitrogens and
four carbons:
This subclass is indented under subclass 79. Subject matter
in which the organo-phosphorus compound contains a
six-membered heterocyclic ring which consists of two
nitrogens and four carbons.
Subclass:
86
![[Patents]](../gifs/ps.gif)
Nitrogen atoms occupy 1 and 3- positions:
This subclass is indented under subclass 85. Subject matter
wherein the nitrogen atoms are at the 1- and 3- position of
the six member ring, i.e., 1, 3-diazines.
Subclass:
87
![[Patents]](../gifs/ps.gif)
PX- bonded directly to 1, 3-diazine at 2-position (X is
chalcogen):
This subclass is indented under subclass 86. Subject matter
in which a PX- is bonded directly to the 1,3-diazine at the
2-position. (X is chalcogen), e.g., [figure] [caption],
etc.
Subclass:
88
![[Patents]](../gifs/ps.gif)
Two or more PX- groups attached to the same 1,3-diazine (X is
chalcogen):
This subclass is indented under subclass 86. in which at
least two PX's are bonded directly to the 1,3-diazine moiety,
e.g., [figure] [caption], etc.
Subclass:
89
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered and includes only one ring
nitrogen:
This subclass is indented under subclass 79. Subject matter
in which the organo-phosphorus compound contains a
heterocyclic ring which has six members and includes only one
therein, e.g., [figure] [caption], etc.
Subclass:
90
![[Patents]](../gifs/ps.gif)
Chalcogen in the six-membered hetero ring:
This subclass is indented under subclass 89. Subject matter
in which the organo-phosphorus compound contains a
six-membered heterocyclic ring which also contains a
chalcogen atom as well as the nitrogen, e.g., [figure]
[caption], etc.
Subclass:
91
![[Patents]](../gifs/ps.gif)
Hetero ring is five-membered:
This subclass is indented under subclass 79. Subject matter
in which the organo-phosphorus compound contains a
heterocyclic moiety which has five members.
Subclass:
92
![[Patents]](../gifs/ps.gif)
Two or more hetero atoms in the five-membered ring:
This subclass is indented under subclass 91. Subject matter
in which the organo-phosphorus compound contains a
five-membered heterocyclic moiety which contains two or more
hetero atoms.
Subclass:
93
![[Patents]](../gifs/ps.gif)
Triazoles (including hydrogenated):
This subclass is indented under subclass 92. Subject matter
in which the organo-phosphorus compound contains a
five-membered heterocyclic moiety which consists of three
nitrogens and two carbons.
Subclass:
94
![[Patents]](../gifs/ps.gif)
Diazoles (including hydrogenated):
This subclass is indented under subclass 92. Subject matter
in which the organo-phosphorus compound contains a
five-membered heterocyclic moiety which contains two
nitrogens and three carbons.
Subclass:
95
![[Patents]](../gifs/ps.gif)
Sulfur containing hetero ring:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains a
heterocyclic ring which contains at least one sulfur atom as
a ring member.
Subclass:
96
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 95. Subject matter
in which the organo-phosphorus compound contains a bridged or
fused ring system which has a heterocyclic sulfur containing
ring as one of the cyclos.
Subclass:
97
![[Patents]](../gifs/ps.gif)
Two or more sulfurs in the hetero ring:
This subclass is indented under subclass 95. Subject matter
in which the organo-phosphorus compound contains at least two
sulfur atoms as ring members.
Subclass:
98
![[Patents]](../gifs/ps.gif)
Oxygen in the hetero ring:
This subclass is indented under subclass 95. Subject matter
in which the organo-phosphorus compound contains a
heterocyclic ring which contains at least one sulfur atom and
at least one oxygen atom as ring members.
Subclass:
99
![[Patents]](../gifs/ps.gif)
Oxygen containing hetero ring:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains at least one
oxygen atom as a ring member.
Subclass:
100
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 99. Subject matter
in which the organo-phosphorus compound contains a fused or
bridged ring system which contains a heterocyclic
oxygen-containing ring as one of the cyclos.
Subclass:
101
![[Patents]](../gifs/ps.gif)
Two or more oxygen in the hetero ring:
This subclass is indented under subclass 99. Subject matter
in which the organo-phosphorus compound contains a
heterocyclic ring which contains at least two oxygen atoms as
ring members.
Subclass:
102
![[Patents]](../gifs/ps.gif)
Two or more phosphorus atoms directly or indirectly bonded
together by only covalent bonds:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains at least two
nonionically bonded phosphorus atoms.
(1) Note. Organic phosphorus salts and complexes of a
phosphorus containing compound and other compounds are
excluded unless the phosphorus containing moiety has at least
two nonionically bonded phosphorus atoms, e.g., [figure]
[caption], etc.
Subclass:
103
![[Patents]](../gifs/ps.gif)
Phosphorus acid ester of polyhydric alcohol or
thioalcohol(e.g., P-X-R-X-P group, etc., wherein X is
chalcogen and R is the residue of the polyhydric alcohol or
thioalcohol):
This subclass is indented under subclass 102. Subject matter
in which the organo-phosphorus compound is a phosphorus acid
ester of a polyhydric alcohol or thioalcohol, e.g., P-X-(R)
XP group, etc., wherein X is chalcogen and R is the residue
of a polyhydric alcohol.
Subclass:
104
![[Patents]](../gifs/ps.gif)
Benzene ring in the alcohol moiety:
This subclass is indented under subclass 103. Subject matter
in which the polyphosphorus compound corresponds to the
structure -P-X-(R)-X-P-, wherein R is the residue of a
polyhydric alcohol which is aromatic in nature (i.e.,
contains a benzene ring and wherein X is chalcogen).
Subclass:
105
![[Patents]](../gifs/ps.gif)
Phosphorus is part of a ring:
This subclass is indented under subclass 102. Subject matter
in which a phosphorus atom is part of a ring, e.g., [figure]
[caption], etc.
Subclass:
106
![[Patents]](../gifs/ps.gif)
P-O-P or P-S-P containing (e.g., anhydrides, etc.):
This subclass is indented under subclass 102. Subject matter
which contains a polyphosphorus compound wherein two
phosphorus atoms are linked to each other through a single
oxygen or sulfur (i.e., P-O-P OR P-S-P).
Subclass:
107
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 102. Subject matter
in which the phosphorus compound contains a benzene ring.
Subclass:
108
![[Patents]](../gifs/ps.gif)
Acyclic and contains at least one carbon atom between the
phosphorus atoms:
This subclass is indented under subclass 102. Subject matter
in which the phosphorus compound is acyclic and contains at
least one carbon between the phosphorus atoms.
Subclass:
109
![[Patents]](../gifs/ps.gif)
P-X-X containing (X is chalcogen):
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound has a single
phosphorus atom linked directly to a chalcogen atom which in
turn is linked directly to another chalcogen atom, e.g., as
illustrated below, wherein X is chalcogen. [figure]
[caption], etc.
Subclass:
110
![[Patents]](../gifs/ps.gif)
Phosphorus is part of a ring:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains the
phosphorus atom as part of a ring, e.g., [figure] [caption],
etc.
Subclass:
111
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the phosphorus containing ring
as one of the cyclos:
This subclass is indented under subclass 110. Subject matter
in which the organo-phosphorus compound contains a fused ring
system or bridged ring system of which the phosphorus
containing ring is a part, e.g., [figure] [caption], etc.
Subclass:
112
![[Patents]](../gifs/ps.gif)
Cyano or isocyano containing:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains at least one
nitrile or isonitrile radical bonded to a carbon.
Subclass:
113
![[Patents]](../gifs/ps.gif)
Cyano or isocyano bonded directly to a benzene ring:
This subclass is indented under subclass 1. Subject matter
in which the nitrile or isonitrile radical bonded to a
benzene ring.
Subclass:
114
![[Patents]](../gifs/ps.gif)
Nitrogen, other than nitro or nitroso, bonded indirectly to
phosphorus:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains a nitrogen,
other than nitro or nitroso, which is not directly bonded to
the phosphorus atom, e.g., [figure] [figure] [caption], etc.
Subclass:
115
![[Patents]](../gifs/ps.gif)
N-C(=X)-N containing (S is chalcogen):
This subclass is indented under subclass 114. Subject matter
in which the organo-phosphorus compound contains the radical
NN wherein X is chalcogen.
Subclass:
116
![[Patents]](../gifs/ps.gif)
Sulfur single bonded directly to nitrogen:
This subclass is indented under subclass 114. Subject matter
in which the organo-phosphorus compound contains a sulfur
atom which is directly bonded to a nitrogen by a single
bond.
Subclass:
117
![[Patents]](../gifs/ps.gif)
N-(=O)S(=O) containing (i.e., sulfonamides):
This subclass is indented under subclass 116. Subject matter
in which the organo-phosphorus compound contains the
sulfonamido group, e.g., [figure] [figure] [caption], etc.
Subclass:
118
![[Patents]](../gifs/ps.gif)
Phosphorus single bonded directly to nitrogen:
This subclass is indented under subclass 114. Subject matter
in which the organo-phosphorus compound contains a nitrogen
which is directly bonded to a phosphorus atom by a single
bond, e.g., [figure] [caption], etc.
Subclass:
119
![[Patents]](../gifs/ps.gif)
C(=O)N containing:
This subclass is indented under subclass 114. Subject matter
in which the organo-phosphorus compound contains an amido
group, e.g., [figure] [caption], etc.
Subclass:
120
![[Patents]](../gifs/ps.gif)
C=O other than as ketone or aldehyde, attached directly or
indirectly to phosphorus:
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound contains a carbonyl
group, other than as ketone or aldehyde, e.g., [figure]
[caption], etc.
Subclass:
121
![[Patents]](../gifs/ps.gif)
Plural C=O groups, other than as ketone or aldehyde:
This subclass is indented under subclass 120. Subject matter
wherein the organo-phosphorus compound contains two C=O
groups which are other than a ketone or aldehyde, e.g.,
[figure] [caption], etc.
Subclass:
122
![[Patents]](../gifs/ps.gif)
Malathion:
This subclass is indented under subclass 121. Subject matter
wherein the organo-phosphorus compound is malathion, i.e.,
[figure] [caption], etc.
Subclass:
123
![[Patents]](../gifs/ps.gif)
With N-C(=O)-O containing compound:
This subclass is indented under subclass 122. Subject matter
wherein another compound is present, along with malathion,
which has the N(C=O)-O group therein, e.g., [figure]
[caption], etc.
Subclass:
124
![[Patents]](../gifs/ps.gif)
C=O, other than as ketone or aldehyde, attached to a benzene
ring:
This subclass is indented under subclass 120. Subject Matter
wherein the organo-phosphorus compound contains a C=O group
other than as ketone or aldehyde attached directly to a
benzene ring, e.g., [figure] [caption], etc.
Subclass:
125
![[Patents]](../gifs/ps.gif)
Ketone or aldehyde containing:
This subclass is indented under subclass 75. Subject matter
wherein the organo-phosphorus compound contains at least one
carbonyl group in the form of an aldehyde or ketone.
Subclass:
126
![[Patents]](../gifs/ps.gif)
Sulfur not bonded directly to phosphorus:
This subclass is indented under subclass 126. Subject matter
in which the organo-phosphorus compound contains sulfur and
wherein said sulfur is not bonded directly to the phosphorus
atom.
Subclass:
127
![[Patents]](../gifs/ps.gif)
Thioether, sulfoxide or sulfone:
This subclass is indented under subclass 126. Subject matter
in which the organo-phosphorus compound contains sulfur in
the form of a thioether, sulfoxide or sulfone group.
(1) Note. This subclass contains the groups: C-S-C; C- C,
and C- C
Subclass:
128
![[Patents]](../gifs/ps.gif)
Sulfur bonded directly to a benzene ring:
This subclass is indented under subclass 127. Subject matter
wherein the sulfur is directly bonded to a carbon of a
benzene ring.
Subclass:
129
![[Patents]](../gifs/ps.gif)
Oxygen bonded directly to a carbon or hydrogen and wherein
the oxygen is not bonded directly to phosphorus:
This subclass is indented under subclass 75. Subject matter
wherein the organo-phosphorus compound contains an oxygen
which is bonded directly to a carbon or hydrogen and wherein
the oxygen is not bonded to phosphorus, e.g ., [figure]
[figure] [caption], etc.
Subclass:
130
![[Patents]](../gifs/ps.gif)
The oxygen is bonded directly to a benzene ring:
This subclass is indented under subclass 129. Subject matter
wherein the oxygen therein is directly bonded to a benzene
ring.
Subclass:
131
![[Patents]](../gifs/ps.gif)
Nitro group bonded to a carbon:
This subclass is indented under subclass 75. Subject matter
wherein the organo-phosphorus compound contains at least one
nitro substituent bonded to a carbon.
Subclass:
132
![[Patents]](../gifs/ps.gif)
Nitro group is directly bonded to a benzene ring which
benzene ring is either bonded directly bonded to phosphorus
or indirectly bonded to phosphorus through a chalcogen:
This subclass is indented under subclass 131. Subject matter
wherein the nitro is directly attached to a benzene ring
which is directly bonded to phosphorus, or indirectly bonded
to phosphorus through a chalcogen, e.g., [figure] [caption],
etc.
Subclass:
133
![[Patents]](../gifs/ps.gif)
Two or more such benzene rings:
This subclass is indented under subclass 132. Subject matter
wherein two or more such nitro substituted benzene rings are
present.
Subclass:
134
![[Patents]](../gifs/ps.gif)
Acyclic carbon to carbon unsaturation:
This subclass is indented under subclass 75. Subject matter
wherein the organo-phosphorus compound has at least one
unsaturated group between adjacent carbon atoms and wherein
said unsaturation is present other than as an aromatic
compound, e.g., [figure] [caption], etc.
Subclass:
135
![[Patents]](../gifs/ps.gif)
This subclass is indented under subclass 134. Subject matter
wherein the unsaturation is in the form of a triple bond,
e.g., [figure] [caption], etc.
Subclass:
136
![[Patents]](../gifs/ps.gif)
Phosphate ester having three ester groups (e.g., DDVP,
etc.):
This subclass is indented under subclass 134. Subject matter
wherein the organo-phosphorus compound is a triester of
otho-phosphoric acid, e.g., as illustrated below, or sulfur
analog thereof, etc. [figure]
Subclass:
137
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to phosphorus:
This subclass is indented under subclass 75. Subject matter
wherein the organo-phosphorus compound has at least one
phosphorus to nitrogen bond.
SEE OR SEARCH THIS CLASS, SUBCLASS:
118 when another nitrogen atom other than nitro or nitroso
is present in the molecule which nitrogen is not directly
bonded to phosphorus.
Subclass:
138
![[Patents]](../gifs/ps.gif)
N-P-N or N-N-P containing:
This subclass is indented under subclass 137. Subject matter
wherein the organo-phosphorus compound has a N-P-N or N-N-P
chain therein.
Subclass:
139
![[Patents]](../gifs/ps.gif)
Phosphorus bonded directly to halogen:
This subclass is indented under subclass 75. Subject matter
wherein the organo-phosphorus compound has at least one
phosphorus to halogen bond.
Subclass:
140
![[Patents]](../gifs/ps.gif)
(C)(R)P=X(-XC) containing (i.e., phosphinate) (X is
chalcogen; R is C or H):
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound is an ester of
phosphinic acid, illustrated below, wherein R and R' are
organic radicals and X is chalcogen. [figure]
Subclass:
141
![[Patents]](../gifs/ps.gif)
(CX-) (C) P=X (XH) OR (CX-) (R) P=X (XC) containing (e.g.,
phosphonate, etc.):
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound is an ester of
phosphonic acid, illustrated below, wherein R is an organic
radical and X is chalcogen. [figure]
Subclass:
142
![[Patents]](../gifs/ps.gif)
(CX-)(C)P(C),(CX-)(RX-)P (C), (CX-) P (XH)(XH or (CX-)P(-XR)
containing (X is chalcogen: R is C or H) (e.g., phosphinite,
phosphonite, phosphite, etc.):
This subclass is indented under subclass 75. Subject matter
in which the organo-phosphorus compound is (a) an ester or
phosphinous acid (i.e., first illustration below), (b) an
ester of phosphonous acid, as in the second illustration,
below, or (c) an ester of phosphorus acid, as in the third
illustration, below, wherein R or R in any of the above
formulas is an organic radical and X is chalcogen. [figure]
Subclass:
143
![[Patents]](../gifs/ps.gif)
Ester or (HX) P=X (XH) (XH) (X is chalcogen) (e.g.,
phosphate, etc.):
This subclass is indented under subclass 775. Subject matter
in which the organo-phosphorus compound is an ester of an
acid whose structural formula is, as illustrated below,
wherein X is chalcogen. [figure]
Subclass:
144
![[Patents]](../gifs/ps.gif)
Triester:
This subclass is indented under subclass 143. Subject matter
which the organo-phosphorus compound is a triester of
orthophosphoric acid, illustrated below, wherein X is
chalcogen. [figure]
Subclass:
145
![[Patents]](../gifs/ps.gif)
Three benzene rings bonded directly to chalcogen:
This subclass is indented under subclass 144. Subject matter
wherein the organo-phosphorus compound has three benzene
rings attached directly to chalcogens which are bonded
directly to a single phosphorus atom.
SEE OR SEARCH THIS CLASS, SUBCLASS:
146 for the compound, illustrated below, which is considered
to have only two benzene rings attached to chalcogens which
are bonded directly to phosphorus. [figure]
Subclass:
146
![[Patents]](../gifs/ps.gif)
Two benzene rings bonded directly to chalcogen:
This subclass is indented under subclass 144. Subject matter
wherein the organo-phosphorus compound has at least two
benzene rings attached directly to chalcogens which are
bonded to a single phosphorus atom.
SEE OR SEARCH THIS CLASS, SUBCLASS:
147 for the compound, illustrated below, which is considered
to have only one benzene ring bonded to chalcogen which is
bonded directly to phosphorus. [figure]
Subclass:
147
![[Patents]](../gifs/ps.gif)
One benzene ring bonded directly to chalcogen:
This subclass is indented under subclass 144. Subject matter
wherein the organo-phosphorus compound has one benzene ring
attached directly to a chalcogen which is directly bonded to
a phosphorus atom.
Subclass:
148
![[Patents]](../gifs/ps.gif)
Diester:
This subclass is indented under subclass 143. Subject matter
wherein the organo-phosphorus compound has the formula,
illustrated below, wherein R is an organic radical and X is
chalcogen. [figure]
Subclass:
149
![[Patents]](../gifs/ps.gif)
Azoxy DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the active DOAI contains the azoxy group, i.e.,
-N(O)=N-, wherein each nitrogen is bonded directly to
carbon.
(1) Note. Subject matter containing a -N=N- groups as part
of a ring is classified in subclass 183.
(2) Note. The azoxy group may also be represented as
shown below. [figure]
Subclass:
150
![[Patents]](../gifs/ps.gif)
Acyclic nitrogen double bonded to acyclic nitrogen, acyclic
nitrogen triple bonded to acyclic nitrogen or azide DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the active DOAI contains an acyclic nitrogen which is
double or triple bonded to another acyclic nitrogen, i.e.,
-N=N- or --ANION, as illustrated below, (diazonium) or azide,
etc. [figure] [caption]e.g., [figure]
SEE OR SEARCH THIS CLASS, SUBCLASS:
183 for a -N=N- group as part of a hetero ring.
Subclass:
151
![[Patents]](../gifs/ps.gif)
Acyclic C-N=N-N containing:
This subclass is indented under subclass 150. Subject matter
wherein the active ingredient contains the C-N=N-N grouping
e.g., [figure] [caption], etc.
(1) Note. Subject matter which contains -N=N-N- as part of
a ring is classified in subclass 183.
Subclass:
152
![[Patents]](../gifs/ps.gif)
3,10-dihydroxy-2-naphthacene carboxamide or derivative (e.g.,
tetracycline, etc.) DOAI:
This subclass is indented under subclass 1. Subject matter
which contains an active DOAI which has the 3,10
dihydroxy-2-naphthacenecarboxamide nucleus, e.g.,
(tetracycline), [figure] [caption], etc.
Subclass:
153
![[Patents]](../gifs/ps.gif)
With stabilizer or preservative:
This subclass is indented under subclass 152. Subject matter
wherein an additional agent is present which is disclosedas a
stabilizer or preservative for the
3,10-dihydroxy-2-naphthacenecarboxamide compound.
Subclass:
154
![[Patents]](../gifs/ps.gif)
With an additional active ingredient (excludes reaction
product or complex):
This subclass is indented under subclass 152. Subject matter
which contain a compound and an additional active
ingredient.
(1) Note. Reaction products, complexes and mixtures
comprising two or moreactive compounds which havethe
3,10-dihydroxy-2-naphthacenecarboxamide nucleus are included
herein.
Subclass:
155
![[Patents]](../gifs/ps.gif)
Para-N-benzene - sulfoxy-N containing DOAI, and said benzene
ring is not part of a polycyclo ring system:
This subclass is indented under subclass 1. Subject matter
which contains a DOAI which has the structural group, as
illustrated below and no ring of any type is fused onto the
benzene nucleus, e.g., sulfanilamide,
p-nitrobenzenesulfonylhydrazone, etc. [figure] [caption]Or
[figure]
Subclass:
156
![[Patents]](../gifs/ps.gif)
Hetero ring containing:
This subclass is indented under subclass 155. Subject matter
wherein the active ingredient having at least one group,
shown in the first illustration below, also contains a
heterocyclic group, e.g., sulfapyridine, shown in the second
illustration, below. [figure] [figure] [caption], etc.
Subclass:
157
![[Patents]](../gifs/ps.gif)
The hetero ring is six-membered and includes at least two
nitrogens and no other hetero atoms:
This subclass is indented under subclass 156. Subject matter
wherein the heterocyclic ring has six members and includes at
least two nitrogen and no other hetero atoms.
Subclass:
158
![[Patents]](../gifs/ps.gif)
The hetero ring is five-membered:
This subclass is indented under subclass 156. Subject matter
wherein the heterocyclic group has five members, e.g.,
sulfamoxole, [figure] [caption], etc.
Subclass:
159
![[Patents]](../gifs/ps.gif)
Ortho-hydroxybenzoic acid (i.e., salicylic acid) or
derivative DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the organic active ingredient contains salicylic acid
as shown in the first illustration, below, or a derivative
thereof which contains the moiety, as shown in the second
illustration, below, said derivative being other than another
ring fused onto the benzoic acid moiety or the
ortho-hydroxybenzoic acid salts of a bioactive organic
compound. [figure] [figure]
(1) Note. This subclass includes ring structures derived
from the carboxy and hydroxyl moieties.
(2) Note. The ortho-hydroxybenzoic acid salts of organic
compounds are excluded herefrom and are classified in the
appropriate subclasses below based on the bioactive
compound.
Subclass:
160
![[Patents]](../gifs/ps.gif)
With additional ortho-hydroxybenzoic acid compound:
This subclass is indented under subclass 159. Subject matter
wherein two or more bioactive organic compounds each having
the moiety are present. [figure]
(1) Note. The combination of salicylic acid and a salt
thereof is in this subclass.
Subclass:
161
![[Patents]](../gifs/ps.gif)
With heterocyclic compound:
This subclass is indented under subclass 159. Subject matter
wherein a heterocyclic compound is present in addition to the
salicylic acid compound.
Subclass:
162
![[Patents]](../gifs/ps.gif)
With organic nitrogen containing compound:
This subclass is indented under subclass 159. Subject matter
wherein an organic nitrogen compound is present in addition
to the salicylic acid compound.
Subclass:
163
![[Patents]](../gifs/ps.gif)
With carboxylic acid, ester or metal salt thereof:
This subclass is indented under subclass 159. Subject matter
wherein a carboxylic acid, ester or metal salt thereof is
present in addition to the salicylic acid compound.
Subclass:
164
![[Patents]](../gifs/ps.gif)
With organic oxygen containing compound:
This subclass is indented under subclass 159. Subject matter
wherein an organic oxygen compound is present in addition to
the salicylic acid compound.
Subclass:
165
![[Patents]](../gifs/ps.gif)
Aspirin, per se, (i.e., 2-(acetyloxy) benzoic acid):
This subclass is indented under subclass 159. Subject matter
wherein the organic active ingredient is 2-(acetyloxy benzoic
acid): [figure]
Subclass:
166
![[Patents]](../gifs/ps.gif)
Nitrogen containing (e.g., anilides, etc.):
This subclass is indented under subclass 159. Subject matter
wherein the salicylic acid compound contains nitrogen, e.g.,
anilides, etc.
Subclass:
167
![[Patents]](../gifs/ps.gif)
9,10-seco cyclopentanohydrophenanthrene ring system (e.g.,
vitamin D, etc.) DOAI:
Subject matter under subclass wherein the organic active
ingredient contains a 9,
10-seco-cyclopentanohydrophenanthrene nucleus, i.e.,
[figure]
(1) Note. Such terms as "activated ergosterol", vitamin D,
ergocalciferol, cholecalciferol and antirachitic vitamin will
suffice for classification of an active ingredient in this
subclass.
Subclass:
168
![[Patents]](../gifs/ps.gif)
With a vitamin type active ingredient:
This subclass is indented under subclass 167. Subject matter
wherein an additional vitamin type active compound is present
in addition to the 9, 10 seco-cyclopentanohydrophenanthrene
compound, e.g., vitamin A, etc.
Subclass:
169
![[Patents]](../gifs/ps.gif)
Cyclopentanohydrophenanthrene ring system DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the organic active ingredient has the
cyclopentanohydrophenanthrene nucleus, illustrated below, and
may contain double bond between its members. [figure]
(1) Note. Included herein is lanolin as the active
ingredient.
Subclass:
170
![[Patents]](../gifs/ps.gif)
Plural compounds containing cyclopentanohydrophenanthrene
ring systems:
This subclass is indented under subclass 169. Subject matter
wherein two or more bioactive compounds are present each of
which contains the cyclopentanohydrophenanthrene ring
system.
Subclass:
171
![[Patents]](../gifs/ps.gif)
With additional active ingredient:
This subclass is indented under subclass 169. Subject matter
wherein an organic bioactive ingredient is present in
addition to the cyclopentanohydrophenanthrene ring containing
compound.
Subclass:
172
![[Patents]](../gifs/ps.gif)
Hetero ring containing:
This subclass is indented under subclass 169. Subject matter
wherein the cyclopentanohydrophenanthrene ring containing
compound contains a heterocyclic ring. Included herein are:
[figure] [caption]and [figure] [caption], etc.
Subclass:
173
![[Patents]](../gifs/ps.gif)
Spiro ring system:
This subclass is indented under subclass 172. Subject matter
wherein a spiro ring is attached directly or indirectly to a
carbon of the cyclopentanohydrophenanthrene nucleus.
Subclass:
174
![[Patents]](../gifs/ps.gif)
-O-C-O- is part of a hetero ring (e.g., acetonide, etc.):
This subclass is indented under subclass 172. Subject matter
wherein an -O-C-O- containing hetero ring is attached or
fused to the cyclopentanohydrophenanthrene nucleus.
Subclass:
175
![[Patents]](../gifs/ps.gif)
-C(=O)-O- is part of a hetero ring (e.g., lactone, etc.):
This subclass is indented under subclass 172. Subject matter
wherein -O-C(=O)- is part of the hetero ring attached or
fused to the cyclopentanohydrophenanthrene nucleus.
Subclass:
176
![[Patents]](../gifs/ps.gif)
Nitrogen containing hetero ring:
This subclass is indented under subclass 172. Subject matter
wherein the hetero ring contains at least one nitrogen atom.
Subclass:
177
![[Patents]](../gifs/ps.gif)
Oxygen double bonded to a ring carbon or the
cyclopentanohydrophenanthrene ring system:
This subclass is indented under subclass 169. Subject matter
wherein a nuclear carbon of the cyclopentanohydrophenanthrene
nucleus is bonded to an oxygen atom through a double bond
(C=O).
Subclass:
178
![[Patents]](../gifs/ps.gif)
Oxygen single bonded to a ring carbon of the
cyclopentanohydrophenanthrene ring system:
This subclass is indented under subclass 177. Subject matter
wherein one nuclear carbon of the
cyclopentanohydrophenanthrene nucleus is bonded to an oxygen
through a double bond and wherein another nuclear carbon atom
of said cyclopentanohydrophenanthrene is bonded to at least
one other oxygen through a single bond as, e.g., ether,
hydroxy or alcoholate, etc.
Subclass:
179
![[Patents]](../gifs/ps.gif)
Modified C-ring (except methyl in 13-position) (e.g., double
bond containing substituted, etc.):
This subclass is indented under subclass 178. Subject matter
wherein the C-ring of the cyclopentanohydrophenanthrene ring
system contains a double bond or is substituted, other than
-CH[subscrpt]3[end subscrpt] in 13-position, i.e.,
18-methyl.
(1) Note. For the purpose of this classification, the
C-ring is defined as including positions 8, 9, 11, 12, 13,
and 14.
(2) Note. See subclass 169 for the numbering system of a
cyclopentanohydrophenanthrene nucleus.
(3) Note. This subclass contains for example: [figure]
[figure] [caption], etc.
Subclass:
180
![[Patents]](../gifs/ps.gif)
9-position substituted:
This subclass is indented under subclass 179. Subject matter
wherein the cyclopentanohydrophenanthrene is substituted.
Subclass:
181
![[Patents]](../gifs/ps.gif)
21-position substituted:
This subclass is indented under subclass 178. Subject matter
wherein the carbon in the 21 position is directly bonded to
an atom other than carbon or hydrogen.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
182
![[Patents]](../gifs/ps.gif)
Oxygen singly bonded to a ring carbon of the
cyclopentanohydrophenanthrene ring system:
This subclass is indented under subclass 169. Subject matter
wherein a nuclear carbon of the cyclopentanohydrophenanthrene
nucleus is bonded to an oxygen through a single bond [figure]
[caption]Cholestrol.
Subclass:
183
![[Patents]](../gifs/ps.gif)
Heterocyclic carbon compounds containing a hetero ring having
chalcogen (i.e., O, S, Se, or Te) or nitrogen as the only
ring hetero atoms DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing a ring composed of
carbon and at least one element from the group consisting of
nitrogen, sulfur, selenium, tellurium and oxygen as DOAI.
(1) Note. Excluded herefrom are those carbon compounds
wherein the only heterocyclic nucleus present is produced by
salt formation between amino and acid groups, e.g., betaines,
which are placed with the corresponding open chain compounds,
particularly subclass 556.
Subclass:
184
![[Patents]](../gifs/ps.gif)
Heavy metal-containing (including salts):
This subclass is indented under subclass 183. Subject matter
in which the heterocyclic compound includes a heavy metal.
(1) Note. This subclass includes salts.
Subclass:
185
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 184. Subject matter
wherein the heterocyclic compound which includes a heavy
metal is a part of a fused ring or bridged ring system.
Subclass:
186
![[Patents]](../gifs/ps.gif)
Bicyclo ring system:
This subclass is indented under subclass 185. Subject matter
wherein the polycyclo system comprises only two rings.
Subclass:
187
![[Patents]](../gifs/ps.gif)
Quinolines or isoquinolines (including hydrogenated):
This subclass is indented under subclass 186. Subject matter
in which the bicyclo forms a quinoline or isoquinoline ring
or hydrogenated forms thereof, e.g., [figure] [figure]
[caption], etc.
Subclass:
188
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered consisting of one nitrogen and
five carbons:
This subclass is indented under subclass 184. Subject matter
wherein the heterocyclic ring consists of five carbons and
one nitrogen.
Subclass:
189
![[Patents]](../gifs/ps.gif)
Tin:
This subclass is indented under subclass 184. Subject matter
wherein the heavy metal is tin.
Subclass:
190
![[Patents]](../gifs/ps.gif)
Mercury:
This subclass is indented under subclass 184. Subject matter
wherein the heavy metal is mercury.
Subclass:
191
![[Patents]](../gifs/ps.gif)
Aluminum (including salts):
This subclass is indented under subclass 184. Subject matter
in which the heterocyclic compound includes aluminum.
(1) Note. This subclass includes salts.
Subclass:
192
![[Patents]](../gifs/ps.gif)
1-thia-4-aza-bicyclo (3.2.0.) heptane ring containing
(including dehydrogenated) e.g., penicillins, etc.):
This subclass is indented under subclass 183. Subject matter
wherein the heterocyclic compound contains a 1-thia- 4-
aza-bicyclo (3.2.0) heptane ring system having the following
structure, and may contain a double bond between ring
members, e.g., penicillins, etc. [figure]
(1) Note. The Ring Index uses a different system for
numbering the ring members. However, in the indents
hereunder which refer to positions, the numbers shown in the
definition are employed.
(2) Note. Patents reciting broadly "penicillins,"
"penicillin type," or "penicillin drugs" are placed herein.
SEE OR SEARCH CLASS:
435, Chemistry: Molecular Biology and Microbiology, subclass
43 for processes of producing penicillin by microbial
fermentation.
540, Organic Compounds, 304 for a penicillin compound, per
se.
Subclass:
193
![[Patents]](../gifs/ps.gif)
Spiro or addition polycyclo ring system:
This subclass is indented under subclass 192. Subject matter
which contains a spiro ring system, or an additional
polycyclo ring system.
Subclass:
194
![[Patents]](../gifs/ps.gif)
6,6-di-substituted:
This subclass is indented under subclass 192. Subject matter
wherein the bicyclo heptane ring system contains two
substituents other than hydrogen in 6-position.
Subclass:
195
![[Patents]](../gifs/ps.gif)
3-position substituent contains -COOC- group:
This subclass is indented under subclass 192. Subject matter
wherein a substituent in 3-position of the bicyclo heptane
ring system contains a -COOC- group, e.g., ester, etc.
Subclass:
196
![[Patents]](../gifs/ps.gif)
6-position substituent contains hetero ring:
This subclass is indented under subclass 192. Subject matter
wherein a substituent in 6-position of the bicyclo heptane
ring system contains a hetero ring.
Subclass:
197
![[Patents]](../gifs/ps.gif)
6-position substituent contains carbocyclic ring:
This subclass is indented under subclass 192. Subject matter
wherein a substituent in 6-position of the bicyclo heptane
ring system contains a carbocyclic ring.
Subclass:
198
![[Patents]](../gifs/ps.gif)
Ampicillin, per se, or salt thereof:
This subclass is indented under subclass 197. Subject matter
wherein the heterocyclic compound is ampicillin having the
following structure, illustrated below, or salt thereof.
[figure]
Subclass:
199
![[Patents]](../gifs/ps.gif)
Penicillin G, per se, or salt thereof (e.g., procaine
penicillin G, etc.):
This subclass is indented under subclass 197. Subject matter
wherein the heterocyclic compound is penicillin G or salt
thereof, e.g., [figure] [caption], etc.
Subclass:
200
![[Patents]](../gifs/ps.gif)
1-thia-5-aza-bicyclo (4.2.0) octane ring containing
(including dehydrogenated) (e.g., cephalosporins, etc.):
This subclass is indented under subclass 183. Subject matter
wherein the heterocyclic compound contains a
1-thia-5-aza-bicyclo (4.2.0.) octane ring system having the
following structure, illustrated below, and may contain
double bond between ring members, e.g., cephalosporin, etc.
[figure]
(1) Note. The Ring Index uses a different system for
numbering the ring members. However, in the indents
hereunder which refer to positions, the numbers shown in the
definition are employed.
Subclass:
201
![[Patents]](../gifs/ps.gif)
7,7-di-substituted:
This subclass is indented under subclass 200. Subject matter
wherein the bicyclo octane ring system contains two
substituents other than hydrogen in 7-position.
Subclass:
202
![[Patents]](../gifs/ps.gif)
Addition hetero ring:
This subclass is indented under subclass 200. Subject matter
wherein the bicyclo octane ring system contains an additional
hetero ring.
Subclass:
203
![[Patents]](../gifs/ps.gif)
3-Position substituent contains pyridine ring:
This subclass is indented under subclass 202. Subject matter
wherein a substituent in 3-position of the bicyclo octane
ring system contains a pyridine ring.
Subclass:
204
![[Patents]](../gifs/ps.gif)
3-position substituent contains sulfur:
This subclass is indented under subclass 202. Subject matter
wherein a substituent in 3-position of the bicyclo octane
ring system contains sulfur, e.g., [figure] [caption]etc.
Subclass:
205
![[Patents]](../gifs/ps.gif)
The additional hetero ring is part of a polycyclo ring
system:
This subclass is indented under subclass 204. Subject matter
wherein the additional hetero ring is part of a polycyclo
ring system.
Subclass:
206
![[Patents]](../gifs/ps.gif)
7-position substituent contains hetero ring:
This subclass is indented under subclass 204. Subject matter
wherein a substituent in 7-position contains a hetero ring.
Subclass:
207
![[Patents]](../gifs/ps.gif)
Alkyl, hydroxyalkyl, alkoxyalkyl, or alkanoloxyalkyl bonded
directly to 3-position:
This subclass is indented under subclass 202. Subject matter
wherein alkyl, alkyl-OH, alkyl-O-alkyl, or
alkyl-C(=O)-O-alkyl is bonded directly to 3-position of the
bicyclo octane ring system.
Subclass:
208
![[Patents]](../gifs/ps.gif)
Sulfur containing substituent:
This subclass is indented under subclass 200. Subject matter
wherein the bicyclo octane ring system contains sulfur.
Subclass:
209
![[Patents]](../gifs/ps.gif)
Alkyl, hydroxyalkyl, alkoxyalkyl, or alkanoloxyalkyl bonded
directly to 3-position:
This subclass is indented under subclass 200. Subject matter
wherein alkyl, alkyl-OH, alkyl-O-alkyl, alkyl-C(=O)-O-alkyl
is bonded directly to 3-position of the bicyclo octane ring
system.
Subclass:
210.01
![[Patents]](../gifs/ps.gif)
Hetero ring is four-membered and includes at least one ring
nitrogen:
This subclass is indented under subclass 183. Subject
matter which contains a heterocyclic ring consisting of four
atoms, at least one of which is nitrogen.
(1) Note. The heterocyclic ring may include other hetero
atoms of the group set forth in the definition of subclass
183 and the relative positions of the hetero atoms
may vary.
SEE OR SEARCH CLASS:
540, Chemistry, Carbon Compounds, Part of the Class 532-570
Series, subclasses 200-364 for a compound which includes a
four-membered lactam ring.
548, Carbon Compounds, Part of the 532-570 Series, subclasses
950-953, for a compound which includes a non-lactam
four-membered hetero ring containing nitrogen.
Subclass:
210.02
![[Patents]](../gifs/ps.gif)
Chalcogen double bonded directly to a ring carbon of the
four-membered hetero ring which is adjacent to the ring
nitrogen:
This subclass is indented under subclass 210.01. Subject
matter wherein chalcogen (i.e., oxygen, sulfur, selenium
or tellurium) is double bonded
directly to one of the carbons of the four-membered hetero
ring which is adjacent to the ring nitrogen.
Subclass:
210.03
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the four-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 210.02. Subject
matter wherein the four-membered hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
210.04
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the four-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 210.03. Subject
matter in which the polycyclo ring system consists
of exactly two rings.
Subclass:
210.05
![[Patents]](../gifs/ps.gif)
Plural ring hetero atoms in the bicyclo ring system:
This subclass is indented under subclass 210.04. Subject
matter wherein the bicyclo ring system contains
an additional hetero atom (i.e. nitrogen,
oxygen, sulfur, selenium, or tellurium).
(1) Note. An example of an active ingredient provided for
herein is, [figure]
SEE OR SEARCH THIS CLASS, SUBCLASS:
192 for when the additional hetero atom is sulfur, and the
bicyclo ring system is 1-thia-4-aza-bicyclo (3.2.0) heptane.
200 for when the hetero atom is sulfur, and the bicyclo ring
system is 1-thia-5-aza- bicyclo (4.2.0) octane.
Subclass:
210.06
![[Patents]](../gifs/ps.gif)
Ring oxygen in the bicyclo ring system:
This subclass is indented under subclass 210.05. Subject
matter wherein the additional hetero atom is oxygen
Subclass:
210.07
![[Patents]](../gifs/ps.gif)
The other cyclo of the bicyclo ring system is six-membered:
This subclass is indented under subclass 210.06. Subject
matter wherein a six membered ring is the other cyclo
of the bicyclo ring system.
Subclass:
210.08
![[Patents]](../gifs/ps.gif)
1-Oxa-5-aza-bicyclo(4.2.0)octanes ( including unsaturated ):
This subclass is indented under subclass 210.07. Subject
matter in which the bicyclo ring system has the
following basic structure, wherein X is chalcogen (i.e.,
oxygen, sulfur, selenium, or tellurium) and the
structure may contain double bonds between ring members:
[figure]
Subclass:
210.09
![[Patents]](../gifs/ps.gif)
The other cyclo of the bicyclo ring system is five-membered:
This subclass is indented under subclass 210.04. Subject
matter wherein the other cyclo in the bicyclo
ring system consists of five
members.
Subclass:
210.10
![[Patents]](../gifs/ps.gif)
Sulfur bonded directly to the five-membered cyclo of the
bicyclo ring system (e.g., thienamycin, etc.):
This subclass is indented under subclass 210.09. Subject
matter wherein the five-membered cyclo of of the bicyclo ring
system is bonded directly to sulfur.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
210.11
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly to the sulfur by
nonionic bonding:
This subclass is indented under subclass 210.10. Subject
matter wherein the sulfur is attached directly by nonionic
bonding to an additional hetero ring (i.e. a ring consisting
of carbon and at least one ring member selected from nitrogen
and chalcogen).
Subclass:
210.12
![[Patents]](../gifs/ps.gif)
The additional hetero ring contains ring nitrogen:
This subclass is indented under subclass 210.11. Subject
matter wherein nitrogen is a ring member of the additional
hetero ring.
Subclass:
210.13
![[Patents]](../gifs/ps.gif)
Having C(=X)-, wherein X is chalcogen, bonded directly to
the additional hetero ring:
This subclass is indented under subclass 210.12. Subject
matter wherein the additional hetero ring is bonded directly
to a C(=X)- group, wherein X is chalcogen (i.e. oxygen,
sulfur, selenium or tellurium).
Subclass:
210.14
![[Patents]](../gifs/ps.gif)
Polycyclo ring system bonded to the five-membered cyclo of
the bicyclo ring system:
This subclass is indented under subclass 210.09. Subject
matter wherein the five-membered cyclo of the bicyclo ring
system is bonded directly to a polycyclo ring system
(1) Note. The polycyclo ring system may include a nitrogen-
or chalcogen-containing hetero ring.
Subclass:
210.15
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to the ring nitrogen of the
four-membered ring by nonionic
bonding
This subclass is indented under subclass 210.02. Subject
matter wherein a chalcogen (i.e. oxygen, sulfur, selenium, or
tellurium) is bonded directly to the ring nitrogen of the
four-membered ring by nonionic bonding.
Subclass:
210.16
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the four- membered hetero ring
as one of the cyclos:
This subclass is indented under subclass 210.01. Subject
matter wherein the four-membered hetero ring is one of
the cyclos in a polycyclo ring system.
Subclass:
210.17
![[Patents]](../gifs/ps.gif)
Having -C(=X)-, wherein X is chalcogen, bonded directly to
the four membered
hetero ring:
This subclass is indented under subclass 210.01. Subject
matter wherein a -C(=X)- group, wherein X is chalcogen
(i.e. oxygen, sulfur, selenium or tellurium), is
attached directly to the four membered
hetero ring.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
210.18
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
four-membered heteroby nonionic bonding:
This subclass is indented under subclass 210.17. Subject
matter wherein the four-membered hetero ring is attached
directly or indirectly by nonionic bonding
to an additional hetero ring.
Subclass:
210.19
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
four-membered hetero ring by nonionic
bonding:
This subclass is indented under subclass 210.01. Subject
matter wherein the four-membered hetero ring is attached
directly or indirectly by nonionic bonding.to an additional
hetero ring.
Subclass:
210.20
![[Patents]](../gifs/ps.gif)
The additional hetero ring contains ring nitrogen:
This subclass is indented under subclass 210.19. Subject
matter wherein the additional hetero ring contains at least
one nitrogen as a ring hetero atom.
Subclass:
210.21
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional hetero ring as
one of the cyclos:
This subclass is indented under subclass 210.20. Subject
matter wherein the additional hetero ring is part of a
polycyclo ring system.
Subclass:
211.01
![[Patents]](../gifs/ps.gif)
Hetero ring contains seven members including nitrogen,
carbon, and chalcogen:
This subclass is indented under subclass 183. Subject
matter which contains a hetero ring having exactly seven
members consisting of carbon, nitrogen and
chalcogen (i.e., oxygen, sulfur, selenium, or
tellurium as its only ring members)..
SEE OR SEARCH CLASS:
540, Chemistry, Carbon Compounds, Part of the 532-570 Series,
subclasses 488-491 for seven-membered lactams containing a
chalcogen ring atom in the
lactam ring, subclasses 544 through 552 for non-lactam
seven-membered hetero ring compounds which include nitrogen
and chalcogen as ring atoms of the seven-membered hereto
ring.
Subclass:
211.02
![[Patents]](../gifs/ps.gif)
Monocyclic cyclopentyl ring bonded directly to the
seven-membered hetero ring (e.g.,
prostaglandins, etc.):
This subclass is indented under subclass 211.01. Subject
matter wherein the seven-membered hetero ring is
bonded directly to a monocyclic cyclopentyl ring
Subclass:
211.03
![[Patents]](../gifs/ps.gif)
Chalcogen double bonded directly to a ring carbon which is
adjacent to the ring nitrogen:
This subclass is indented under subclass 211.01. Subject
matter wherein a chalcogen (i. oxygen, sulfur, selenium, or
tellurium) is double bonded directly to a ring carbon which
is adjacent to the ring nitrogen of the seven-membered hetero
ring.
Subclass:
211.04
![[Patents]](../gifs/ps.gif)
Polycyclo ring system which contains the seven-membered
hetero ring as of the cyclos:
This subclass is indented under subclass 211.03. Subject
matter wherein the seven-membered hetero ring is one of
the cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
211.05
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the seven-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 211.04. Subject
matter wherein the polycyclo ring system
consists of exactly two rings.
Subclass:
211.06
![[Patents]](../gifs/ps.gif)
Ring chalcogen and ring nitrogen are in the 1,5 positions of
the seven-membered hetero ring
This subclass is indented under subclass 211.05. Subject
matter wherein chalcogen and nitrogen are in the 1- and
5-positions, respectively, of the seven-membered hetero
ring.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
211.07
![[Patents]](../gifs/ps.gif)
Nitrogen attached directly or indirectly to the ring nitrogen
of the seven- membered hetero ring by acyclc
nonionic bonding ( e.g. Diltiazem, etc.):
This subclass is indented under subclass 211.06. Subject
matter wherein the ring nitrogen of the seven-membered hetero
ring is attached directly or indirectly to nitrogen by
nonionic bonding.
(1) Note. Diltiazem is 2-(p-methoxyphenyl)-3-acetoxy-
5-N,N-dimethylaminoethyl-1,5-benzothiazepin-4-one, of the
following formula: [figure]
Subclass:
211.08
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens in the seven-membered hetero ring:
This subclass is indented under subclass 211.01. Subject
matter wherein the seven-membered hetero ring contains at
least two ring nitrogens.
SEE OR SEARCH CLASS:
540, Chemistry, Carbon Compounds, Part of the 532-570 Series,
subclass 545, for compounds which contain chalcogen and at
least two ring nitrogens in
a seven-membered hetero ring.
Subclass:
211.09
![[Patents]](../gifs/ps.gif)
Polycyclo ring system which contains the seven-membered
hetero ring as one of the cyclos:
This subclass is indented under subclass 211.01. Subject
matter wherein the seven-membered hetero ring is one of the
cyclos of a polycyclo ring system.
Subclass:
211.10
![[Patents]](../gifs/ps.gif)
Three ring hetero atoms in the polycyclo ring system:
This subclass is indented under subclass 211.09. Subject
matter wherein the polycyclo ring system contains at
least three ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
211.11
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the seven-membered hetero ring as
one of the cyclos:
Subject matter under 211.09 wherein the polycyclo ring
system consists of exactly three rings.
Subclass:
211.12
![[Patents]](../gifs/ps.gif)
Ring nitrogen is shared by plural cyclos of the tricyclo ring
system:
This subclass is indented under subclass 211.11. Subject
matter wherein plural cyclos of the tricyclo ring system
share ring nitrogen.
Subclass:
211.13
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to ring carbon of the seven-membered
hetero ring:
This subclass is indented under subclass 211.11. Subject
matter wherein a ring carbon of the seven-membered hetero
ring is bonded directly to nitrogen.
(1) Note. Examples of active ingredients provided for herein
are, [figure]
Subclass:
211.14
![[Patents]](../gifs/ps.gif)
Having -C(=X)-, wherein X is chalcogen, bonded directly to
the seven-membered hetero ring :
This subclass is indented under subclass 211.11. Subject
matter wherein the seven-membered hetero ring is bonded to a
C(=X)- group, wherein X is chalcogen (i.e. oxygen, sulfur,
selenium or tellurium).
Subclass:
211.15
![[Patents]](../gifs/ps.gif)
Additional nitrogen containing hetero ring attached directly
or indirectly to the seven-membered hetero ring by nonionic
bonding:
This subclass is indented under subclass 211.01. Subject
matter wherein the seven-membered hetero ring is attached
directly or indirectly by nonionic bonding to an additional
nitrogen-containing hetero ring.
Subclass:
212.01
![[Patents]](../gifs/ps.gif)
Hetero ring is seven-membered consisting of one nitrogen and
six carbons:
This subclass is indented under subclass 183. Subject
matter wherein the hetero ring has seven members and consists
of one ring nitrogen and six carbon atoms.
SEE OR SEARCH CLASS:
540, Chemistry, Carbon Compounds, Part of the 530-570 Series,
subclasses 519-540 for a lactam ring compound wherein the
ring consists of nitrogen and six carbon atoms, and
subclasses 576-612 for a non-lactam compound having a hetero
ring consisting one nitrogen and six carbons.
Subclass:
212.02
![[Patents]](../gifs/ps.gif)
Spiro:
Subject matter under 212.01 wherein a ring is spiro fused
directly or indirectly to the seven-membered hetero ring.
(1) Note. An example of an active ingredient provided
herein is: [figure]
Subclass:
212.03
![[Patents]](../gifs/ps.gif)
Chalcogen double bonded directly to a ring carbon of the
seven-membered hetero ring which is adjacent to the ring
nitrogen:
This subclass is indented under subclass 212.01. Subject
matter wherein chalcogen (i.e. oxygen, sulfur, selenium, or
tellurium) is double bonded directly to a ring carbon of the
seven-membered hetero ring which is adjacent to the ring
nitrogen.
Subclass:
212.04
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the seven-membered hetero ring
as one of the cyclos:
This subclass is indented under subclass 212.03. Subject
matter wherein the seven-membered hetero ring is one of the
cyclos of a polycyclo ring system.
Subclass:
212.05
![[Patents]](../gifs/ps.gif)
Plural cyclos of the polycyclo ring system share ring
nitrogen of the seven-membered hetero ring:
This subclass is indented under subclass 212.04. Subject
matter wherein the ring nitrogen of the seven membered hetero
ring is shared by plural cyclos of the polycyclo ring
system.
Subclass:
212.07
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the seven-membered hetero ring as
one of the cyclos :
This subclass is indented under subclass 212.04. Subject
matter wherein the polycyclo ring system consists
of exactly two rings.
Subclass:
212.08
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly by
nonionic bonding to the seven-membered hetero ring:
This subclass is indented under subclass 212.03. Subject
matter wherein the seven-membered hetero ring is attached
directly or indirectly to an additional hetero ring by
nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
213.01
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the seven-membered hetero ring
as one of the cyclos:
This subclass is indented under subclass 212.01. Subject
matter wherein the seven-membered hetero ring is one of the
cyclos of a polycyclo ring.
Subclass:
214.01
![[Patents]](../gifs/ps.gif)
Ring nitrogen of the seven-membered hetero ring is shared by
an additional cyclo of the polycyclo ring
system:
This subclass is indented under subclass 213.01. Subject
matter wherein the ring nitrogen of the seven-membered hetero
ring is also a member of an additional cyclo of the polycyclo
ring system.
Subclass:
214.02
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens in the polycyclo ring system
This subclass is indented under subclass 214.01. Subject
matter wherein the polycyclo ring system has two or more ring
nitrogens.
Subclass:
214.03
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring members (i.e.
bridged):
This subclass is indented under subclass 214.01. Subject
matter wherein two cyclos of the polycyclo ring system
share at least three ring members.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
215
![[Patents]](../gifs/ps.gif)
Additional hetero atom in the polycyclo ring system:
This subclass is indented under subclass 213.01. Subject
matter wherein the polycyclo ring system contains at least
one ring hetero atom in addition to the ring nitrogen of the
seven-membered hetero ring.
Subclass:
216
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring carbons (i.e.,
bridged):
This subclass is indented under subclass 213.01. Subject
matter wherein two cyclos of the polycyclo ring system share
at least three ring carbons.
(1) Note. An example of a compound provided for herein is:
[figure] [caption] etc.
Subclass:
217
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the seven-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 213.01. Subject
matter wherein the polycyclo ring system consists of exactly
three rings.
Subclass:
217.01
![[Patents]](../gifs/ps.gif)
3-Benzazepines (including hydrogenated):
This subclass is indented under subclass 213.01. Subject
matter wherein the polycyclo ring system has the
following structure which may contain double bonds between
its members: [figure]
Subclass:
217.02
![[Patents]](../gifs/ps.gif)
Benzene ring bonded directly to ring carbon of the
seven-membered hetero ring:
Subject matter under 217.01 wherein a ring carbon of the
seven-membered hetero ring is bonded directly
to an optionally substituted benzene ring.
Subclass:
217.03
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
seven-membered hetero ring by nonionic bonding:
This subclass is indented under subclass 212.01. Subject
matter wherein the seven-membered hetero ring is attached
directly or indirectly by nonionic bonding.to an additional
hetero ring
Subclass:
217.04
![[Patents]](../gifs/ps.gif)
The additional hetero ring is six-membered and contains
nitrogen:
This subclass is indented under subclass 217.03. Subject
matter wherein nitrogen is a ring member of the additional
hetero ring, which is six-membered.
Subclass:
217.05
![[Patents]](../gifs/ps.gif)
Plural ring hetero atoms in the additional hetero ring:
Subject matter under 217.04 wherein the additional hetero
ring has at least two ring hetero atoms
Subclass:
217.06
![[Patents]](../gifs/ps.gif)
The additional hetero ring is a 1,3 diazine (including
hydrogenated):
This subclass is indented under subclass 217.05. Subject
matter wherein the additional hetero ring has the following
structure [figure]
(1) Note. An example of active ingredients provided for
herein is, [figure]
Subclass:
217.07
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional six-membered
hetero ring as one of the cyclos:
This subclass is indented under subclass 217.04. Subject
matter wherein the additional six-membered hetero ring
is one of the cyclos of a polycyclo ring system.
Subclass:
217.08
![[Patents]](../gifs/ps.gif)
The additional hetero ring is five-membered and contains
nitrogen:
This subclass is indented under subclass 217.03. Subject
matter wherein nitrogen is a ring member of the additional
hetero ring, which is five-membered.
Subclass:
217.09
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the additional hetero ring:
This subclass is indented under subclass 217.08. Subject
matter wherein the additional hetero ring contains at least
two ring hetero atoms, e.g. diazoles, etc.
(1) Note. An example of an active ingredient provided for
herein is, [figure]
Subclass:
217.10
![[Patents]](../gifs/ps.gif)
Chalcogen is one of the ring hetero atoms:
Subject matter under 217.09 wherein one of the hetero atoms
in the additional hetero ring is a chalcogen (i.e. oxygen,
sulfur, selenium, or tellurium).
Subclass:
217.11
![[Patents]](../gifs/ps.gif)
Nitrogen or -C(=X)-, wherein X is chalcogen, bonded directly
to the seven- membered hetero ring:
This subclass is indented under subclass 212.01. Subject
matter wherein the seven-membered hetero ring is bonded
directly to .nitrogen or to a -C(=X)- group, wherein X is
chalcogen (i.e. oxygen, sulfur, selenium or tellurium).
Subclass:
217.12
![[Patents]](../gifs/ps.gif)
Nitrogen or C(=X), wherein X is chalcogen, attached
indirectly to the seven-membered hetero ring by acyclic
nonionic bonding:
This subclass is indented under subclass 212.01. Subject
matter wherein the seven-membered hetero ring is attached
indirectly by acyclic nonionic bonding to nitrogen or to a
C(=X) group, wherein X is chalcogen (i.e. oxygen, sulfur,
selenium or tellurium),
Subclass:
218
![[Patents]](../gifs/ps.gif)
Hetero ring is seven-membered consisting of two nitrogen and
five carbon atoms:
This subclass is indented under subclass 183. Subject matter
which contains a seven-membered heterocyclic ring consisting
of two nitrogen and five carbon atoms.
Subclass:
219
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the seven-membered hetero ring
as one of the cyclos:
This subclass is indented under subclass 218. Subject matter
wherein the seven-membered hetero ring is one of the cyclos
of a polycyclo ring system.
Subclass:
220
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the seven-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 219. Subject matter
wherein the polycyclo ring system consists of exactly three
rings.
Subclass:
221
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the seven-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 219. Subject matter
wherein the polycyclo ring system consists of exactly two
rings.
Subclass:
222.2
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered and includes at least nitrogen
and sulfur as ring members:
This subclass is indented under subclass 183. Subject matter
in which the hetero ring contains at least nitrogen and
sulfur as ring hetero atoms and is six-membered.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
222.5
![[Patents]](../gifs/ps.gif)
Three or more ring hetero atoms in the six-membered hetero
ring:
This subclass is indented under subclass 222.2. Subject
matter in which the six-membered hetero ring contains at
least three ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
222.8
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 222.5. Subject
matter in which the six-membered hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
223.2
![[Patents]](../gifs/ps.gif)
1,2,4,-benzothiadiazine-1, 1-dioxides (including
hydrogenated):
This subclass is indented under subclass 222.8. Subject
matter in which the polycyclo ring system has the following
basic structure, which may contain double bonds between ring
members: [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
223.5
![[Patents]](../gifs/ps.gif)
With additional active ingredient:
This subclass is indented under subclass 223.2. Subject
matter in which, in addition to the 1,2,
4-benzothiadiazine-1, 1-dioxide compound, an additional
active ingredient is present.
(1) Note. This subclass provides for subject matter wherein
plural nonidentical 1,2, 4-benzothiadiazine-1, 1-dioxide
compounds are each present as active ingredients.
Subclass:
223.8
![[Patents]](../gifs/ps.gif)
1,3,5-thiadiazines:
This subclass is indented under subclass 222.5. Subject
matter in which the six-membered hetero ring has the
following basic structure, which may contain double bonds
between ring members: [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
224.2
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the six-membered hetero ring as
one of the cyclos (e.g., 1,3- and 1,4-benzothiazines, etc.):
This subclass is indented under subclass 222.22. Subject
matter in which the six-membered hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
224.5
![[Patents]](../gifs/ps.gif)
At least three cyclos in the polycyclo ring system:
This subclass is indented under subclass 224.2. Subject
matter in which the polycyclo ring system contains three or
more cyclos.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
224.8
![[Patents]](../gifs/ps.gif)
Phenothiazines (including hydrogenated):
This subclass is indented under subclass 224.5. Subject
matter in which the polycyclo ring system has the following
basic structure, which may contain double bonds between ring
members: [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
225.2
![[Patents]](../gifs/ps.gif)
Hetero ring attached directly or indirectly to the
phenothiazine ring nitrogen by acyclic nonionic bonding:
This subclass is indented under subclass 224.8. Subject
matter in which the phenothiazine ring nitrogen is attached
directly or indirectly to a hetero ring by acyclic nonionic
bonding.
(1) Note. An example of a active ingredient provided for
herein is: [figure]
Subclass:
225.5
![[Patents]](../gifs/ps.gif)
The hetero ring is monocyclic piperidine:
This subclass is indented under subclass 225.2. Subject
matter in which monocyclic piperidine is the hetero ring.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
225.8
![[Patents]](../gifs/ps.gif)
The hetero ring contains plural ring nitrogens:
This subclass is indented under subclass 225.2. Subject
matter in which the hetero ring contains more than one ring
nitrogen.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
226.2
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen attached indirectly to the
phenothiazine ring nitrogen by acyclic nonionic bonding:
This subclass is indented under subclass 224.8. Subject
matter in which the phenothiazine ring nitrogen is attached
indirectly to chalcogen (i.e., oxygen, sulfur, selenium, or
tellurium) or to nitrogen by acyclic nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
226.5
![[Patents]](../gifs/ps.gif)
One of the cyclos is a 1, 2-thiazine (e.g., 1,
2-benzothiazines, etc.):
This subclass is indented under subclass 224.2. Subject
matter in which a 1, 2-thiazines is one of the cyclos of the
polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
226.8
![[Patents]](../gifs/ps.gif)
1, 3-thiazines:
This subclass is indented under subclass 222.2. Subject
matter in which the hetero ring has the following basic
structure, which may contain double bonds between ring
members: [figure]
(1) Note. An example of an ingredient provided for herein
is: [figure]
Subclass:
227.2
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly to ring carbon of the
six-membered hetero ring:
This subclass is indented under subclass 226.8. Subject
matter in which a ring carbon if the 1, 3-thiazine ring is
bonded directly to chalcogen (i.e., oxygen, sulfur, selenium,
or tellurium) or to nitrogen.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
227.5
![[Patents]](../gifs/ps.gif)
1, 4-thiazines:
This subclass is indented under subclass 222.2. Subject
matter in which the hetero ring has the following basic
structure, which may contain double bonds between ring
members: [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
227.8
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
1, 4-thiazine by nonionic bonding:
This subclass is indented under subclass 227.5. Subject
matter in which the 1, 4-thiazines is attached directly or
indirectly by nonionic bonding to an additional hetero ring.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
228.2
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional hetero ring as
one if the cyclos:
This subclass is indented under subclass 227.8. Subject
matter in which the additional hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
228.5
![[Patents]](../gifs/ps.gif)
Three or more ring hetero atoms in the polycyclo ring
system:
This subclass is indented under subclass 228.2. Subject
matter in which the polycyclo ring system contains at least
three ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
228.8
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered and includes at least nitrogen
and oxygen as ring hetero atoms (e.g., monocyclic 1, 2- and
1, 3-oxazines, etc.):
This subclass is indented under subclass 183. Subject matter
in which the hetero ring contains at least nitrogen and
oxygen as ring hetero atoms and is six-membered.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
229.2
![[Patents]](../gifs/ps.gif)
Three or more ring hetero atoms in the six-membered hetero
ring:
This subclass is indented under subclass 228.8. Subject
matter in which the six-membered hetero ring contains at
least three ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
229.5
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the six-membered hetero ring as
one of the cyclos (e.g., maytansinoids, etc.):
This subclass is indented under subclass 228.8. Subject
matter in which the six-membered hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
229.8
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 229.5. Subject
matter in which the six-membered hetero ring is one of the
cyclos of a tricyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
230.2
![[Patents]](../gifs/ps.gif)
Ring nitrogen shared by two of the cyclos:
This subclass is indented under subclass 229.8. Subject
matter in which the tricyclo ring system contains a ring
nitrogen which is shared by two of the cyclos.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
230.5
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the six-membered hetero ring as
one of the cyclos (e.g., 1 4-benzoxazines, etc.):
This subclass is indented under subclass 229.5. Subject
matter in which the six-membered hetero ring is one of the
cyclos of a bicyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
230.8
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of 1, 4-oxazine
ring:
This subclass is indented under subclass 228.8. Subject
matter in which the six-membered hetero ring has the
following basic structure which may contain double bonds
between ring members, as illustrated below, and in which
chalcogen (i.e., oxygen, sulfur, selenium, or tellurium) is
bonded directly to a ring carbon of the six-membered hetero
ring. [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
231.2
![[Patents]](../gifs/ps.gif)
Morpholines (i.e., fully hydrogenated 1, 4-oxazines):
This subclass is indented under subclass 228.8. Subject
matter in which the six-membered hetero ring has the
following basic structure: [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
231.5
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
morpholine ring by nonionic bonding:
This subclass is indented under subclass 231.2. Subject
matter in which the morpholine ring is attached to an
additional hetero ring by direct or indirect nonionic
bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
231.8
![[Patents]](../gifs/ps.gif)
Plural morpholine rings attached directly or indirectly to
each other by nonionic bonding:
This subclass is indented under subclass 231.5. Subject
matter in which the compound contains two or more morpholine
rings attached to each other by direct or indirect nonionic
bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
232.2
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
morpholines by nonionic bonding:
This subclass is indented under subclass 231.8. Subject
matter in which the morpholines are attached to an additional
hetero ring by direct or indirect nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
232.5
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional hetero ring as
one of the cyclos:
This subclass is indented under subclass 232.2. Subject
matter in which the additional hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
232.8
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional hetero ring as
one of the cyclos:
This subclass is indented under subclass 231.5. Subject
matter in which the additional hetero ring is one of the
cyclos of a polycyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
233.2
![[Patents]](../gifs/ps.gif)
Ring nitrogen shared by two of the cyclos:
This subclass is indented under subclass 232.8. Subject
matter in which two of the cyclos in the polycyclo ring
system share a ring nitrogen.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
233.5
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the additional hetero ring as one
of the cyclos:
This subclass is indented under subclass 232.8. Subject
matter in which the additional hetero ring is one of the
cyclos of a bicyclo ring system.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
233.8
![[Patents]](../gifs/ps.gif)
Plural ring hetero atoms in the bicyclo ring system:
This subclass is indented under subclass 233.5. Subject
matter in which the bicyclo ring system contains two or more
ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
234.2
![[Patents]](../gifs/ps.gif)
Three or more ring hetero atoms in the bicyclo ring system:
This subclass is indented under subclass 233.8. Subject
matter in which the bicyclo ring system contains at least
three ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
234.5
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens in the bicyclo ring system:
This subclass is indented under subclass 233.8. Subject
matter in which the bicyclo ring system contains two ring
nitrogens.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
234.8
![[Patents]](../gifs/ps.gif)
Quinoxalines (including hydrogenated):
This subclass is indented under subclass 234.5. Subject
matter in which the bicyclo ring system has the following
basic structure which may contain double bonds between ring
members: [figure]
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
235.2
![[Patents]](../gifs/ps.gif)
Ring nitrogen in the bicyclo ring system:
This subclass is indented under subclass 234.5. Subject
matter in which the bicyclo ring system contains a ring
nitrogen.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
235.5
![[Patents]](../gifs/ps.gif)
Ring nitrogen in the additional hetero ring:
This subclass is indented under subclass 231.5. Subject
matter in which the additional hetero ring contains a ring
nitrogen.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
235.8
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens in the additional hetero ring (e.g.,
imidazole, pyrazine, etc.):
This subclass is indented under subclass 235.5. Subject
matter in which the additional hetero ring contains plural
ring nitrogens.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
236.2
![[Patents]](../gifs/ps.gif)
Three or more ring hetero atoms in the additional hetero
ring:
This subclass is indented under subclass 235.8. Subject
matter in which the additional hetero ring contains at least
three ring hetero atoms.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
236.5
![[Patents]](../gifs/ps.gif)
The ring nitrogens are bonded directly to each other (e.g.,
pyridazine, etc.):
This subclass is indented under subclass 235.8. Subject
matter in immediately adjacent to each other in the ring.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
236.8
![[Patents]](../gifs/ps.gif)
Ring chalcogen in the additional hetero ring (e.g., oxazole,
etc.):
This subclass is indented under subclass 235.5. Subject
matter in which the additional hetero ring also contains a
ring chalcogen (i.e., oxygen, sulfur, selenium, or
tellurium).
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
237.2
![[Patents]](../gifs/ps.gif)
The additional hetero ring is attached indirectly to the
morpholine ring by an acyclic chain having a hetero atom as a
chain member:
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
237.5
![[Patents]](../gifs/ps.gif)
Having -C(=X)-, wherein X is chalcogen, bonded directly to
the morpholine ring:
This subclass is indented under subclass 231.2. Subject
matter in which the morpholine ring is bonded directly
to-C(=X)-, wherein X is chalcogen (i.e., oxygen, sulfur,
selenium, or tellurium).
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
237.8
![[Patents]](../gifs/ps.gif)
Nitrogen attached indirectly to the morpholine ring by
acyclic nonionic bonding:
This subclass is indented under subclass 231.2. Subject
matter in which the morpholine ring is attached indirectly to
nitrogen by acyclic nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
238.2
![[Patents]](../gifs/ps.gif)
Chalcogen attached directly to the nitrogen by nonionic
bonding:
This subclass is indented under subclass 237.8. Subject
matter in which the nitrogen is attached directly to
chalcogen (i.e., oxygen, sulfur, selenium, or tellurium) by
nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
238.5
![[Patents]](../gifs/ps.gif)
The nitrogen is double or triple bonded directly to carbon:
This subclass is indented under subclass 237.8. Subject
matter in which carbon is bonded directly to the nitrogen by
a double or triple bond.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
238.8
![[Patents]](../gifs/ps.gif)
Chalcogen attached indirectly to the morpholine ring by
acyclic nonionic bonding:
This subclass is indented under subclass 231.2. Subject
matter in which the morpholine ring is attached indirectly to
chalcogen (i.e., oxygen, sulfur, selenium, or tellurium) by
acyclic nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
239.2
![[Patents]](../gifs/ps.gif)
The chalcogen is bonded directly to two carbon atoms:
This subclass is indented under subclass 238.8. Subject
matter in which each of two carbon atoms is bonded directly
to the chalcogen.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
239.5
![[Patents]](../gifs/ps.gif)
Carbocyclic ring attached indirectly to the morpholine ring
by nonionic bonding:
This subclass is indented under subclass 231.2. Subject
matter in which the morpholine ring is attached indirectly to
a carbocyclic ring by nonionic bonding.
(1) Note. An example of an active ingredient provided for
herein is: [figure]
Subclass:
241
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered consisting of three nitrogens and
three carbon atoms:
This subclass is indented under subclass 183. Subject matter
wherein the active ingredient contains a six-membered
heterocyclic nucleus consisting of three nitrogen atoms and
three carbon atoms.
Subclass:
242
![[Patents]](../gifs/ps.gif)
Asymmetrical (e.g., 1,2,4-triazine, etc.):
This subclass is indented under subclass 241. Subject matter
wherein the heterocyclic ring is asymmetrical e.g., (1,2,4-
triazine) [figure] [caption], etc.
Subclass:
243
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 242. Subject matter
wherein the triazine is a part of a fused ring or bridged
ring system.
Subclass:
244
![[Patents]](../gifs/ps.gif)
Hexamethylenetetramines:
This subclass is indented under subclass 241. Subject matter
wherein the active ingredient comprises the following
structure (i.e., hexamethylenetertramines). [figure]
Subclass:
245
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to ring carbon of the hetero ring:
This subclass is indented under subclass 241. Subject matter
wherein the six-membered heterocyclic compound has nitrogen
bonded directly to at least one of the ring carbons.
Subclass:
246
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having a 1,3,5-triazine as one of the
cyclos:
This subclass is indented under subclass 241. Subject matter
wherein the six-membered heterocyclic compound is a
1,3,5-triazine which is a part of a fused ring or bridged
ring system.
Subclass:
247
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered consisting of two nitrogens and
four carbon atoms (e.g., pyridazines, etc.):
This subclass is indented under subclass 183. Subject matter
wherein the active ingredient has a six-membered heterocyclic
nucleus which consists of two nitrogen and four carbon atoms,
e.g., [figure] [caption], etc.
Subclass:
248
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having a 1,2-or 1,4-diazine as one of
the cyclos:
This subclass is indented under subclass 247. Subject matter
wherein the six-membered heterocyclic ring is a part of a
fused ring or bridged ring system wherein the two nitrogens
occupy the 1,2, or 1,4-positions of the diazine ring, e.g.,
[figure] [caption], etc.
Subclass:
249
![[Patents]](../gifs/ps.gif)
1,4-diazine as one of the cyclos:
This subclass is indented under subclass 248. Subject matter
wherein a 1,4-diazine ring is a part of the fused or bridged
ring system.
Subclass:
250
![[Patents]](../gifs/ps.gif)
At least three rings in the polycyclo ring system:
This subclass is indented under subclass 249. Subject matter
wherein the active ingredient is a tricyclo and has the
1,4-diazine nucleus as one of the cyclos, e.g., [figure]
[caption], etc.
Subclass:
251
![[Patents]](../gifs/ps.gif)
Isoalloxazine (e.g., riboflavins, vitamin B2, etc.):
This subclass is indented under subclass 250. Subject matter
in which the 1,4, diazine is part of a radical having the
following structure: [figure]
(1) Note. In a derivative, the ring structure and carbonyl
moieties must remain intact. Any position on the ring may be
substituted.
(2) Note. This subclass provides for a vitamin
B[subscrpt]2[end subscrpt] (or G) composition.
(3) Note. A patent with a claim directed to a riboflavin
composition will be placed here and not in subclass 23.
Subclass:
252.01
![[Patents]](../gifs/ps.gif)
1,2-diazines attached directly or indirectly to an additional
hetero ring by nonionic bonding:
This subclass is indented under subclass 247. Subject
matter wherein the six-membered hetero ring is a 1,2 diazine
ring which is attached directly or indirectly to an
additional hetero ring by nonionic bonding.
SEE OR SEARCH CLASS:
544, Carbon Compounds, subclasses 224-241 for compounds
which include a 1,2-diazine ring.
Subclass:
252.02
![[Patents]](../gifs/ps.gif)
The additional hetero ring is a diazine:
This subclass is indented under subclass 252.01. Subject
matter wherein the additional hetero ring is a six-membered
hetero ring consisting of two nitrogens and four carbon
atoms.
Subclass:
252.03
![[Patents]](../gifs/ps.gif)
The additional hetero ring is six-membered consisting of one
nitrogen and five carbon atoms:
This subclass is indented under subclass 252.01. Subject
matter wherein the additional hetero ring consists of five
carbon atoms and one nitrogen atom.
Subclass:
252.04
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional six-membered
hetero ring as one of the cyclos:
This subclass is indented under subclass 252.03. Subject
matter wherein the additional six-membered hetero ring is a
cyclo of a polycyclo ring system.
Subclass:
252.05
![[Patents]](../gifs/ps.gif)
The additional hetero ring is a five-membered nitrogen
containing hetero ring:
This subclass is indented under subclass 252.01. Subject
matter wherein the additional hetero ring has five members,
at least one of which is nitrogen.
Subclass:
252.06
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional five-membered
hetero ring as one of the cyclos:
This subclass is indented under subclass 252.05. Subject
matter wherein the additional nitrogen containing
five-membered hetero ring is a cyclo of a polycyclo ring
system.
Subclass:
252.1
![[Patents]](../gifs/ps.gif)
1,4 diazines:
This subclass is indented under subclass 247. Subject
matter wherein the six-membered hetero ring is a 1, 4-diazine
ring..
SEE OR SEARCH CLASS:
544, Carbon Compounds, subclasses 336-410, for compounds
which include a 1,4-diazine ring.
Subclass:
252.11
![[Patents]](../gifs/ps.gif)
Plural 1,4-diazine rings attached directly or indirectly to
each other by nonionic bonding:
This subclass is indented under subclass 252.10. Subject
matter wherein an additional 1,4-diazine ring is attached
directly or indirectly by nonionic bonding to the 1,4-diazine
ring.
Subclass:
252.12
![[Patents]](../gifs/ps.gif)
Piperazines (i.e. fully hydrogenated 1,4-diazines):
This subclass is indented under subclass 252.10. Subject
matter wherein the 1,4-diazine ring is fully saturated.
Subclass:
252.13
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
piperazine ring by nonionic bonding:
This subclass is indented under subclass 252.12. Subject
matter wherein the piperazine ring is attached directly or
indirectly to an additional hetero ring by nonionic bonding.
Subclass:
252.14
![[Patents]](../gifs/ps.gif)
The additional hetero ring is a 1,3-diazine ring:
This subclass is indented under subclass 252.13. Subject
matter wherein the additional hetero ring consists of four
carbon atoms and two nitrogens; the nitrogens are in the 1-
and 3- positions of the ring.
Subclass:
252.15
![[Patents]](../gifs/ps.gif)
Spiro ring system containing:
This subclass is indented under subclass 252.14. Subject
matter wherein the active ingredient containing the diazine
rings includes a spiro ring system.
(1) Note. Neither the 1,4-diazine ring nor the 1,3-diazine
ring has to be part of the spiro ring system.
Subclass:
252.16
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional 1,3-diazine ring
as one of the cyclos:
This subclass is indented under subclass 252.14. Subject
matter wherein the additional 1,3-diazine ring is a cyclo of
a polycyclo ring system.
Subclass:
252.17
![[Patents]](../gifs/ps.gif)
The polycyclo ring system is quinazoline (including
hydrogenated):
This subclass is indented under subclass 252.16. Subject
matter wherein the 1,3-diazine is part of a quinazoline ring
system, which may be hydrogenated.
Subclass:
252.18
![[Patents]](../gifs/ps.gif)
Additional six-membered hetero consisting of five ring
carbons and one ring nitrogen attached directly or indirectly
to the 1,3-diazine by nonionic bonding:
This subclass is indented under subclass 252.14. Subject
matter wherein the 1,3-diazine ring is attached directly or
indirectly by nonionic bonding to an additional six-membered
hetero ring that consists of five ring carbons and one ring
nitrogen.
Subclass:
252.19
![[Patents]](../gifs/ps.gif)
Five-membered nitrogen hetero ring attached directly or
indirectly to the 1,3-diazine ring by nonionic bonding:
This subclass is indented under subclass 252.14. Subject
matter wherein the 1,3-diazine ring is attached directly or
indirectly by nonionic bonding to an additional five-membered
nitrogen hetero ring.
Subclass:
252.2
![[Patents]](../gifs/ps.gif)
Oxygen hetero ring attached directly or indirectly to the
1,3-diazine ring by nonionic bonding:
This subclass is indented under subclass 252.14. Subject
matter wherein the 1,3 diazine ring is attached directly or
indirectly by nonionic bonding to a hetero ring having oxygen
as a ring member.
Subclass:
253.01
![[Patents]](../gifs/ps.gif)
The additional hetero ring is six-membered consisting of one
nitrogen and five carbon atoms:
This subclass is indented under subclass 252.13. Subject
matter wherein the additional hetero ring has exactly six
members and consists of five carbon atoms and one nitrogen
atom.
Subclass:
253.02
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional six-membered
nitrogen hetero ring as one of the cyclos:
This subclass is indented under subclass 253.01. Subject
matter wherein the additional six-membered hetero ring
consisting of five ring carbons and one ring nitrogen is a
cyclo of a polycyclo ring system.
Subclass:
253.03
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the additional six-membered
nitrogen hetero ring as one of the cyclos:
This subclass is indented under subclass 253.02. Subject
matter wherein the polycyclo ring system containing the
additional six-membered hetero ring consisting of five ring
carbons and one ring nitrogen has exactly three cyclos.
Subclass:
253.04
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the additional six-membered
nitrogen hetero ring as one of the cyclos:
This subclass is indented under subclass 253.02. Subject
matter wherein the polycyclo ring system containing the
additional six-membered hetero ring consisting of five ring
carbons and one ring nitrogen has exactly two cyclos.
Subclass:
253.05
![[Patents]](../gifs/ps.gif)
Isoquinolines (including hydrogenated):
This subclass is indented under subclass 253.04. Subject
matter wherein the bicyclo ring system is an isoquinoline
ring system, which may be hydrogenated.
Subclass:
253.06
![[Patents]](../gifs/ps.gif)
Quinolines (including hydrogenated):
This subclass is indented under subclass 253.04. Subject
matter wherein the bicyclo ring system is a quinoline ring
system which may be hydrogenated.
Subclass:
253.07
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to carbon of the hetero ring of the
quinoline ring system:
This subclass is indented under subclass 253.06. Subject
matter wherein a chalcogen atom (i.e. oxygen, sulfur,
selenium, or tellurium) is bonded directly to a ring carbon
of the hetero ring of the quinoline ring system.
Subclass:
253.08
![[Patents]](../gifs/ps.gif)
Having -C (=X)-, wherein X is chalcogen, bonded directly to
carbon of the hetero ring of thequinoline ring system:
This subclass is indented under subclass 253.07. Subject
matter wherein a -C(=X)- group, wherein X is chalcogen (i.e.
oxygen, sulfur, selenium, or tellurium), is bonded directly
to carbon of the hetero ring of the quinoline ring system.
Subclass:
253.09
![[Patents]](../gifs/ps.gif)
Five-membered nitrogen hetero ring attached directly or
indirectly to the piperazine ring by nonionic bonding:
This subclass is indented under subclass 253.01. Subject
matter wherein the piperazine ring is attached directly or
indirectly by nonionic bonding to a five-membered hetero ring
having ring nitrogen.
Subclass:
253.1
![[Patents]](../gifs/ps.gif)
The five-membered nitrogen hetero ring has chalcogen as a
ring member:
This subclass is indented under subclass 253.09. Subject
matter wherein the five-membered nitrogen hetero ring also
contains chalcogen (i.e. oxygen, sulfur, selenium, or
tellurium) as a member of the hetero ring.
Subclass:
253.11
![[Patents]](../gifs/ps.gif)
Chalcogen hetero ring attached directly or indirectly to the
piperazine ring by nonionic bonding:
This subclass is indented under subclass 253.01. Subject
matter wherein a hetero ring having chalcogen (i.e. oxygen,
sulfur, selenium, or tellurium) as a ring member is attached
directly or indirectly to the piperazine ring by nonionic
bonding.
Subclass:
253.12
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the additional
six-membered nitrogen containing hetero ring:
This subclass is indented under subclass 253.01. Subject
matter wherein the additional six-membered nitrogen
containing hetero ring consisting of five ring carbons and
one ring nitrogen has a chalcogen (i.e. oxygen, sulfur,
selenium, or tellurium) bonded directly to carbon of its
ring.
Subclass:
253.13
![[Patents]](../gifs/ps.gif)
Having -C (=X)-, wherein X is chalcogen, bonded directly to
the additional six-membered nitrogen hetero ring:
This subclass is indented under subclass 253.01. Subject
matter wherein the additional six-membered nitrogen hetero
ring consisting of five ring carbons and one ring nitrogen
has a -C(=X)- group, wherein X is chalcogen (i.e. oxygen,
sulfur, selenium, or tellurium), bonded directly thereto.
Subclass:
254.01
![[Patents]](../gifs/ps.gif)
The additional hetero ring is five-membered having ring
nitrogen:
This subclass is indented under subclass 252.13. Subject
matter wherein the additional hetero ring has exactly five
members, including ring nitrogen.
Subclass:
254.02
![[Patents]](../gifs/ps.gif)
The additional five-membered hetero ring also has chalcogen
as a ring member:
This subclass is indented under subclass 254.01. Subject
matter wherein nitrogen and chalcogen (i.e. oxygen, sulfur,
selenium, or tellurium) are ring members of the additional
five-membered hetero ring.
Subclass:
254.03
![[Patents]](../gifs/ps.gif)
The additional five-membered hetero ring consists of two ring
carbons, two ring nitrogens, and one ring chalcogen (e.g.,
oxadiazolyl, thiadiazolyl, etc.):
This subclass is indented under subclass 254.02. Subject
matter wherein the additional five-membered hetero ring has
two nitrogens and one chalcogen (i.e. oxygen, sulfur,
selenium, or tellurium) as the ring hetero atoms.
Subclass:
254.04
![[Patents]](../gifs/ps.gif)
The additional five-membered hetero ring consists of three
ring carbons, and of nitrogen and chalcogen in adjacent ring
positions (e.g., isoxaazolyl, isothiazolyl, etc.):
This subclass is indented under subclass 254.02. Subject
matter wherein one chalcogen (i.e. oxygen, sulfur, selenium,
or tellurium) and one nitrogen are adjacent ring members of
the additional five-membered hetero ring, and the remaining
ring members are carbon.
Subclass:
254.05
![[Patents]](../gifs/ps.gif)
Plural nitrogens in the additional five-membered hetero
ring:
This subclass is indented under subclass 254.01. Subject
matter wherein the additional five-membered hetero ring
contains at least two ring nitrogen atoms.
Subclass:
254.06
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the plural nitrogen containing
additional five-membered hetero ring as one of the cyclos:
This subclass is indented under subclass 254.05. Subject
matter wherein the additional plural nitrogen containing
five-membered hetero ring is a cyclo of a polycyclo ring
system.
Subclass:
254.07
![[Patents]](../gifs/ps.gif)
Chalcogen hetero ring attached directly or indirectly to the
piperazine ring by nonionic bonding:
This subclass is indented under subclass 254.05. Subject
matter wherein a chalcogen (i.e. oxygen, sulfur, selenium, or
tellurium) containing hetero ring is attached directly or
indirectly to the piperazine ring by nonionic bonding.
Subclass:
254.08
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional five-membered
nitrogen hetero ring as one of the cyclos:
This subclass is indented under subclass 254.01. Subject
matter wherein the five-membered hetero ring is a cyclo of a
ploycyclo ring system.
Subclass:
254.09
![[Patents]](../gifs/ps.gif)
Indole ring system (including hydrogenated) attached directly
or indirectly to the piperazine ring by nonionic bonding:
This subclass is indented under subclass 254.08. Subject
matter wherein the polycyclo ring system consists of exactly
two ortho-fused rings with the nitrogen being in the
1-position of the five-membered hetero ring, and the second
ring consisting of six carbon atoms.
Subclass:
254.1
![[Patents]](../gifs/ps.gif)
Ring oxygen in the additional hetero ring:
This subclass is indented under subclass 252.13. Subject
matter wherein the additional hetero ring has at least one
ring oxygen atom.
Subclass:
254.11
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the additional oxygen hetero
ring as one of the cyclos:
This subclass is indented under subclass 254.10. Subject
matter wherein the additional oxygen containing hetero ring
is a cyclo of a polycyclo ring system.
Subclass:
255.01
![[Patents]](../gifs/ps.gif)
Nitrogen or -C(=X)-, wherein X is chalcogen, bonded directly
to the piperazine ring:
This subclass is indented under subclass 252.12. Subject
matter wherein nitrogen or a -C(=X)- group, wherein X is
chalcogen (i.e., oxygen, sulfur, selenium, or tellurium), is
bonded directly to the piperazine ring.
Subclass:
255.02
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to a piperazine ring carbon:
This subclass is indented under subclass 252.12. Subject
matter wherein a chalcogen (i.e. oxygen, sulfur, selenium, or
tellurium) is bonded directly to carbon of the piperazine
ring.
Subclass:
255.03
![[Patents]](../gifs/ps.gif)
Carbocyclic ring bonded directly to the piperazine ring:
This subclass is indented under subclass 252.12. Subject
matter wherein the piperazine ring is bonded directly to a
carbocyclic ring.
Subclass:
255.04
![[Patents]](../gifs/ps.gif)
Plural carbocyclic rings bonded directly to the same acyclic
carbon atom which is attached directly or indirectly to the
piperazine ring by nonionic bonding:
This subclass is indented under subclass 252.12. Subject
matter wherein the piperazine ring is attached directly or
indirectly by nonionic bonding to an acyclic carbon atom
which is bonded to plural carbocyclic rings.
Subclass:
255.05
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
1,4-diazine ring by nonionic bonding:
This subclass is indented under subclass 252.10. Subject
matter wherein the 1,4-diazine ring is attached directly or
indirectly by nonionic bonding to an additional hetero ring
Subclass:
255.06
![[Patents]](../gifs/ps.gif)
Nitrogen or -C(=X)-, wherein X is chalcogen, bonded directly
to ring carbon of the 1,4- diazine ring:
This subclass is indented under subclass 252.10. Subject
matter wherein a ring carbon of the 1,4-diazine ring is
bonded directly to a nitrogen atom or a -C(=X)- group,
wherein X is chalcogen (i.e., oxygen, sulfur, selenium, or
tellurium).
Subclass:
256
![[Patents]](../gifs/ps.gif)
1,3-diazines (e.g., pyrimidines, etc.):
This subclass is indented under subclass 247. Subject matter
in which the ring nitrogen atoms occupy the 1,3 positions of
the diazine nucleus i.e., [figure]
Subclass:
257
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having 1,3-diazine as one of the
cyclos:
This subclass is indented under subclass 256. Subject matter
in which the 1,3 - diazine is a part of a polycyclo ring
system, e.g., [figure] [caption], etc.
Subclass:
258
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having 1,3-diazine as one of the cyclos:
This subclass is indented under subclass 257. Subject matter
in which the polycyclo is a bicyclo.
Subclass:
259
![[Patents]](../gifs/ps.gif)
Quinazolines (including hydrogenated):
This subclass is indented under subclass 258. Subject matter
which contains the quinazoline nucleus, i.e., as illustrated
below, or hydrogenated forms thereof. [figure]
Subclass:
260
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to the 1,3-diazine at 2-position:
This subclass is indented under subclass 259. Subject matter
wherein a nitrogen is directly bonded to the 2-position of
the quinazoline nucleus, e.g., [figure] [figure] [caption],
etc.
Subclass:
261
![[Patents]](../gifs/ps.gif)
Purines (including hydrogenated):
This subclass is indented under subclass 258. Subject matter
wherein the active ingredient contains the purine nucleus,
i.e., as illustrated below, or hydrogenated forms thereof.
[figure]
Subclass:
262
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to a ring carbon of the purine:
This subclass is indented under subclass 261. Subject matter
wherein a chalcogen is directly bonded to a ring carbon of
the purine nucleus, e.g., [figure] [caption], etc.
Subclass:
263
![[Patents]](../gifs/ps.gif)
At both 2- and 6-positions (e.g., theophylline, etc.):
This subclass is indented under subclass 262. Subject matter
wherein carbons in the 2,6-positions of the purine nucleus
are each bonded to chalcogen, e.g., xanthine, caffeine,
theobromine, theophylline, etc.
Subclass:
264
![[Patents]](../gifs/ps.gif)
With an additional active ingredient or stabilizer:
This subclass is indented under subclass 263. Subject matter
wherein another active ingredient or stabilizing agent for
the purine compound is present in the composition.
Subclass:
265
![[Patents]](../gifs/ps.gif)
Additional hetero ring:
This subclass is indented under subclass 263. Subject matter
wherein the purine compound contains a substituent which is a
heterocyclic ring or contains a heterocyclic ring.
Subclass:
266
![[Patents]](../gifs/ps.gif)
Additional hetero ring:
This subclass is indented under subclass 261. Subject matter
wherein the purine compound has a substituent which is a
heterocyclic ring or contains a heterocyclic ring.
Subclass:
267
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having 1,3-diazine as one of the
cyclos:
This subclass is indented under subclass 257. Subject matter
wherein the 1,3-diazine is a part of a tricyclo ring system.
Subclass:
268
![[Patents]](../gifs/ps.gif)
Perimidines (including hydrogenated):
This subclass is indented under subclass 267. Subject matter
wherein the active ingredient contains the following
structure: [figure]
Subclass:
269
![[Patents]](../gifs/ps.gif)
Pyrimidines with chalcogen bonded directly to a ring carbon
of said pyrimidine moiety:
This subclass is indented under subclass 256. Subject matter
wherein the 1,3-diazine has a chalcogen bonded directly to a
ring carbon thereof, e.g., [figure] [caption], etc.
Subclass:
270
![[Patents]](../gifs/ps.gif)
Barbituric acid or derivative (including thioanalogs):
This subclass is indented under subclass 269. Subject matter
wherein the 1,3-diazine is of the structure, illustrated
below, wherein X is oxygen or sulfur or the enol form thereof
and R and/or R' are hydrogen, alkyl or aryl. [figure]
(1) Note. For this subclass, the three keto groups must be
present on the 1,3 diazine ring.
Subclass:
271
![[Patents]](../gifs/ps.gif)
Two or more barbituric acid compounds or with an additional
active ingredient or stabilizer:
This subclass is indented under subclass 270. Subject matter
which contains two or more compounds each having the moiety,
as shown below, or one compound having said moiety and an
additional organic active ingredient or stabilizing agent.
[figure]
(1) Note. Included herein is the combination of barbituric
acid and a salt thereof and complexes of two or more active
ingredients, or active ingredient complexed with stabilizing
agent.
(2) Note. Potentiating and synergistic agents are
considered active ingredients.
(3) Note. See section II, Glossary, for the definition of a
stabilizing agent.
Subclass:
272
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to the 1,3-diazine at 2-position:
This subclass is indented under subclass 269. Subject matter
wherein a nitrogen is bonded directly to the 1,3-diazine at
the 2- position, e.g., [figure] [caption], etc.
Subclass:
273
![[Patents]](../gifs/ps.gif)
The nitrogen is part of a hetero ring:
This subclass is indented under subclass 272. Subject matter
wherein the nitrogen is a part of a heterocyclic ring, e.g.,
[figure] [caption], etc.
Subclass:
274
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to pyrimidine at 2-position:
This subclass is indented under subclass 269. Subject matter
wherein a chalcogen is directly bonded to the 2-position of
the pyrimidine.
(1) Note. This subclass includes for example: [figure]
[caption], etc.
Subclass:
275
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to the 1,3-diazine at 2-position by
a single bond:
This subclass is indented under subclass 256. Subject matter
wherein the nitrogen is directly bonded to the 1,3-diazine at
the 2-position by a single bond.
Subclass:
276
![[Patents]](../gifs/ps.gif)
Thiamines (e.g., vitamin B1. etc.):
This subclass is indented under subclass 256. Subject matter
wherein the 1,3 diazine compound contains the structure, as
shown below, e.g., vitamin B1, etc. [figure]
Subclass:
277
![[Patents]](../gifs/ps.gif)
Hetero ring is six-membered consisting of one nitrogen and
five carbon atoms:
This subclass is indented under subclass 183. Subject matter
which contains a six-membered heterocyclic ring consisting of
one nitrogen and five carbon atoms.
Subclass:
278
![[Patents]](../gifs/ps.gif)
Spiro ring system:
This subclass is indented under subclass 277. Subject matter
which contains a spiro ring system.
Subclass:
279
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 277. Subject matter
wherein the six-membered hetero ring is one of the cyclos of
a polycyclo ring system.
Subclass:
280
![[Patents]](../gifs/ps.gif)
Pentacyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 279. Subject matter
wherein the polycyclo ring system consists of exactly five
rings.
Subclass:
281
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring members, (i.e.,
bridged):
This subclass is indented under subclass 280. Subject matter
wherein two cyclos of the polycyclo ring system share at
least three ring members.
Subclass:
282
![[Patents]](../gifs/ps.gif)
One of the five cyclos is five-membered and includes ring
chalcogen (e.g., codeine, morphine, etc.):
This subclass is indented under subclass 281. Subject matter
wherein one of the pentacyclo ring system is a five-membered
hetero ring which contains ring chalcogen, (i.e., oxygen,
sulfur, selenium or tellurium).
Subclass:
283
![[Patents]](../gifs/ps.gif)
Ring nitrogen in the pentacyclo ring system is shared by
five-membered cyclo and six-membered cyclo (e.g., vincamine,
etc.):
This subclass is indented under subclass 280. Subject matter
wherein the ring nitrogen of the six-membered hetero ring is
additionally a member of a five-membered cyclo in the
pentacyclo ring system.
Subclass:
284
![[Patents]](../gifs/ps.gif)
Tetracyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 279. Subject matter
wherein the polycyclo ring system consists of exactly four
rings.
Subclass:
285
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the tetracyclo ring system (e.g.,
acronycines, etc.):
This subclass is indented under subclass 284. Subject matter
wherein the tetracyclo ring system contains at least one ring
hetero atom in addition to the ring nitrogen of the
six-membered hetero ring.
Subclass:
286
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring members (i.e.,
bridged):
This subclass is indented under subclass 286. Subject matter
wherein two cyclos of the polycyclo ring system share at
least three ring members.
Subclass:
287
![[Patents]](../gifs/ps.gif)
Three or more hetero atoms in the tetracyclo ring system:
This subclass is indented under subclass 285. Subject matter
wherein the tetracyclo ring system contains at least two ring
hetero atoms in addition to the ring nitrogen of the
six-membered hetero ring.
Subclass:
288
![[Patents]](../gifs/ps.gif)
Ring carbon is shared by three of the cyclos:
This subclass is indented under subclass 285. Subject matter
wherein one ring carbon is a member of three of the cyclos in
the tetracyclo ring system (i.e., peri-fusion).
Subclass:
289
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring members (i.e.,
bridged) (e.g., morphinans etc.):
This subclass is indented under subclass 284. Subject matter
wherein two cyclos of the polycyclo ring system share at
least three ring carbons.
Subclass:
290
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 279. Subject matter
wherein the polycyclo ring system consists of exactly three
rings.
Subclass:
291
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the tricyclo ring system:
This subclass is indented under subclass 290. Subject matter
wherein the tricyclo ring system contains at least one ring
hetero atom in addition to the ring nitrogen of the
six-membered hetero ring.
Subclass:
292
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens in the tricyclo ring system:
This subclass is indented under subclass 291. Subject matter
wherein the tricyclo ring system contains at least two ring
nitrogens.
Subclass:
293
![[Patents]](../gifs/ps.gif)
Three or more hetero atoms in the tricyclo ring system:
This subclass is indented under subclass 292. Subject matter
wherein the tricyclo ring system contains at least three ring
hetero atoms.
Subclass:
294
![[Patents]](../gifs/ps.gif)
Ring nitrogen is shared by two of the cyclos:
This subclass is indented under subclass 290. Subject matter
wherein a ring nitrogen is a member of two of the cyclos in
the tricyclo ring system.
Subclass:
295
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring carbons (i.e.,
bridged) (e.g., benzomorphans, etc.):
This subclass is indented under subclass 290. Subject matter
wherein two cyclos of the polycyclo ring system share at
least three ring carbons.
Subclass:
296
![[Patents]](../gifs/ps.gif)
Ring carbon is shared by each of the three cyclos (e.g.,
1,8-naphthalimides, etc.):
This subclass is indented under subclass 290. Subject matter
wherein a ring carbon is a member of each of the cyclos of
the tricyclo ring system.
Subclass:
297
![[Patents]](../gifs/ps.gif)
Acridines (including hydrogenated):
This subclass is indented under subclass 290. Subject matter
wherein the tricyclo ring system has the following basic
structure, which may contain double bonds between ring
members: [figure]
Subclass:
298
![[Patents]](../gifs/ps.gif)
Phenathridines (including hydrogenated):
This subclass is indented under subclass 290. Subject matter
wherein the tricyclo ring system has the following structure,
which may contain double bonds between ring members:
[figure]
Subclass:
299
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the six-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 279. Subject matter
wherein the polycyclo ring system consists of exactly two
ring.
Subclass:
300
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the bicyclo ring system:
This subclass is indented under subclass 299. Subject matter
wherein the bicyclo ring system includes at least one ring
hetero atom in addition to the ring nitrogen of the
six-membered hetero ring.
Subclass:
301
![[Patents]](../gifs/ps.gif)
Ring sulfur in the bicyclo ring system:
This subclass is indented under subclass 300. Subject matter
wherein the bicyclo ring system contains ring sulfur.
Subclass:
302
![[Patents]](../gifs/ps.gif)
Ring oxygen in the bicyclo ring system:
This subclass is indented under subclass 300. Subject matter
wherein the bicyclo ring system contains ring oxygen.
Subclass:
303
![[Patents]](../gifs/ps.gif)
Exactly three ring nitrogens in the bicyclo ring system:
This subclass is indented under subclass 300. Subject matter
wherein the bicyclo ring system contains exactly three ring
nitrogens.
Subclass:
304
![[Patents]](../gifs/ps.gif)
Tropanes (including nor or dehydro forms):
This subclass is indented under subclass 299. Subject matter
wherein the bicyclo ring system has the following basic
structure: [figure]
Subclass:
305
![[Patents]](../gifs/ps.gif)
Quinuclidines (including unsaturation):
This subclass is indented under subclass 299. Subject matter
wherein the bicyclo ring system has the following basic
structure, which may contain double bonds between ring
members: [figure]
Subclass:
306
![[Patents]](../gifs/ps.gif)
Quinolizines (including hydrogenated):
This subclass is indented under subclass 299. Subject matter
wherein the bicyclo ring system has the following basic
structure, which may contain double bonds between ring
members: [figure]
Subclass:
307
![[Patents]](../gifs/ps.gif)
Isoquinolines (including hydrogenated):
This subclass is indented under subclass 299. Subject matter
wherein the bicyclo ring system has the following structure,
which may contain double bonds between ring members.
[figure]
Subclass:
308
![[Patents]](../gifs/ps.gif)
Plural isoquinoline ring systems attached directly or
indirectly to each other by nonionic bonding:
This subclass is indented under subclass 307. Subject matter
which contains at least two isoquinoline ring systems that
are attached directly or indirectly to each other by nonionic
bonding.
Subclass:
309
![[Patents]](../gifs/ps.gif)
Chalcogen attached directly to the six-membered hetero ring
by nonionic bonding:
This subclass is indented under subclass 307. Subject matter
wherein chalcogen (i.e., oxygen, sulfur, selenium or
tellurium) is attached directly to the six-membered hetero
ring of the isoquinoline ring system by nonionic bonding.
Subclass:
310
![[Patents]](../gifs/ps.gif)
Nitrogen, other than as nitro or nitroso, attached directly
to the isoquinoline ring system by nonionic bonding:
This subclass is indented under subclass 307. Subject matter
wherein nitrogen, except as a member of the nitro
(-NO[subscrpt]2[end subscrpt]) or nitroso (-NO) group, is
attached directly to the isoquinoline ring system by nonionic
bonding.
Subclass:
311
![[Patents]](../gifs/ps.gif)
Quinolines (including hydrogenated):
This subclass is indented under subclass 299. Subject matter
wherein the bicyclo ring system has the following basic
structure, which may contain double bonds between ring
members: [figure]
Subclass:
312
![[Patents]](../gifs/ps.gif)
Chalcogen attached directly to the six-membered hetero ring
by nonionic bonding:
This subclass is indented under subclass 311. Subject matter
wherein chalcogen (i.e., oxygen, sulfur, selenium or
tellurium) is attached directly to the six-membered hetero
ring of the quinoline ring system by nonionic bonding.
Subclass:
313
![[Patents]](../gifs/ps.gif)
Nitrogen, other than as nitro or nitroso, attached directly
to the six-membered hetero ring by nonionic bonding:
This subclass is indented under subclass 311. Subject matter
wherein nitrogen, except as a member of the nitro
(-NO[subscrpt]2[end subscrpt]) or nitroso (-NO) group, is
attached directly to the six-membered hetero ring of the
quinoline ring by nonionic bonding.
Subclass:
314
![[Patents]](../gifs/ps.gif)
Additional hetero ring attached directly or indirectly to the
quinoline ring system by nonionic bonding:
This subclass is indented under subclass 311. Subject matter
wherein a hetero ring is attached directly or indirectly to
the quinoline ring system by nonionic bonding.
(1) Note. Included herein are compounds which contain at
least two quinoline ring systems that are attached directly
or indirectly to each other by nonionic bonding.
Subclass:
315
![[Patents]](../gifs/ps.gif)
Piperidines:
This subclass is indented under subclass 277. Subject matter
wherein the six-membered hetero ring, consisting of one
nitrogen and five carbons, contains no double bonds between
ring members, i.e., the piperidine ring.
Subclass:
316
![[Patents]](../gifs/ps.gif)
Plural piperidine rings:
This subclass is indented under subclass 315. Subject matter
wherein the compound contains at least two piperidine rings.
Subclass:
317
![[Patents]](../gifs/ps.gif)
Additional ring containing:
This subclass is indented under subclass 315. Subject matter
which contains an additional ring.
Subclass:
318
![[Patents]](../gifs/ps.gif)
The additional ring is a six-membered hetero ring consisting
of one nitrogen and five carbon atoms:
This subclass is indented under subclass 317. Subject matter
wherein the additional ring is a pyridine ring or partially
hydrogenated pyridine ring.
Subclass:
319
![[Patents]](../gifs/ps.gif)
The additional ring is one of the cyclos in a polycyclo ring
system:
This subclass is indented under subclass 317. Subject matter
wherein the additional ring is one of the cyclos in a
polycyclo ring system.
Subclass:
320
![[Patents]](../gifs/ps.gif)
Hetero ring in the polycyclo ring system:
This subclass is indented under subclass 319. Subject matter
wherein the polycyclo ring system contains a hetero ring.
Subclass:
321
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the polycyclo ring system:
This subclass is indented under subclass 320. Subject matter
wherein the polycyclo ring system contains at least two ring
hetero atoms.
Subclass:
322
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens in the polycyclo ring system:
This subclass is indented under subclass 321. Subject matter
wherein the polycyclo ring system contains at least two ring
nitrogen atoms.
Subclass:
323
![[Patents]](../gifs/ps.gif)
Ring nitrogen in the polycyclo ring system:
This subclass is indented under subclass 320. Subject matter
wherein the polycyclo ring system contains a ring nitrogen.
Subclass:
324
![[Patents]](../gifs/ps.gif)
Ring sulfur in the polycyclo ring system:
This subclass is indented under subclass 320. Subject matter
wherein the polycyclo ring system contains a ring sulfur.
Subclass:
325
![[Patents]](../gifs/ps.gif)
Polycyclo ring system is tricyclo-carbocyclic:
This subclass is indented under subclass 319. Subject matter
wherein the polycyclo ring system consists of three
carbocyclic rings.
Subclass:
326
![[Patents]](../gifs/ps.gif)
The additional ring is a hetero ring:
This subclass is indented under subclass 317. Subject matter
wherein the additional ring is a hetero ring.
Subclass:
327
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the piperidine
ring:
This subclass is indented under subclass 317. Subject matter
wherein chalcogen (i.e., oxygen, sulfur, selenium or
tellurium) is bonded directly to a ring carbon of the
piperidine ring.
Subclass:
328
![[Patents]](../gifs/ps.gif)
Plural chalcogens bonded directly to ring carbons of the
piperidine ring:
This subclass is indented under subclass 327. Subject matter
wherein at least two chalcogens (i.e., oxygen, sulfur,
selenium or tellurium) are bonded directly to ring carbons of
the piperidine rings.
Subclass:
329
![[Patents]](../gifs/ps.gif)
Nitrogen attached directly to the piperidine ring by nonionic
bonding:
This subclass is indented under subclass 317. Subject matter
wherein nitrogen is attached directly to the piperidine ring
by nonionic bonding.
Subclass:
330
![[Patents]](../gifs/ps.gif)
C=X bonded directly to the piperidine ring (X is chalcogen):
This subclass is indented under subclass 317. Subject matter
wherein a C=O, C=S, C=Se or C=Te group is bonded directly to
the piperidine ring.
Subclass:
331
![[Patents]](../gifs/ps.gif)
Nitrogen attached indirectly to the piperidine ring nonionic
bonding:
This subclass is indented under subclass 317. Subject matter
wherein nitrogen is attached indirectly to the piperidine
ring by nonionic bonding.
Subclass:
332
![[Patents]](../gifs/ps.gif)
Plural six-membered hetero rings consisting of one nitrogen
and five carbon atoms:
This subclass is indented under subclass 277. Subject matter
which contains at least two of the six-membered hetero rings,
each consisting of one nitrogen and five carbons and having
at least one double bond between ring members, i.e., pyridine
or partially hydrogenated pyridine rings.
Subclass:
333
![[Patents]](../gifs/ps.gif)
Additional hetero ring other than the six-membered hetero
rings:
This subclass is indented under subclass 332. Subject matter
containing an additional hetero ring other than the
six-membered hetero rings consisting of one nitrogen and five
carbon atoms.
Subclass:
334
![[Patents]](../gifs/ps.gif)
The six-membered rings are bonded directly to each other:
This subclass is indented under subclass 332. Subject matter
wherein pyridine or partially hydrogenated pyridine rings are
bonded directly to each other.
Subclass:
335
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to a ring carbon of the
six-membered hetero ring:
This subclass is indented under subclass 332. Subject matter
wherein chalcogen (i.e., oxygen sulfur, selenium, tellurium)
is bonded directly to a ring carbon of a pyridine or
partially hydrogenated pyridine ring.
Subclass:
336
![[Patents]](../gifs/ps.gif)
Additional hetero ring containing:
This subclass is indented under subclass 277. Subject matter
which contains an additional hetero ring in the compound
other than the six-membered hetero ring consisting of one
nitrogen and five carbons, i.e., an additional hetero ring
other than a pyridine or partially hydrogenated pyridine
ring.
Subclass:
337
![[Patents]](../gifs/ps.gif)
The additional hetero ring is one of the cyclos in a
polycyclo ring system:
This subclass is indented under subclass 336. Subject matter
wherein the additional hetero ring is one of the cyclos in a
polycyclo ring system.
Subclass:
338
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the polycyclo ring system:
This subclass is indented under subclass 337. Subject matter
wherein the polycyclo ring system contains at least two ring
hetero atoms.
Subclass:
339
![[Patents]](../gifs/ps.gif)
Ring nitrogen in the polycyclo ring system:
This subclass is indented under subclass 337. Subject matter
wherein the polycyclo ring system contains one ring
nitrogen.
Subclass:
340
![[Patents]](../gifs/ps.gif)
Ring nitrogen in the additional hetero ring (e.g., oxazole,
etc.):
This subclass is indented under subclass 336. Subject matter
wherein the additional hetero ring contains ring nitrogens.
Subclass:
341
![[Patents]](../gifs/ps.gif)
The additional hetero ring consists of two nitrogens and
three carbons:
This subclass is indented under subclass 340. Subject matter
wherein the additional hetero ring consists of two nitrogens
and three carbons.
Subclass:
342
![[Patents]](../gifs/ps.gif)
Ring sulfur in the additional hetero ring:
This subclass is indented under subclass 340. Subject matter
wherein the additional hetero ring contains ring sulfur.
Subclass:
343
![[Patents]](../gifs/ps.gif)
The additional hetero ring consists of one nitrogen and four
carbons (e.g., nicotine, etc.):
This subclass is indented under subclass 340. Subject matter
wherein the additional hetero ring consists of one nitrogen
and four carbon atoms.
Subclass:
344
![[Patents]](../gifs/ps.gif)
Cyano bonded directly to the six-membered hetero ring:
This subclass is indented under subclass 277. Subject matter
which contains the -C=N group bonded directly to the
six-membered hetero ring.
Subclass:
345
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the six-membered
hetero ring:
This subclass is indented under subclass 277. Subject matter
wherein chalcogen (i.e., oxygen, sulfur, selenium or
tellurium) is bonded directly to a ring carbon of the
six-membered hetero ring.
Subclass:
346
![[Patents]](../gifs/ps.gif)
Chalcogen and cyclic nitrogen bonded directly to the same
carbon:
This subclass is indented under subclass 345. Subject matter
wherein chalcogen (i.e., oxygen, sulfur, selenium or
tellurium) and acyclic nitrogen are bonded directly to the
same carbon.
Subclass:
347
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to chalcogen:
This subclass is indented under subclass 345. Subject matter
wherein chalcogen (i.e., oxygen, sulfur, selenium or
tellurium) is bonded directly to chalcogen.
Subclass:
348
![[Patents]](../gifs/ps.gif)
Chalcogens bonded directly to at least two ring carbons of
the six-membered hetero ring:
This subclass is indented under subclass 345. Subject matter
wherein chalcogens (i.e., oxygen, sulfur, selenium or
tellurium) are bonded directly to at least two ring carbons
of the six-membered hetero ring.
Subclass:
349
![[Patents]](../gifs/ps.gif)
Nitrogen attached directly to the six-membered hetero ring by
nonionic bonding:
This subclass is indented under subclass 345. Subject matter
wherein nitrogen is attached directly to the six-membered
hetero ring by nonionic bonding.
Subclass:
350
![[Patents]](../gifs/ps.gif)
C=O bonded directly to the six-membered hetero ring:
This subclass is indented under subclass 345. Subject matter
wherein a C=O group is bonded directly to the six-membered
hetero ring.
Subclass:
351
![[Patents]](../gifs/ps.gif)
Nitrogen attached indirectly to the six-membered hetero ring
by nonionic bonding:
This subclass is indented under subclass 345. Subject matter
wherein nitrogen is attached indirectly to the six-membered
hetero ring by nonionic bonding.
Subclass:
352
![[Patents]](../gifs/ps.gif)
Nitrogen attached directly to the six-membered hetero ring by
nonionic bonding:
This subclass is indented under subclass 277. Subject matter
wherein nitrogen is attached directly to the six-membered
hetero ring by nonionic bonding.
Subclass:
353
![[Patents]](../gifs/ps.gif)
Plural acyclic nitrogens bonded directly to the same carbon
or bonded directly to each other:
This subclass is indented under subclass 352. Subject matter
wherein at least two acyclic nitrogens are bonded directly to
the same carbon or single bonded directly to each other.
Subclass:
354
![[Patents]](../gifs/ps.gif)
C=O bonded directly to the six-membered hetero ring:
This subclass is indented under subclass 277. Subject matter
wherein a C=O group is bonded directly to the six-membered
hetero ring.
Subclass:
355
![[Patents]](../gifs/ps.gif)
At 3-position:
This subclass is indented under subclass 354. Subject matter
wherein the C=O group is attached directly to the 3-position
of the six-membered hetero ring e.g., [figure] [caption],
etc.
Subclass:
356
![[Patents]](../gifs/ps.gif)
C=O in a C(=O)O group (e.g., nicotinic acid, etc.):
This subclass is indented under subclass 355. Subject matter
wherein the C=O is part of aO group.
Subclass:
357
![[Patents]](../gifs/ps.gif)
Nitrogen attached indirectly to the six-membered hetero ring
by nonionic bonding:
This subclass is indented under subclass 277. Subject matter
wherein nitrogen is attached indirectly to the six-membered
hetero ring by nonionic bonding.
Subclass:
358
![[Patents]](../gifs/ps.gif)
The ring nitrogen of the six-membered hetero ring is
pentavalent (e.g., quaternary pyridinium salts, etc.):
This subclass is indented under subclass 277. Subject matter
wherein the ring nitrogen of the six-membered ring is
pentavalent.
(1) Note. Examples of compounds provided for herein are:
[figure] [figure] [caption], etc.
Subclass:
359
![[Patents]](../gifs/ps.gif)
Five-membered hetero ring containing at least one nitrogen
ring atom (e.g., 1,2,3-triazoles, etc.):
This subclass is indented under subclass 183. Subject matter
wherein the hetero ring is five-membered and contains at
least one ring nitrogen, e.g., 1,2,3-triazoles, etc.
Subclass:
360
![[Patents]](../gifs/ps.gif)
Plural ring chalcogens in the hetero ring:
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring contains at least two
ring chalcogen atoms in addition to the ring nitrogen and
ring carbon, etc., 1,2,4-dithiazoles, etc.
Subclass:
361
![[Patents]](../gifs/ps.gif)
Plural ring nitrogens and a single chalcogen in the hetero
ring:
This subclass is indented under subclass 359. Subject matter
wherein the five-member hetero ring contains at least two
ring nitrogens and only one ring chalcogen.
Subclass:
362
![[Patents]](../gifs/ps.gif)
1,2,5-thiadiazoles (including hydrogenated):
This subclass is indented under subclass 361. Subject matter
wherein the hetero ring is 1,2,5-thiadiazole having the
following structure, as illustrated below, or hydrogenated
form thereof. [figure]
Subclass:
363
![[Patents]](../gifs/ps.gif)
1,3,4,-thiadiazoles (including hydrogenated):
This subclass is indented under subclass 361. Subject matter
wherein the hetero ring is 1,3,4,-Thiadiazole having the
following structure, as illustrated below, or hydrogenated
form thereof. [figure]
Subclass:
364
![[Patents]](../gifs/ps.gif)
Oxadiazoles (including hydrogenated):
This subclass is indented under subclass 361. Subject matter
wherein the hetero ring contains one ring oxygen and two ring
nitrogens as the only hetero atoms of the ring and may have a
double bond between ring members, e.g., [figure] [caption],
etc.
Subclass:
365
![[Patents]](../gifs/ps.gif)
1,2-thiazoles (including hydrogenated):
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is a 1,3-thiazole ring
which includes the following basic ring structure, as
illustrated below, and may contain a double bond between ring
members. [figure]
(1) Note. See section II, Glossary, for the definition of
"including hydrogenated".
Subclass:
366
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the thiazole ring as one of the
cyclos:
This subclass is indented under subclass 365. Subject matter
wherein the 1,3-thiazole ring is a cyclo of a polycyclo ring
system.
Subclass:
367
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the thiazole ring as one of the
cyclos:
This subclass is indented under subclass 366. Subject matter
wherein the polycyclo ring system consists of exactly two
rings.
Subclass:
368
![[Patents]](../gifs/ps.gif)
Ring nitrogen is shared by the cyclos of the bicyclo ring
system (e.g., tetramisole, etc.):
This subclass is indented under subclass 367. Subject matter
wherein the ring nitrogen is a member of both of the cyclos
in the bicyclo ring system, e.g., tetramisole etc.
Subclass:
369
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the thiazole
ring:
This subclass is indented under subclass 365. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
1,3-thiazole ring.
Subclass:
370
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly ring carbon of the thiazole ring:
This subclass is indented under subclass 365. Subject matter
wherein nitrogen is bonded directly to ring carbon of the
1,3-thiazole ring.
Subclass:
371
![[Patents]](../gifs/ps.gif)
C=X bonded directly to the nitrogen which is bonded directly
to the thiazole ring (X is chalcogen):
This subclass is indented under subclass 370. Subject matter
wherein the nitrogen is bonded additionally directly to a C=O
or C=S group.
Subclass:
372
![[Patents]](../gifs/ps.gif)
1,2-thiazoles (including hydrogenated):
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is a 1,2-thiazole ring
which includes the following basic ring structure,
illustrated below, and may contain a double bond between ring
members. [figure]
(1) Note. See section II, Glossary, for the definition of
"including hydrogenated".
Subclass:
373
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the thiazole ring as one of the
cyclos:
This subclass is indented under subclass 372. Subject matter
wherein the 1,2-thiazole ring is a cyclo of a polycyclo ring
system.
Subclass:
374
![[Patents]](../gifs/ps.gif)
1,3-oxazoles (including hydrogenated):
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is a 1,3-oxazole ring
which includes the following basic ring structure,
illustrated below, and may contain a double bond between ring
members. [figure]
(1) Note. See section II, Glossary, for the definition
"including hydrogenated".
Subclass:
375
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the oxazole ring as one of the
cyclos:
This subclass is indented under subclass 374. Subject matter
wherein the 1,3-oxazole ring is a cyclo of a polycyclo ring
system.
Subclass:
376
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the oxazole
ring:
This subclass is indented under subclass 374. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
1,3-oxazole ring.
Subclass:
377
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to ring carbon of the oxazole ring:
This subclass is indented under subclass 374. Subject matter
wherein nitrogen is bonded directly to ring carbon of the
1,3-oxazole ring.
Subclass:
378
![[Patents]](../gifs/ps.gif)
1,2-oxazoles (including hydrogenated):
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is a 1,2-oxazole ring
which includes the following basic ring structure,
illustrated below, and may contain a double bond between ring
members. [figure]
(1) Note. See section II, Glossary, for the definition
"including hydrogenated".
Subclass:
379
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the oxazole ring as one of the
cyclos:
This subclass is indented under subclass 378. Subject matter
wherein the 1,2-oxazole ring is a cyclo of a polycyclo ring
system.
Subclass:
380
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly to ring carbon of the
oxazole ring:
This subclass is indented under subclass 378. Subject matter
wherein chalcogen or nitrogen is bonded directly to ring
carbon of the 1,2-oxazole ring.
Subclass:
381
![[Patents]](../gifs/ps.gif)
Tetrazoles (including hydrogenated):
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring consists of four ring
nitrogens and one ring carbon and may have double bond
between ring members.
Subclass:
382
![[Patents]](../gifs/ps.gif)
Additional chalcogen containing hetero ring:
This subclass is indented under subclass 381. Subject matter
which contains an additional chalcogen containing hetero
ring.
Subclass:
383
![[Patents]](../gifs/ps.gif)
1,2,4-triazoles (including hydrogenated):
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is 1,2,4-triazole
having the following structure, illustrated below, or
hydrogenated form thereof. [figure] [caption]or [figure]
Subclass:
384
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to the triazole ring:
This subclass is indented under subclass 383. Subject matter
wherein chalcogen is directly bonded to the 1,2,4-triazole.
Subclass:
385
![[Patents]](../gifs/ps.gif)
1,3-diazoles:
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is a 1,3-diazole ring
which includes the following basic ring structure,
illustrated below, and may contain a double bond between ring
members. [figure]
Subclass:
386
![[Patents]](../gifs/ps.gif)
Divalent chalcogen or acyclic nitrogen double bonded directly
to ring carbon of the diazole ring, or tautomeric
equivalent:
This subclass is indented under subclass 385. Subject matter
wherein a ring carbon of the 1,3-diazole ring is bonded
directly by a double bond to divalent chalcogen or acyclic
nitrogen, or to a group which may tautomerize thereto (e.g.,
hydroxyl, sulfhydryl, acyclic amino, etc.).
(1) Note. (A) all 1,3-diazoles having the following
structure, as shown in the first illustration, are classified
in this and indented subclasses; (B) the aminoimidazole, for
example, as shown in the second illustration below, is
included in this subclass though its imino tautomer, as shown
in the third illustration below, may not be present in
significant amounts; (C) salts in which the labile hydrogen
of, for example, an hydroxy, sulfhydryl or amino tautomer is
replaced with a metal or amine salt are classified here.
[figure] [caption]X is chalcogen or NR; A is N or CR'; B is
the remaining ring members of the 1,3-diazole; R is H or a
substituent; R' is H or a substituent [figure] [figure]
Subclass:
387
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the diazole ring as one of the
cyclos:
This subclass is indented under subclass 386. Subject matter
wherein the 1,3-diazole ring is one of the cyclos of a
polycyclo ring system.
Subclass:
388
![[Patents]](../gifs/ps.gif)
Nitrogen double bonded directly at 2-position of the diazole
ring, or tautomeric equivalent:
This subclass is indented under subclass 387. Subject matter
wherein an acyclic nitrogen is double bonded directly to the
ring carbon between two ring nitrogens of the 1,3-diazole
ring, or the amino tautomeric equivalent, e.g., [figure]
[figure] [caption], etc.
Subclass:
389
![[Patents]](../gifs/ps.gif)
Divalent chalcogen or acyclic nitrogen double bonded directly
at both 2- and 4-positions, or tautomeric equivalent (e.g.,
hydantoin, etc.):
This subclass is indented under subclass 386. Subject matter
wherein the ring carbons at the 2- and 4-positions of the
1,3-diazole ring are each bonded directly by a double bond to
divalent chalcogen or acyclic nitrogen, or to a group which
may tautomerize thereto (e.g., hydroxyl, sulfhydryl, acyclic
amino, etc.).
Subclass:
390
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly at 1-, 3-, or
5-position by nonionic bonding:
This subclass is indented under subclass 389. Subject matter
wherein chalcogen or nitrogen is bonded directly to a ring
nitrogen, or to the ring carbon at 5-position of the
1,3-diazole ring by nonionic bonding.
Subclass:
391
![[Patents]](../gifs/ps.gif)
Benzene ring bonded directly to the diazole ring by nonionic
bonding:
This subclass is indented under subclass 389. Subject matter
wherein a benzene ring is bonded directly to 1,3-diazole ring
by nonionic bonding.
Subclass:
392
![[Patents]](../gifs/ps.gif)
Divalent chalcogen or acyclic nitrogen double bonded directly
at 2-position, or tautomeric equivalent:
This subclass is indented under subclass 386. Subject matter
wherein the ring carbon between the two ring nitrogens of the
1,3-diazole ring is bonded directly by a double bond to
divalent chalcogen or acyclic nitrogen, or to a group which
may tautomerize thereto (e.g., hydroxyl, sulfhydryl, acyclic
amino, etc.).
Subclass:
393
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the diazole ring as one of the
cyclos:
This subclass is indented under subclass 385. Subject matter
wherein the 1,3-diazole ring is one of the cyclos of a
polycyclo ring system.
Subclass:
394
![[Patents]](../gifs/ps.gif)
Benzo fused at 4,5-positions of the diazole ring:
This subclass is indented under subclass 393. Subject matter
wherein the polyclo ring system contains a benzo ring which
shares the carbons at 4- and 5-positions of the 1,3-diazole
ring, e.g., benzimidazoles, etc.
Subclass:
395
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly at 1-,2-, or 3-position
of the diazole ring by nonionic bonding:
This subclass is indented under subclass 394. Subject matter
wherein chalcogen or nitrogen is bonded directly to a ring
nitrogen or 2-carbon of the benzo fused 1,3-diazole ring by
nonionic bonding.
Subclass:
396
![[Patents]](../gifs/ps.gif)
Imidazoles:
This subclass is indented under subclass 385. Subject matter
wherein the 1,3-diazole ring is imidazole which contains two
double bonds between the ring members.
Subclass:
397
![[Patents]](../gifs/ps.gif)
Additional hetero ring:
This subclass is indented under subclass 396. Subject matter
which contains an additional hetero ring, e.g., [figure]
[figure] [caption], etc.
Subclass:
398
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly to the imidazole ring
by nonionic bonding:
This subclass is indented under subclass 396. Subject matter
wherein chalcogen or nitrogen is bonded directly to the
imidazole ring by nonionic bonding.
Subclass:
399
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded indirectly to the imidazole ring
by nonionic bonding:
This subclass is indented under subclass 396. Subject matter
wherein chalcogen or nitrogen is bonded indirectly to the
imidazole ring by nonionic bonding.
Subclass:
400
![[Patents]](../gifs/ps.gif)
At imidazole ring carbon:
This subclass is indented under subclass 399. Subject matter
wherein the chalcogen or nitrogen is bonded indirectly to a
ring carbon of the imidazole ring and not through any of the
hetero atoms.
Subclass:
401
![[Patents]](../gifs/ps.gif)
2-imidazolines:
This subclass is indented under subclass 385. Subject matter
wherein the 1,3-diazole ring contains one double bond between
2-carbon and 3-nitrogen.
Subclass:
402
![[Patents]](../gifs/ps.gif)
Additional hetero ring:
This subclass is indented under subclass 401. Subject matter
which contains an additional hetero ring, e.g., [figure]
[figure]
Subclass:
403
![[Patents]](../gifs/ps.gif)
1,2-diazoles:
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring is a 1,2-diazole ring
which includes the following basic ring structure, as
illustrated below, and may contain a double bond between ring
members. [figure]
Subclass:
404
![[Patents]](../gifs/ps.gif)
Divalent chalcogen or acyclic nitrogen double bonded directly
to ring carbon of the diazole ring, or tautomeric
equivalent:
This subclass is indented under subclass 403. Subject matter
wherein a ring carbon of the 1,2-diazole ring is bonded
directly by a double bond to divalent chalcogen or acyclic
nitrogen, or to a group which may tautomerize thereto (e.g.,
hydroxyl, sulfhydryl, acyclic amino, etc.).
(1) Note. (A) all 1,2-diazoles having the following
structure, shown in the first illustration, are classified in
this and indented subclasses; (B) the hydroxy pyrazole, for
example, as shown in the second illustration below, is
included in this subclass though its oxo tautomer, as shown
in the third illustration below, may not be present in
significant amounts; (C) Salts in which the labile hydrogen
of, for example, an hydroxy, sulfhydryl or amino tautomer is
replaced with a metal ion or amine salt are classified here.
[figure] [caption]X is chalcogen or NR; A is N or CR'; B is
the remaining ring members of the 1,2-diazole; R is H or a
substituent; R' is H or a substituent [figure] [figure]
Subclass:
405
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the diazole ring as one of the
cyclos:
This subclass is indented under subclass 404. Subject matter
wherein the 1,2-diazole ring is one of the cyclos of a
polycyclo ring system.
Subclass:
406
![[Patents]](../gifs/ps.gif)
Pyrazoles:
This subclass is indented under subclass 403. Subject matter
wherein the 1,2-diazole ring is pyrazole which contains two
double bonds between ring members.
Subclass:
407
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly to the pyrazole ring by
nonionic bonding:
This subclass is indented under subclass 406. Subject matter
wherein chalcogen or nitrogen is bonded directly to the
pyrazole ring by nonionic bonding.
Subclass:
408
![[Patents]](../gifs/ps.gif)
The five-membered hetero ring consists of one nitrogen and
four carbons:
This subclass is indented under subclass 359. Subject matter
wherein the five-membered hetero ring consists of one
nitrogen and four carbon atoms, e.g., pyrrolidine, etc.
Subclass:
409
![[Patents]](../gifs/ps.gif)
Spiro ring system:
This subclass is indented under subclass 408. Subject matter
which contains a spiro ring system, e.g., [figure] [caption],
etc.
(1) Note. See section II, Glossary, for the definition of
"spiro ring system".
Subclass:
410
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the five-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 408. Subject matter
wherein the five-membered hetero ring is one of the cyclos of
a polycyclo ring system.
Subclass:
411
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the five-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 410. Subject matter
wherein the polycyclo ring system consists of exactly three
cyclos, e.g., [figure] [figure] [caption], etc.
Subclass:
412
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the five-membered hetero ring as
one of the cyclos:
This subclass is indented under subclass 410. Subject matter
wherein the polycyclo ring system consists of exactly two
cyclos, e.g., [figure] [caption], etc.
Subclass:
413
![[Patents]](../gifs/ps.gif)
Ring nitrogen is shared by the cyclos of the bicyclo ring
system:
This subclass is indented under subclass 412. Subject matter
wherein the ring nitrogen of the five-membered hetero ring is
additionally a ring member of the other cyclo of the bicyclo
ring system, e.g.,
Subclass:
414
![[Patents]](../gifs/ps.gif)
Additional hetero ring which is not part of the bicyclo ring
system:
This subclass is indented under subclass 412. Subject matter
which contains an additional hetero ring, e.g., [figure]
[caption], etc.
Subclass:
415
![[Patents]](../gifs/ps.gif)
The bicyclo ring system consists of the five-membered hetero
ring and a benzene ring (e.g., indole, etc.):
This subclass is indented under subclass 412. Subject matter
wherein the five-membered hetero ring and a benzene ring are
the cyclos of the bicyclo ring system, e.g., indole,
indoline, etc.
Subclass:
416
![[Patents]](../gifs/ps.gif)
The ring nitrogen is bonded directly to nonshared ring
carbons of the five-membered hetero ring (e.g., isoindole,
etc.):
This subclass is indented under subclass 415. Subject matter
wherein the ring nitrogen is bonded directly to the two
nonshared ring carbons of the five-membered hetero ring,
e.g., [figure] [figure] [caption], etc.
Subclass:
417
![[Patents]](../gifs/ps.gif)
Plural chalcogens bonded directly to ring carbons of the
five-membered hetero ring (e.g., phthalimide, etc.):
This subclass is indented under subclass 416. Subject matter
wherein at least two chalcogens are bonded directly to ring
carbons of the five-membered hetero ring, e.g., phthalimide,
etc.
Subclass:
418
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the five-membered
hetero ring:
This subclass is indented under subclass 415. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
five-membered.
Subclass:
419
![[Patents]](../gifs/ps.gif)
C=X bonded directly or indirectly by an acyclic carbon or
carbon chain to ring carbon of the five-membered hetero ring
(e.g., trytophan, etc.) (X is chalcogen):
This subclass is indented under subclass 415. Subject matter
wherein a C=X group (X is Chalcogen) is bonded directly or
indirectly to a ring carbon of the five-membered hetero ring
by an acyclic carbon or carbon chain, e.g., [figure]
[caption], etc.
Subclass:
420
![[Patents]](../gifs/ps.gif)
Indomethacin, per se, or ester thereof:
This subclass is indented under subclass 419. Subject matter
wherein the compound is indomethacin, i.e., as illustrated
below, or ester of the carboxyl group thereof. [figure]
Subclass:
421
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the five-membered
hetero ring (e.g., adrenochrome, etc.):
This subclass is indented under subclass 412. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
five-membered hetero ring, e.g., [figure] [caption], etc.
Subclass:
422
![[Patents]](../gifs/ps.gif)
Additional hetero ring:
This subclass is indented under subclass 408. Subject matter
which contains an additional hetero ring, e.g., [figure]
[figure] [caption], etc.
Subclass:
423
![[Patents]](../gifs/ps.gif)
C=X bonded directly to the five-membered hetero ring by
nonionic bonding (X is chalcogen):
This subclass is indented under subclass 408. Subject matter
wherein C=X (X is chalcogen) is bonded directly to the
five-membered hetero ring by nonionic bonding.
Subclass:
424
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to the five-membered hetero ring by
nonionic bonding:
This subclass is indented under subclass 408. Subject matter
wherein chalcogen is bonded directly to the five-membered
hetero ring by nonionic bonding.
Subclass:
425
![[Patents]](../gifs/ps.gif)
Plural chalcogens bonded directly to the five-membered hetero
ring by nonionic bonding:
This subclass is indented under subclass 424. Subject matter
wherein at least two chalcogens are bonded directly to the
five-membered hetero ring by nonionic bonding.
Subclass:
426
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to the five-membered hetero ring by
nonionic bonding:
This subclass is indented under subclass 408. Subject matter
wherein nitrogen is bonded directly to the five-membered
hetero ring by nonionic bonding.
Subclass:
427
![[Patents]](../gifs/ps.gif)
Two double bonds between ring members of the five-membered
hetero ring (e.g., pyrrole, etc.):
This subclass is indented under subclass 408. Subject matter
which contains two double bonds between ring members of the
five-membered hetero ring, e.g., pyrrole, etc.
Subclass:
428
![[Patents]](../gifs/ps.gif)
Chalcogen bonded indirectly to the five-membered hetero ring
by acyclic nonionic bonding:
This subclass is indented under subclass 408. Subject matter
wherein chalcogen is bonded indirectly to the five-membered
hetero ring by acyclic nonionic bonding, e.g., [figure]
[figure] [caption], etc.
Subclass:
429
![[Patents]](../gifs/ps.gif)
Carbocyclic ring bonded directly to the five-membered hetero
ring:
This subclass is indented under subclass 408. Subject matter
wherein a carbocyclic ring is bonded directly to the
five-membered hetero ring.
Subclass:
430
![[Patents]](../gifs/ps.gif)
Sulfur containing hetero ring:
This subclass is indented under subclass 183. Subject matter
wherein the hetero ring has sulfur as a ring hetero atom.
(1) Note. Inner sulfonium salts, even when represented in
cyclic form are excluded herefrom.
Subclass:
431
![[Patents]](../gifs/ps.gif)
The hetero ring has at least seven members:
This subclass is indented under subclass 430. Subject matter
wherein the hetero ring has at least seven members.
Subclass:
432
![[Patents]](../gifs/ps.gif)
The hetero ring is six-membered:
This subclass is indented under subclass 430. Subject matter
wherein the hetero ring is six-membered.
Subclass:
433
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the hetero ring:
This subclass is indented under subclass 432. Subject matter
wherein the hetero ring contains at least one ring hetero
atom in addition to the ring sulfur.
Subclass:
434
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 433. Subject matter
wherein the hetero ring is one of the cyclos of a polycyclo
ring system.
Subclass:
435
![[Patents]](../gifs/ps.gif)
Three or more ring hetero atoms in the hetero ring:
This subclass is indented under subclass 433. Subject matter
wherein the six-membered hetero ring contains at least two
ring hetero atoms in addition to the ring sulfur.
Subclass:
436
![[Patents]](../gifs/ps.gif)
Two ring sulfurs in the hetero ring:
This subclass is indented under subclass 433. Subject matter
wherein the six-membered hetero ring contains at least two
ring hetero atoms in addition to the ring sulfur.
Subclass:
437
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 432. Subject matter
wherein the hetero ring is one of the cyclos of a polycyclo
ring system consisting of exactly three cyclos.
Subclass:
438
![[Patents]](../gifs/ps.gif)
The hetero ring is five-membered:
This subclass is indented under subclass 430. Subject matter
wherein the hetero ring is five-membered.
Subclass:
439
![[Patents]](../gifs/ps.gif)
Plural hetero atoms in the hetero ring:
This subclass is indented under subclass 438. Subject matter
wherein the hetero ring has at least one ring hetero atom in
addition to the ring sulfur.
Subclass:
440
![[Patents]](../gifs/ps.gif)
Only two ring sulfurs in the hetero ring:
This subclass is indented under subclass 439. Subject matter
wherein the hetero ring contains exactly two ring sulfurs as
the only hetero atoms present.
Subclass:
441
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the hetero ring:
This subclass is indented under subclass 440. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
hetero ring.
Subclass:
442
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to the hetero ring by nonionic
bonding:
This subclass is indented under subclass 440. Subject matter
wherein nitrogen is bonded directly to the hetero ring by
nonionic bonding.
Subclass:
443
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 438. Subject matter
wherein the five-membered sulfur containing hetero ring is
one of the cyclos of a polycyclo ring system.
Subclass:
444
![[Patents]](../gifs/ps.gif)
Additional hetero ring:
This subclass is indented under subclass 438. Subject matter
wherein an additional hetero ring is present.
(1) Note. Examples of compounds Provided for herein are:
[figure] [figure] [caption], etc.
Subclass:
445
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the hetero ring:
This subclass is indented under subclass 438. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
hetero ring.
Subclass:
446
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring sulfur by nonionic
bonding:
This subclass is indented under subclass 438. Subject matter
wherein chalcogen is bonded directly to ring sulfur of the
hetero ring.
Subclass:
447
![[Patents]](../gifs/ps.gif)
Nitrogen bonded directly to the hetero ring:
This subclass is indented under subclass 438. Subject matter
wherein nitrogen is bonded directly to the hetero ring.
(1) Note. An example of a compound within this definition:
[figure]
Subclass:
448
![[Patents]](../gifs/ps.gif)
C=X bonded directly to the hetero ring (X is chalcogen):
This subclass is indented under subclass 438. Subject matter
wherein C=X (X is chalcogen) is bonded directly to the hetero
ring.
Subclass:
449
![[Patents]](../gifs/ps.gif)
Oxygen containing hetero ring:
This subclass is indented under subclass 183. Subject matter
wherein the hetero ring contains a ring oxygen.
Subclass:
450
![[Patents]](../gifs/ps.gif)
The hetero ring has at least seven members:
This subclass is indented under subclass 449. Subject matter
wherein the hetero ring has seven or more members.
Subclass:
451
![[Patents]](../gifs/ps.gif)
The hetero ring is six-membered:
This subclass is indented under subclass 449. Subject matter
wherein the hetero ring is six-membered.
Subclass:
452
![[Patents]](../gifs/ps.gif)
Plural ring oxygens in the hetero ring:
This subclass is indented under subclass 451. Subject matter
wherein the six-membered hetero ring contains at least two
ring oxygens.
Subclass:
453
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 451. Subject matter
wherein the six-membered hetero ring is one of the cyclos of
a polycyclo ring system.
Subclass:
454
![[Patents]](../gifs/ps.gif)
Tricyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 453. Subject matter
wherein the polycyclo ring system consists of exactly three
cyclos.
Subclass:
455
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the hetero ring:
This subclass is indented under subclass 454. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
hetero ring.
Subclass:
456
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the hetero ring as one of the
cyclos (e.g., chromones, etc.):
This subclass is indented under subclass 453. Subject matter
wherein the polycyclo ring system consists of exactly two
cyclos.
Subclass:
457
![[Patents]](../gifs/ps.gif)
Coumarins (including hydrogenated):
This subclass is indented under subclass 456. Subject matter
wherein the bicyclo ring system has the following structure,
as illustrated below, or hydrogenated form thereof. [figure]
Subclass:
458
![[Patents]](../gifs/ps.gif)
Tocopherols (e.g., vitamin E, etc.):
This subclass is indented under subclass 456. Subject matter
wherein the bicyclo ring system includes the following
structure, in the first illustration below, or ether, ester
of the hydroxyl group thereof, e.g., as shown in the second
illustration below. [figure] [figure] [caption], etc.
(1) Note. The several tocopherols differ by methyl
substitution on the benzo ring.
Subclass:
459
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 451. Subject matter
which contains nitrogen.
Subclass:
460
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to ring carbon of the hetero ring:
This subclass is indented under subclass 451. Subject matter
wherein chalcogen is bonded directly to ring carbon of the
hetero ring.
Subclass:
461
![[Patents]](../gifs/ps.gif)
The hetero ring is five-membered:
This subclass is indented under subclass 449. Subject matter
wherein the hetero ring is five-membered.
Subclass:
462
![[Patents]](../gifs/ps.gif)
Spiro ring system:
This subclass is indented under subclass 461. Subject matter
which contains a spiro ring system, e.g., [figure] [figure]
[caption], etc.
(1) Note. See section IV, Glossary, for the definition of
"spiro ring system."
Subclass:
463
![[Patents]](../gifs/ps.gif)
Plural ring oxygens in the hetero ring:
This subclass is indented under subclass 461. Subject matter
wherein the five-membered hetero ring contains at least two
ring oxygens.
Subclass:
464
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the hetero ring as one of the
cyclos (e.g., methylenedioxyphenyl group, etc.):
This subclass is indented under subclass 463. Subject matter
wherein the hetero ring is one of the cyclos of a bicyclo
ring system, e.g., [figure] [caption], etc.
Subclass:
465
![[Patents]](../gifs/ps.gif)
The hetero ring is substituted:
This subclass is indented under subclass 464. Subject matter
wherein the hetero ring contains substituents other than
hydrogen.
Subclass:
466
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 464. Subject matter
which contains nitrogen, e.g., [figure] [caption], etc.
Subclass:
467
![[Patents]](../gifs/ps.gif)
Only two ring oxygens in the hetero ring which is not a
polycyclo ring system (e.g., dioxolane, etc.):
This subclass is indented under subclass 463. Subject matter
wherein the hetero ring contains only two oxygens as ring
hetero atoms and is not a cyclo of a polycyclo ring system.
Subclass:
468
![[Patents]](../gifs/ps.gif)
Polycyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 461. Subject matter
wherein the five-membered hetero ring is one of the cyclos of
a polycyclo ring system.
Subclass:
469
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having the hetero ring as one of the
cyclos:
This subclass is indented under subclass 468. Subject matter
wherein the polycyclo ring system consists of exactly two
cyclos.
Subclass:
470
![[Patents]](../gifs/ps.gif)
Chalcogen or nitrogen bonded directly to the hetero ring:
This subclass is indented under subclass 469. Subject matter
wherein chalcogen or nitrogen is bonded directly to the
hetero ring.
Subclass:
471
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 461. Subject matter
which contains nitrogen.
Subclass:
472
![[Patents]](../gifs/ps.gif)
The nitrogen bonded directly to the hetero ring:
This subclass is indented under subclass 471. Subject matter
wherein the nitrogen is bonded directly to the hetero ring.
Subclass:
473
![[Patents]](../gifs/ps.gif)
Chalcogen bonded directly to the hetero ring:
This subclass is indented under subclass 461. Subject matter
wherein chalcogen is bonded directly to the hetero ring.
Subclass:
474
![[Patents]](../gifs/ps.gif)
Ascorbic acid or derivative (e.g., vitamin c, etc.):
This subclass is indented under subclass 473. Subject matter
which has the following structure, as illustrated below, or
derivative thereof. [figure]
(1) Note. A derivative of ascorbic acid includes the
replacement of hydroxyl hydrogen with acyl, alkyl or metal to
give the ester, ether or alcoholate of a metal.
Subclass:
475
![[Patents]](../gifs/ps.gif)
The hetero ring is three-membered:
This subclass is indented under subclass 449. Subject matter
wherein the oxygen containing hetero ring is three-membered.
Subclass:
476
![[Patents]](../gifs/ps.gif)
N-C (=X) X containing (X is chalcogen) DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the DOAI contains the grouping NX wherein X is
chalcogen, e.g., H[subscrpt]2[end subscrpt]NOH etc.
Subclass:
477
![[Patents]](../gifs/ps.gif)
N-C (=X)-X-N containing:
This subclass is indented under subclass 476. Subject matter
wherein the active ingredient contains the grouping NXN
wherein X is chalcogen, e.g., R[subscrpt]2[end
subscrpt]-NS-NH[subscrpt]2[end subscrpt], etc.
Subclass:
478
![[Patents]](../gifs/ps.gif)
N-C (=X)-X-C containing:
This subclass is indented under subclass 476. Subject matter
in which the active ingredient is an ester of carbamic acid,
i.e., H-XN (X is chalcogen) and which contains the NX-C
group, e.g., [figure] [caption], etc.
Subclass:
479
![[Patents]](../gifs/ps.gif)
With an additional active ingredient:
This subclass is indented under subclass 478. Subject matter
which contains a compound having the grouping, as shown
below, and an additional organic active ingredient.
[figure]
(1) Note. Synergistic and potentiating agents are
considered active ingredients.
Subclass:
480
![[Patents]](../gifs/ps.gif)
Polycyclo ring system attached by nonionic bonding:
This subclass is indented under subclass 478. Subject matter
wherein the compound contains a polycyclo ring system, e.g.,
[figure] [caption], etc.
(1) Note. Compounds wherein the polycyclo system is
ionically bonded to the moiety containing the grouping, as
shown below, are excluded from this subclass. [figure]
Subclass:
481
![[Patents]](../gifs/ps.gif)
Naphthyl ring system:
This subclass is indented under subclass 480. Subject matter
wherein the compound contains a naphthyl ring system, e.g.,
[figure] [caption], etc.
Subclass:
482
![[Patents]](../gifs/ps.gif)
N-C(=X)-N, N-C (=N)N, N-N, nitrogen directly bonded to oxygen
by nonionic bonding or cyano containing:
This subclass is indented under subclass 478. Subject matter
which contains the grouping NN (e.g., ureido);NN, (e.g.,
guanido); N-N (e.g., hydrazo, etc.), cyano or a nitrogen
bonded directly to oxygen by nonionic bonding.
(1) Note. This subclass contains, for example, [figure]
[caption], etc.
Subclass:
483
![[Patents]](../gifs/ps.gif)
Plural N-C(=X)-X groups:
This subclass is indented under subclass 478. Subject matter
wherein the organic ingredient contains plural NX groups,
e.g., [figure] [caption], etc.
Subclass:
484
![[Patents]](../gifs/ps.gif)
Ring in acid moiety:
This subclass is indented under subclass 478. Subject matter
wherein the organic active ingredient has a ring in the acid
moiety, e.g., [figure] [caption], etc.
Subclass:
485
![[Patents]](../gifs/ps.gif)
The ring is a benzene ring:
This subclass is indented under subclass 484. Subject matter
wherein the ring is a benzene ring.
(1) Note. This subclass contains, e.g., [figure] [caption],
etc.
Subclass:
486
![[Patents]](../gifs/ps.gif)
Phenoxy in acid moiety:
This subclass is indented under subclass 485. Subject matter
wherein the benzene ring is a part of a phenoxy group, e.g.,
[figure] [caption], etc.
Subclass:
487
![[Patents]](../gifs/ps.gif)
The benzene ring attached to nitrogen through an acyclic
carbon or carbon chain:
This subclass is indented under subclass 485. Subject matter
wherein the benzene ring is attached to the nitrogen of the
NXC group through an acyclic carbon or carbon chain.
(1) Note. This subclass contains, e.g., [figure] [caption],
etc.
Subclass:
488
![[Patents]](../gifs/ps.gif)
Ring in alcohol moiety:
This subclass is indented under subclass 485. Subject matter
wherein the organic active ingredient also contains a ring in
the alcohol moiety.
(1) Note. This subclass contains, e.g., [figure] [caption],
etc.
Subclass:
489
![[Patents]](../gifs/ps.gif)
Ring in alcohol moiety:
This subclass is indented under subclass 478. Subject matter
wherein the active ingredient contains a ring in the alcohol
moiety.
(1) Note. This subclass contains, e.g., [figure] [caption],
etc.
Subclass:
490
![[Patents]](../gifs/ps.gif)
Ring attached directly to oxygen of N-C(=O)-O:
This subclass is indented under subclass 489. Subject matter
wherein the ring is directly attached to the oxygen of the
NO.
(1) Note. This subclass contains, e.g., [figure] [caption],
etc.
Subclass:
491
![[Patents]](../gifs/ps.gif)
With an additional active ingredient:
This subclass is indented under subclass 476. Subject matter
which contains a compound having the grouping NX and an
additional organic active ingredient.
(1) Note. Synergistic and potentiating agents are
considered active ingredients.
Subclass:
492
![[Patents]](../gifs/ps.gif)
Heavy metal containing DOAI:
This subclass is indented under subclass 1. Subject matter
in which the DOAI contains a heavy metal, i.e., a metal whose
specific gravity is greater than 4.
(1) Note. Many patents in this and indented subclasses are
drawn to compositions containing heavy metal salts of organic
compounds.
Subclass:
493
![[Patents]](../gifs/ps.gif)
Tin:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is tin.
Subclass:
494
![[Patents]](../gifs/ps.gif)
Zinc:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is zinc.
Subclass:
495
![[Patents]](../gifs/ps.gif)
Gold or silver:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is gold or silver.
Subclass:
496
![[Patents]](../gifs/ps.gif)
Mercury:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is mercury.
Subclass:
497
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 496. Subject matter
in which the heavy metal containing compound also contains a
nitrogen atom.
Subclass:
498
![[Patents]](../gifs/ps.gif)
Lead:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is lead.
Subclass:
499
![[Patents]](../gifs/ps.gif)
Copper:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is copper.
Subclass:
500
![[Patents]](../gifs/ps.gif)
With an additional active ingredient:
This subclass is indented under subclass 499. Subject matter
which contains a compound which contains copper and also an
additional active ingredient.
(1) Note. Synergistic and potentiating agents are
considered active ingredients.
Subclass:
501
![[Patents]](../gifs/ps.gif)
Nickel or cobalt:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is nickel or cobalt.
Subclass:
502
![[Patents]](../gifs/ps.gif)
Iron:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is iron.
Subclass:
503
![[Patents]](../gifs/ps.gif)
Antimony or bismuth:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is antimony or bismuth.
Subclass:
504
![[Patents]](../gifs/ps.gif)
Arsenic:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is arsenic.
Subclass:
505
![[Patents]](../gifs/ps.gif)
Cadmium or chromium:
This subclass is indented under subclass 492. Subject matter
in which the heavy metal is cadmium or chromium.
Subclass:
506
![[Patents]](../gifs/ps.gif)
Ester DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the DOAI is identical in structure with a compound
formed by replacing the hydroxyl of an alcohol or phenol by
an acid radical.
Subclass:
507
![[Patents]](../gifs/ps.gif)
R-C(=X)-N-X-C containing (e.g., hydroxamic acid ester, etc.)
(R is C or H and X is chalcogen):
This subclass is indented under subclass 506. Subject matter
in which the ester contains the following group: RNXC,
wherein R is carbon or hydrogen and X is chalcogen (e.g.,
hydroxamic acid ester, etc.).
(1) Note. This subclass contains for example: [figure]
[figure] [caption], etc.
Subclass:
508
![[Patents]](../gifs/ps.gif)
X-C=N containing (e.g., imidoester, etc.) (X is chalcogen):
This subclass is indented under subclass 506. Subject matter
in which the ester contains the following group: X-C=N
wherein X is chalcogen (e.g., imidoester, etc.).
(1) Note. This subclass contains for example: [figure]
[figure] [caption], etc.
Subclass:
509
![[Patents]](../gifs/ps.gif)
(O=)N(=O)-O-C containing (e.g., nitrate ester, etc.):
This subclass is indented under subclass 506. Subject matter
wherein the ester contains the group (O=)N(=O)-O-C.
(1) Note. This subclass contains for example: [figure]
[caption], etc.
Subclass:
510
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 506. Subject matter
wherein the ester contains a polycyclo ring system in either
the alcohol or acid portion of the molecule.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
511
![[Patents]](../gifs/ps.gif)
Two of the cyclos share at least three ring members (i.e.,
bridged):
This subclass is indented under subclass 510. Subject matter
wherein the ester contains at least one bridged ring system
in either the alcohol or acid portion of the molecule.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
512
![[Patents]](../gifs/ps.gif)
X-C(=X)-X containing (e.g., carbonic acid ester, thiocarbonic
acid ester, etc.) (X is chalcogen):
This subclass is indented under subclass 506. Subject matter
wherein the ester contains the group XX, wherein X is
chalcogen.
(1) Note. This subclass contains, for example: [figure]
[figure] [figure] [caption], etc.
Subclass:
513
![[Patents]](../gifs/ps.gif)
C-C(=X)-X-C containing (X is chalcogen and at least one X is
other than oxygen):
This subclass is indented under subclass 506. Subject matter
wherein the ester contains the group group CXC wherein X is
chalcogen and at least one is other than oxygen.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
514
![[Patents]](../gifs/ps.gif)
Carbon bonded to -NCX (e.g., cyanate, thiocyanate or
isothiocyanate, etc.) (X is chalcogen):
This subclass is indented under subclass 506. Subject matter
wherein the organic action ingredient contains a carbon which
is directly bonded to -NCX or -XCN.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
515
![[Patents]](../gifs/ps.gif)
With an additional active ingredient:
This subclass is indented under subclass 514. Subject matter
wherein the organic active ingredient contains a compound
having the group -CNX or -XCN and an additional organic
active ingredient.
(1) Note. Synergistic and potentiating agents are
considered active ingredients.
(2) Note. The starting solid polymer may be subjected to a
number of aftertreating steps the sequence or numbers of
which will not affect classification. The important criteria
is that every reaction be considered proceeding from the
starting solid polymer to the final product. This is
consistent with the classification rules set out in the Class
520 Series.
Subclass:
516
![[Patents]](../gifs/ps.gif)
Containing plural -NCX or -XCN groups or a cyano:
This subclass is indented under subclass 514. Subject matter
in which the organic active ingredient contains plural -NCX
or -XCN groups or a separate cyano group which is not a part
of the -NCX or -XCN group.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
517
![[Patents]](../gifs/ps.gif)
S-X-C containing (e.g., sulfates, etc.) (S is chalcogen):
This subclass is indented under subclass 506. Subject matter
wherein the ester is derived from a sulfur oxygen acid
function of the formula RSOH, RXH, plus see the
illustrations below: [figure] [figure] [caption] or
[figure]
(1) Note. This subclass contains, for example: [figure]
[figure] [figure] [caption], etc.
Subclass:
518
![[Patents]](../gifs/ps.gif)
S of S-X-C attached directly to a benzene ring:
This subclass is indented under subclass 517. Subject matter
wherein the sulfur atom of the S-X-C is directly attached to
a benzene ring.
(1) Note. This subclass contains for example: [figure]
[caption], etc.
Subclass:
519
![[Patents]](../gifs/ps.gif)
Cyano or isocyano bonded directly to carbon:
This subclass is indented under subclass 506. Subject matter
wherein the ester is the -C b N (cyano) or the -[supscrpt]+
[end supscrpt]b C (isocyano also written as -N = C group)
attached to a carbon.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
520
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 303. Subject matter
in which the cyano or isocyano containing compound also
contains a benzene ring.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
521
![[Patents]](../gifs/ps.gif)
C=O other than as ketone or aldehyde:
This subclass is indented under subclass 520. Subject matter
in which the cyano or isocyano and benzene ring containing
compound also contains a C=D (carbonyl) other than as a
ketone or aldehyde.
(1) Note. This subclass contains, for examples: [figure]
[caption], etc.
Subclass:
522
![[Patents]](../gifs/ps.gif)
The cyano is bonded directly to a benzene ring:
This subclass is indented under subclass 521. Subject matter
wherein the cyano group is bonded directly to a benzene
ring.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
523
![[Patents]](../gifs/ps.gif)
Additional nitrogen other than cyano:
This subclass is indented under subclass 520. Subject matter
wherein the cyano and benzene containing compound also
contains an additional nitrogen other than as in a cyano or
isocyano grouping.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
524
![[Patents]](../gifs/ps.gif)
The cyano is bonded directly to a benzene ring:
This subclass is indented under subclass 523. Subject matter
wherein a cyano group is bonded directly to a benzene ring.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
525
![[Patents]](../gifs/ps.gif)
Two or more of the cyano groups:
This subclass is indented under subclass 520. Subject matter
wherein the compound contains a benzene ring and at least two
cyano groups.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
526
![[Patents]](../gifs/ps.gif)
Acyclic:
This subclass is indented under subclass 519. Subject matter
wherein the cyano containing compound is acyclic.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
527
![[Patents]](../gifs/ps.gif)
C=O other than as ketone or aldehyde:
This subclass is indented under subclass 526. Subject matter
wherein the acyclic cyano containing compound contains a C=O
(carbonyl) other than as ketone or aldehyde.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
528
![[Patents]](../gifs/ps.gif)
C(=O)N containing:
This subclass is indented under subclass 527. Subject matter
wherein the carbonyl group is present in the form of a
carboxamide grouping, [figure]
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
529
![[Patents]](../gifs/ps.gif)
Z-C(=O)-O-Y wherein Z is hydrogen or an organic radical
bonded to the C(=O) by a carbon and Y is an organic radical
bonded to the oxygen by a carbon:
This subclass is indented under subclass 506. Subject matter
wherein the ester is derived from a carboxylic acid of the
formula ZO-Y wherein the Z and Y are organic radicals
directly bonded by carbon atoms or Z is a hydrogen atom.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
(2) Note. A compound which contains plural radicals, is
proper for the subclass hereunder if the Z (or Y) of any one
of the radicals meets the requirements for Z (or Y) in the
subclass.
Subclass:
530
![[Patents]](../gifs/ps.gif)
Z contains a cyclopentyl or cyclopentene ring:
This subclass is indented under subclass 529. Subject matter
wherein the Z is or contains a cyclopentyl or cyclopentene
moiety.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
531
![[Patents]](../gifs/ps.gif)
Z contains a cyclopropyl or cyclopropene ring:
This subclass is indented under subclass 529. Subject matter
wherein Z is or contains a cyclopropyl or cyclopropene
moiety.
(1) Note. This subclass contains for example: [figure]
[figure] [caption], etc.
(2) Note. A Compound which contains plural ZO-Y radicals is
proper for the subclasses hereunder if the A (or Y) of any of
the radicals meets the requirements for Z (or Y) in the
subclass.
Subclass:
532
![[Patents]](../gifs/ps.gif)
Z-C(=O)-O-Y, wherein Z contains a benzene ring:
This subclass is indented under subclass 529. Subject matter
wherein Z is or contains a benzene ring.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
533
![[Patents]](../gifs/ps.gif)
Compound contains two or more C(=O)O groups indirectly bonded
together by only covalent bonds:
This subclass is indented under subclass 532. Subject matter
wherein the ester contains two of more O- groups.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
(2) Note. Exclude if formed because of ionic bonding, e.g.,
[figure] [caption], etc.
Subclass:
534
![[Patents]](../gifs/ps.gif)
Z or Y radical contains a nitrogen atom:
This subclass is indented under subclass 532. Subject matter
wherein the Z or Y radical contains a nitrogen atom.
(1) Note. The subclass contains, for example: [figure]
[caption], etc.
Subclass:
535
![[Patents]](../gifs/ps.gif)
The nitrogen of the Z radical is directly bonded to a benzene
ring which is directly bonded to the C(=O) group:
This subclass is indented under subclass 534. Subject matter
wherein the nitrogen of the Z radical is directly attached to
a benzene ring which is directly attached to the C=O of the
C(=O) -OY grouping.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
536
![[Patents]](../gifs/ps.gif)
With an agent to enhance topical adsorption or with a
stabilizing agent:
This subclass is indented under subclass 535. Subject matter
wherein the composition includes an agent which acts as a
stabilizer for the active ingredient therein or acts to
enhance the topical absorption thereof.
(1) Note. To be included herein the agent must be disclosed
to have one of said functions.
Subclass:
537
![[Patents]](../gifs/ps.gif)
With an additional active ingredient:
This subclass is indented under subclass 535. Subject matter
wherein an additional active ingredient is present along with
the DOAI.
Subclass:
538
![[Patents]](../gifs/ps.gif)
Nitrogen bonded to carbon in Z moiety:
This subclass is indented under subclass 534. Subject matter
wherein the nitrogen is bonded to a carbon in the Z radical.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
539
![[Patents]](../gifs/ps.gif)
Plural separated benzene rings in Z moiety:
This subclass is indented under subclass 538. Subject matter
wherein the active ingredient contains two or more separate
benzene rings in the Z radical.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
540
![[Patents]](../gifs/ps.gif)
Nitrogen in Y moiety:
This subclass is indented under subclass 538. Subject matter
wherein at least one nitrogen atom is also present in the Y
radical.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
541
![[Patents]](../gifs/ps.gif)
Aldehyde or ketone in Z or Y radical:
This subclass is indented under subclass 538. Subject matter
wherein the active ingredient contains a ketone or aldehyde
grouping in the Z or Y radical.
Subclass:
542
![[Patents]](../gifs/ps.gif)
Z radical contains two or more nitrogen atoms at least one of
which forms a C(=X)N group (X is chalcogen):
This subclass is indented under subclass 538. Subject matter
wherein the Z radical contains two or more nitrogen atoms, at
least one of which is present in the form a C(=X)-N group,
wherein X is chalcogen.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
543
![[Patents]](../gifs/ps.gif)
Z forms a phenoxyl alky or phenoxy alkenyl radical:
This subclass is indented under subclass 532. Subject matter
wherein Z is a substituted or unsubstituted Phenoxy alkyl or
phenoxy alkenyl radical.
(1) Note. This subclass contains, for example, as
illustrated below, wherein an oxyalkyl or oxyalkenyl group is
between the phenyl and carbonyl of the ester function.
[figure] [caption], etc.
Subclass:
544
![[Patents]](../gifs/ps.gif)
C(=O) attached directly through the carbon to a benzene
ring:
This subclass is indented under subclass 532. Subject matter
wherein the benzene ring is attached directly to the carbon
of the C(=O)-OY.
(1) Note. This subclass contains, for example: [figure]
Subclass:
545
![[Patents]](../gifs/ps.gif)
Ketone in Z radical:
This subclass is indented under subclass 532. Subject matter
wherein a ketone grouping is present in the Z moiety.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
546
![[Patents]](../gifs/ps.gif)
ZC(=O)OY, wherein Z is an acyclic radical bonded to the C=O
by a carbon and Y is an organic radical bonded to the oxygen
by a carbon:
This subclass is indented under subclass 529. Subject matter
wherein Z is an acyclic directly bonded to the C+O by a
carbon and Y is an organic radical directly bonded to the
oxygen by a carbon.
(1) Note. This subclass contains, for example:
CH[subscrpt]3[end subscrpt]O-CH[subscrpt]2[end
subscrpt]-CH-C[subscrpt]2[end subscrpt]H[subscrpt]5[end
subscrpt], etc.NO[subscrpt]2[end subscrpt]
Subclass:
547
![[Patents]](../gifs/ps.gif)
Compound contains two of more C(=O)O groups:
This subclass is indented under subclass 546. Subject matter
wherein the active ingredient contains two or more groups.
(1) Note. This subclass contains, for example: [figure]
[caption], etc
Subclass:
548
![[Patents]](../gifs/ps.gif)
Ring in alcohol moiety:
This subclass is indented under subclass 547. Subject matter
wherein the Y moiety contains a carbocyclic ring.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
549
![[Patents]](../gifs/ps.gif)
Z radical contains carbon to carbon unsaturation:
This subclass is indented under subclass 546. Subject matter
wherein the Z radical contains carbon to carbon
unsaturation.
(1) Note. This subclass contains, for example: [figure]
Subclass:
550
![[Patents]](../gifs/ps.gif)
Z radical contains sulfur or halogen:
This subclass is indented under subclass 546. Subject matter
wherein the Z radical contains a sulfur or halogen atom.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
551
![[Patents]](../gifs/ps.gif)
Z radical contains nitrogen:
This subclass is indented under subclass 546. Subject matter
wherein the Z radical contains a nitrogen atom.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
552
![[Patents]](../gifs/ps.gif)
Z contains an unbroken chain of a least seven carbon atoms
bonded directly to the C(=O) group:
This subclass is indented under subclass 546. Subject matter
which contains an ester of a higher fatty acid, i.e., a
monocarboxylic acid containing an unbroken chain of at least
seven acyclic carbon atoms bonded to a carboxylic group.
Subclass:
553
![[Patents]](../gifs/ps.gif)
Radical -XH acid, or anhydride, acid halide or salt thereof
(X is chalcogen) DOAI:
This subclass is indented under subclass 1. Subject matter
which contains a DOAI which has the structure M-A-X-H where A
is sulfur, selenium, tellurium, as illustrated below, wherein
X,Y and Z are Chalcogens, n=1 or 2 and X is not identical to
A, anhydride acid halide or salt thereof, M being any radical
not provided for above. [figure]
(1) Note. Unless otherwise provided for, the salt of an
acid is classified on the basis of the corresponding acid.
(2) Note. This subclass specifically provides for acyclic
anhydrides and acyclic acyl halides.
Subclass:
554
![[Patents]](../gifs/ps.gif)
Amine addition salt of the acid:
This subclass is indented under subclass 553. Subject matter
in which the active ingredient is an addition salt of an
amine and an organic acid.
(1) Note. For the purpose of this and indented subclasses,
amines are compounds identical in constitution with the
derivatives of ammonia (NH[subscrpt]3[end subscrpt]) wherein
the nitrogen atom thereof is bonded to at least one carbon of
an organic radical.
(2) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
555
![[Patents]](../gifs/ps.gif)
Benzene ring in acid moiety:
This subclass is indented under subclass 554. Subject matter
wherein the acid moiety contains a benzene ring.
(1) Note. This subclass contains for example: [figure]
[caption], etc.
Subclass:
556
![[Patents]](../gifs/ps.gif)
Inner quarternary ammonium salt (e.g., betaine, etc.):
This subclass is indented under subclass 553. Subject matter
wherein the active ingredient is an inner quaternary ammonium
salt, as in betaine.
(1) Note. This subclass contains, for example: [figure]
[figure] [caption], etc.
Subclass:
557
![[Patents]](../gifs/ps.gif)
Carboxylic acid, percarboxylic acid, or salt thereof (e.g.,
peracetic acid, etc.):
This subclass is indented under subclass 553. Subject matter
wherein the active ingredient is a carboxylic acid (R-COOH),
or percarboxylic acid (RO-OH) or salt thereof, and wherein R
is hydrogen or an organic radical bonded to the C=O by a
carbon.
Subclass:
558
![[Patents]](../gifs/ps.gif)
Higher fatty acid or salt thereof:
This subclass is indented under subclass 557. Subject matter
wherein the acyl group has an unbroken chain of at least
seven acyclic carbon atoms bonded to the carbon of the
carbonyl group, i.e., higher fatty acids.
Subclass:
559
![[Patents]](../gifs/ps.gif)
Ring containing:
This subclass is indented under subclass 558. Subject matter
wherein the organic active ingredient contains a carbocyclic
ring attached indirectly or directly to the higher fatty acid
chain.
Subclass:
560
![[Patents]](../gifs/ps.gif)
Carbon to carbon unsaturation:
This subclass is indented under subclass 558. Subject matter
wherein the chain of at least seven carbon atoms has carbon
to carbon unsaturation.
Subclass:
561
![[Patents]](../gifs/ps.gif)
Nitrogen other than as nitro or nitroso nonionically bonded:
This subclass is indented under subclass 557. Subject matter
wherein the organic active ingredient contains a nitrogen
atom other than as nitro or nitroso nonionically bonded
thereto.
Subclass:
562
![[Patents]](../gifs/ps.gif)
Sulfur nonionically bonded:
This subclass is indented under subclass 561. Subject matter
wherein the organic active ingredient also contains a sulfur
atom nonionically bonded thereto.
Subclass:
563
![[Patents]](../gifs/ps.gif)
RC)=O)N containing (i.e., carboxamide) (R is C or H):
This subclass is indented under subclass 561. Subject matter
wherein at least one nitrogen is present in a carboxamido
group, i.e., RC(=O)N, wherein R is C or H.
Subclass:
564
![[Patents]](../gifs/ps.gif)
Plural nitrogens nonionically bonded:
This subclass is indented under subclass 561. Subject matter
wherein at least two nitrogen atoms are nonionically bonded
to the active ingredient.
Subclass:
565
![[Patents]](../gifs/ps.gif)
N-N or N=C(-N)N containing (e.g., hydrazines, hydrazones, or
guanidines, etc.):
This subclass is indented under subclass 564. Subject matter
wherein two nitrogens are singly bonded to each other
(hydrazine or hydrazone grouping) or nitrogens are present
which form the guanidino are present which form the guanidino
grouping (N-C(=N)-N.
Subclass:
566
![[Patents]](../gifs/ps.gif)
Polycarboxylic acid:
This subclass is indented under subclass 864. Subject matter
wherein the active ingredient has at least two C(=O)-O groups
bonded to carbons of the active ingredient.
(1) Note. The O groups can be bonded to the same or
different carbons.
Subclass:
567
![[Patents]](../gifs/ps.gif)
Benzene ring nonionically bonded:
This subclass is indented under subclass 561. Subject matter
wherein the active ingredient contains a benzene ring,
nonionically bonded thereto.
Subclass:
568
![[Patents]](../gifs/ps.gif)
Benzene ring nonionically bonded:
This subclass is indented under subclass 557. Subject matter
wherein the active ingredient contains a benzene ring,
nonionically bonded thereto.
Subclass:
569
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 568. Subject matter
wherein the active ingredient has a fused or bridged ring
system therein which is not ionically bonded.
Subclass:
570
![[Patents]](../gifs/ps.gif)
Carboxy or salt thereof only attached indirectly to the
benzene ring:
This subclass is indented under subclass 568. Subject matter
wherein a carboxyl or salt thereof is attached indirectly to
a benzene ring by nonionic bonding.
(1) Note. If plural benzene rings are present, the carboxyl
or salt thereof must not be directly attached to any of the
benzene rings.
Subclass:
571
![[Patents]](../gifs/ps.gif)
Ether oxygen single bonded to carboxylic acid, percarboxylic
acid or salt thereof through an acyclic carbon or acyclic
carbon chain:
This subclass is indented under subclass 570. Subject mater
wherein the active ingredient contains an ether oxygen single
bonded to a carboxylic or percarboxylic acid group or salt
thereof through an acyclic carbon or acyclic carbon chain,
e.g., contains the group O-C=C-C(O)-OH, etc.
Subclass:
572
![[Patents]](../gifs/ps.gif)
Cyclic carboxylic acid containing three to five carbons or
cyclic percarboxylic acid containing three to five carbons of
salt thereof:
This subclass is indented under subclass 557. Subject mater
wherein the active ingredient contains a nonionically bonded
ring when has exactly 3, 4 or 5 carbon atoms.
Subclass:
573
![[Patents]](../gifs/ps.gif)
Cyclopentyl or cyclopentene (e.g., prostaglandins, etc.):
This subclass is indented under subclass 572. Subject matter
wherein the ring is cyclopentyl or cyclopentene.
(1) Note. This subclass contains certain prostaglandins,
etc.
Subclass:
574
![[Patents]](../gifs/ps.gif)
Polycarboxylic acid or salt thereof:
This subclass is indented under subclass 557. Subject matter
wherein the active ingredient contains at least two C(=O)-O
groups bonded to the same or different carbons.
Subclass:
575
![[Patents]](../gifs/ps.gif)
Hydroxamic acid or salt thereof:
This subclass is indented under subclass 553. Subject matter
wherein the acid is hydroxamic acid on a salt thereof, i.e.,
RC(=O)- NOH, wherein R is hydrogen or an organic radical
bonded to the C=O by a carbon.
Subclass:
576
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 553. Subject matter
wherein the active ingredient contains a benzene ring which
is nonionically bonded.
Subclass:
577
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 576. Subject matter
wherein the active ingredient contains a fused or bridged
ring system which is nonionically bonded.
Subclass:
578
![[Patents]](../gifs/ps.gif)
Acyclic acid or salt thereof:
This subclass is indented under subclass 553. Subject matter
wherein the radical -X-H acid compound is acyclic.
Subclass:
579
![[Patents]](../gifs/ps.gif)
Nitrogen containing other than solely as a nitrogen in an
inorganic ion of an addition salt, a nitro or a nitroso,
DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing nitrogen in a form other
that as nitrogen in an inorganic ion of an addition salt,
nitro or nitroso.
(1) Note. This group of compounds includes for example,
ureas, thioureas, amides, amidines, azines, hydrazones,
carbodimides, oximes, hydroxylamines and amines, inter alia,
as well as their inorganic acid salts.
(2) Note. This subclass is residual for alicyclic amines
not specifically provided for below.
(3) Note. This subclass contains, for example: [figure]
[caption], etc.
(4) Note. If amino nitrogen is present, the compound may
additionally contain nitro, nitroso or nitrogen in an
inorganic ion of an addition salt.
(5) Note. Component parts of an "adduct" will be considered
to be attached to each other ionically, except if it is clear
that the mode of attachment is nonionic.
Subclass:
580
![[Patents]](../gifs/ps.gif)
Thioureas (i.e., N-C(=S)-N:
This subclass is indented under subclass 579. Subject matter
containing the grouping NN.
(1) Note. N=N is not provided for in this subclass; see
appropriate subclass and in particular subclass 631.
Subclass:
581
![[Patents]](../gifs/ps.gif)
Thiocarbazides or thiosemicarbazides (i.e., N-N-C(S=)-N),
containing:
This subclass is indented under subclass 580. Subject matter
containing the thiocarbazide radical, shown in the first
illustration below, or the thiosemicarbazide radical, shown
in the second illustration below. [figure]
Subclass:
582
![[Patents]](../gifs/ps.gif)
Thiocarbazones or thiosemicarbazones (i.e., C=N-N-C(=S)-N)
containing:
This subclass is indented under subclass 581. Subject matter
wherein the compound contains the thiocarbazone radical,
shown in the first illustration, below, or the
thiosemicarbazone radical, shown in the second illustration,
below. [figure]
Subclass:
583
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 582. Subject matter
wherein the compound contains a benzene ring.
Subclass:
584
![[Patents]](../gifs/ps.gif)
C=O, sulfur or cyano attached directly to thiourea nitrogen
by nonionic bonding:
This subclass is indented under subclass 580. Subject matter
wherein a thiourea nitrogen has a carbonyl, sulfur or nitrile
(cyano) group directly attached by nonionic bonding.
Subclass:
585
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 580. Subject matter
wherein the compound contains a benzene ring.
Subclass:
586
![[Patents]](../gifs/ps.gif)
Nitrogen attached indirectly to -C(=S)-group by nonionic
bonding:
This subclass is indented under subclass 585. Subject matter
which contains nitrogen in addition to thiourea nitrogen.
Subclass:
587
![[Patents]](../gifs/ps.gif)
Oxygen containing:
This subclass is indented under subclass 585. Subject matter
which contains oxygen in the compound.
Subclass:
588
![[Patents]](../gifs/ps.gif)
Ureas (i.e., N-C(=O)N:
This subclass is indented under subclass 579. Subject matter
which contains the grouping NN.
(1) Note. This subclass contains, for example, adducts of
urea with inorganic compounds such as hydrogen peroxide or
calcium nitrate.
Subclass:
589
![[Patents]](../gifs/ps.gif)
Nitro or nitroso bonded directly to amino nitrogen (e.g.,
nitramine, nitrosoamine, nitro-urea, etc.):
This subclass is indented under subclass 588. Subject matter
containing a nitro or nitroso group bonded directly to an
amino nitrogen.
Subclass:
590
![[Patents]](../gifs/ps.gif)
Carbazides or semicarbazides (i.e., N-N-C (=O)-N)
containing:
This subclass is indented under subclass 588. Subject matter
containing carbazides or semicarbazides having the grouping
N-N--N-N or N-N--N, respectively.
Subclass:
591
![[Patents]](../gifs/ps.gif)
Biurets (i.e., N-C(=O)-N-C(=O)-N):
This subclass is indented under subclass 588. Subject matter
containing biurets having the grouping NNN.
Subclass:
592
![[Patents]](../gifs/ps.gif)
Sulfur attached directly to urea nitrogen by nonionic
bonding:
This subclass is indented under subclass 588. Subject matter
containing sulfur attached directly to urea nitrogen by
nonionic bonding.
Subclass:
593
![[Patents]](../gifs/ps.gif)
Sulfur is part of a substituent which contains additional
nitrogen:
This subclass is indented under subclass 592. Subject matter
wherein the sulfur is part of a group attached to urea
nitrogen which contains additional nitrogen.
Subclass:
594
![[Patents]](../gifs/ps.gif)
Additional C=O bonded directly to urea nitrogen:
This subclass is indented under subclass 558. Subject matter
wherein a urea nitrogen is directly bonded to a C=O group.
(1) Note. This subclass contains, for example: [figure]
[caption], etc.
Subclass:
595
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 588. Subject matter
containing a benzene ring (i.e., aromatic).
Subclass:
596
![[Patents]](../gifs/ps.gif)
Benzene ring bonded directly to urea nitrogen:
This subclass is indented under subclass 595. Subject matter
wherein a benzene ring is directly bonded to a urea
nitrogen.
Subclass:
597
![[Patents]](../gifs/ps.gif)
Benzene ring is part of a substituent which contains
nitrogen:
This subclass is indented under subclass 596. Subject matter
wherein the benzene ring is part of a substituent which
contains additional nitrogen.
Subclass:
598
![[Patents]](../gifs/ps.gif)
Benzene ring is part of a substituent which contains oxygen:
This subclass is indented under subclass 596. Subject matter
wherein the benzene ring is part of a substituent which
contains oxygen.
Subclass:
599
![[Patents]](../gifs/ps.gif)
Thiocarboxamides (i.e., C(=S)-N):
This subclass is indented under subclass 579. Subject matter
containing thiocarboxamides which have the grouping [figure]
Subclass:
600
![[Patents]](../gifs/ps.gif)
Sulfamides (i.e., N-(O=)S(=O)-N):
This subclass is indented under subclass 579. Subject matter
containing diamides of sulfuric acid (i.e., sulfamides) which
have the grouping [figure]
Subclass:
601
![[Patents]](../gifs/ps.gif)
Sulfonamides (i.e., Q-(O=)S(=O)-N, wherein Q is a substituent
and wherein any substituent attached to nitrogen will be
referred to as E:
This subclass is indented under subclass 579. Subject matter
containing sulfonamides which have the grouping, illustrated
below, wherein Q, E[subscrpt]1[end subscrpt], and
E[subscrpt]2[end subscrpt] are substituents. [figure]
Subclass:
602
![[Patents]](../gifs/ps.gif)
Contains benzene ring:
This subclass is indented under subclass 601. Subject matter
where the sulfonic acid residue is aromatic (i.e., benzene
ring containing).
Subclass:
603
![[Patents]](../gifs/ps.gif)
Nitrogen in Q:
This subclass is indented under subclass 602. Subject matter
wherein the residue of the aromatic sulfonamide contains
nitrogen, e.g., [figure] [caption], etc.
Subclass:
604
![[Patents]](../gifs/ps.gif)
Q is monocyclic:
This subclass is indented under subclass 602. Subject matter
wherein the residue of the aromatic sulfonic acid is
monocyclic, i.e., Q contains only one ring.
Subclass:
605
![[Patents]](../gifs/ps.gif)
Q is acyclic and benzene ring in a substituent E:
This subclass is indented under subclass 601. Subject matter
wherein the sulfonic acid residue contains no ring and the
substituent (E) bonded to the nitrogen portion of the
sulfonamide group contains a benzene ring.
Subclass:
606
![[Patents]](../gifs/ps.gif)
N-S-S containing:
This subclass is indented under subclass 579. Subject matter
which includes thiosulfenamides containing the grouping
N-S-S.
Subclass:
607
![[Patents]](../gifs/ps.gif)
N-S-S containing or contains a nitrogen bonded directly to a
S=O Group (e.g., sulfinamides, etc.):
This subclass is indented under subclass 579. Subject matter
including a compound which contains two amino nitrogen
nonionically bonded directly to the same sulfur or which
contains sulfur doubly bonded to oxygen and directly attached
to an amino nitrogen by nonionic bonding, as for example,
sulfinamides, etc.
Subclass:
608
![[Patents]](../gifs/ps.gif)
Sulfur attached directly to amino nitrogen by nonionic
bonding (e.g., sulfenamides, etc.):
This subclass is indented under subclass 579. Subject matter
containing sulfur bonded directly to an amino nitrogen by
nonionic bonding, as for example sulfenamides.
Subclass:
609
![[Patents]](../gifs/ps.gif)
Cyanamides (i.e., compounds containing cyano bonded directly
to amino nitrogen):
This subclass is indented under subclass 579. Subject matter
containing cyanamides which have a cyano group bonded
directly to an amino nitrogen.
Subclass:
610
![[Patents]](../gifs/ps.gif)
Nitramines (i.e., compounds containing nitro bonded directly
to amino nitrogen):
This subclass is indented under subclass 579. Subject matter
containing nitramines wherein a nitro group is attached
directly to an amino nitrogen.
Subclass:
611
![[Patents]](../gifs/ps.gif)
Nitrosamines (i.e., compounds containing nitroso bonded
directly to amino nitrogen):
This subclass is indented under subclass 579. Subject matter
containing nitrosamines, wherein a nitroso group is attached
directly to an amino nitrogen.
Subclass:
612
![[Patents]](../gifs/ps.gif)
Haloamines (i.e., compounds containing halogen attached
directly to amino nitrogen by nonionic bonding):
This subclass is indented under subclass 579. Subject matter
containing haloamines wherein halogen is attached directly to
an amino nitrogen by nonionic bonding.
Subclass:
613
![[Patents]](../gifs/ps.gif)
Carboxamides (i.e., R-C(=O)-N, wherein r is a radical having
carbon bonded directly to the C(=O)-N or is hydrogen and
wherein any substituent attached to nitrogen will be referred
to as E):
This subclass is indented under subclass 579. Subject matter
including carboxamides which have the grouping RN wherein R
is either a radical having carbon bonded directly to the C=O
or is hydrogen and wherein any substituent attached to
nitrogen will be referred to as E.
Subclass:
614
![[Patents]](../gifs/ps.gif)
N-N containing (e.g., aminimine, hydrazine etc.):
This subclass is indented under subclass 613. Subject matter
which has the N-N grouping, e.g., aminimines, illustrated
below, or another compound with contains the grouping N-N.
[figure] [caption], etc.
Subclass:
615
![[Patents]](../gifs/ps.gif)
R contains benzene ring:
This subclass is indented under subclass 614. Subject matter
wherein the carboxylic acid residue (substituent R) contains
a benzene ring.
Subclass:
616
![[Patents]](../gifs/ps.gif)
Plural carboxamide groups or plural C=O groups bonded
directly to the same nitrogen:
This subclass is indented under subclass 613. Subject matter
containing more than one carboxamide group or containing
plural carbonyls bonded directly to the same nitrogen.
Subclass:
617
![[Patents]](../gifs/ps.gif)
R contains benzene ring:
This subclass is indented under subclass 613. Subject matter
wherein the residue of the carboxylic acid (R) contains a
benzene ring.
Subclass:
618
![[Patents]](../gifs/ps.gif)
Sulfur in R:
This subclass is indented under subclass 613. Subject matter
wherein the residue of the carboxylic acid (R) also contains
sulfur.
Subclass:
619
![[Patents]](../gifs/ps.gif)
Nitrogen in R:
This subclass is indented under subclass 617. Subject matter
wherein the carboxylic acid residue (R) also contains
nitrogen.
Subclass:
620
![[Patents]](../gifs/ps.gif)
The nitrogen in R is an amino nitrogen attached indirectly to
a ring by acyclic bonding:
This subclass is indented under subclass 619. Subject matter
wherein the carboxylic acid residue (R) contains an amine
nitrogen indirectly attached to a ring through a single atom
or through an acyclic chain.
Subclass:
621
![[Patents]](../gifs/ps.gif)
C=O in R:
This subclass is indented under subclass 617. Subject matter
wherein the carboxylic acid residue (R) contains a C=O
group.
Subclass:
622
![[Patents]](../gifs/ps.gif)
C-O group in R:
This subclass is indented under subclass 617. Subject matter
wherein the carboxylic acid residue (R) contains a C-O
group.
Subclass:
623
![[Patents]](../gifs/ps.gif)
Plural alicyclic rings in R:
This subclass is indented under subclass 613. Subject matter
wherein the carboxylic acid residue (R) contains more that
one alicyclic ring.
Subclass:
624
![[Patents]](../gifs/ps.gif)
Three-membered ring in R:
This subclass is indented under subclass 613. Subject matter
wherein the carboxylic acid residue (R) contains a three
membered ring.
Subclass:
625
![[Patents]](../gifs/ps.gif)
R is acyclic:
This subclass is indented under subclass 613. Subject matter
wherein the carboxylic acid residue (R) does not contain a
ring.
Subclass:
626
![[Patents]](../gifs/ps.gif)
Nitrogen in R:
This subclass is indented under subclass 625. Subject matter
wherein the carboxylic acid residue (R) contains nitrogen.
Subclass:
627
![[Patents]](../gifs/ps.gif)
Carbon to carbon unsaturation in R:
This subclass is indented under subclass 625. Subject matter
wherein the carboxylic acid residue (R) contains a double or
triple bond between two carbons.
Subclass:
628
![[Patents]](../gifs/ps.gif)
Halogen bonded directly to carbon in R:
This subclass is indented under subclass 625. Subject matter
wherein the carboxylic acid residue (R) contains halogen
bonded directly to carbon.
Subclass:
629
![[Patents]](../gifs/ps.gif)
R is hydrogen of a lower saturated alkyl of less that seven
carbons:
This subclass is indented under subclass 625. Subject matter
wherein the carboxylic acid residue (R) is from a lower fatty
acid, i.e., a fatty acid of one to seven carbons containing a
C of the carboxy group.
Subclass:
630
![[Patents]](../gifs/ps.gif)
A ring or polycyclo ring system in a substituent E is
attached indirectly to the carboxamide nitrogen or to an
amino nitrogen in substituent E by acyclic nonionic bonding:
This subclass is indented under subclass 629. Subject matter
wherein the amino nitrogen containing residue contains a ring
or a polycyclo ring system which is attached indirectly to
the carboxamide nitrogen or to an additional amino nitrogen
in the amino nitrogen containing residue by acyclic nonionic
bonding.
Subclass:
631
![[Patents]](../gifs/ps.gif)
Amidines (i.e., N=C-N):
This subclass is indented under subclass 579. Subject matter
containing amidines which have the grouping N=C-N.
Subclass:
632
![[Patents]](../gifs/ps.gif)
Amidino hydrazines or hydrazones (i.e., N=C-N-N or N-N=C-N):
This subclass is indented under subclass 631. Subject matter
including a compound which is an amidino hydrazine containing
the grouping N=C-N-N or an amidino hydrazone containing the
grouping O-N=C-N.
Subclass:
633
![[Patents]](../gifs/ps.gif)
Amidoximes (i.e., ON=C-N):
This subclass is indented under subclass 631. Subject matter
which included amidoximes containing the grouping O-N=C-N.
Subclass:
634
![[Patents]](../gifs/ps.gif)
Guanidines (i.e., N=C(-N)-N:
This subclass is indented under subclass 631. Subject matter
which includes guanidines, containing the grouping NN.
Subclass:
635
![[Patents]](../gifs/ps.gif)
Biguanidines (i.e., N=C(-N)-N-(-N)C=N:
This subclass is indented under subclass 634. Subject matter
which includes biguanidines, containing the grouping NNN.
Subclass:
636
![[Patents]](../gifs/ps.gif)
Polyamidines:
This subclass is indented under subclass 631. Subject matter
wherein there is more than one amidine group.
Subclass:
637
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 631. Subject matter
wherein an amidine contains a benzene ring.
Subclass:
638
![[Patents]](../gifs/ps.gif)
Nitrogen double bonded directly to carbon:
This subclass is indented under subclass 579. Subject matter
containing compounds which are characterized by the presence
of the grouping C=N.
Subclass:
639
![[Patents]](../gifs/ps.gif)
Hydrazones (i.e., C=N-N):
This subclass is indented under subclass 638. Subject matter
including the grouping C=N-N.
Subclass:
640
![[Patents]](../gifs/ps.gif)
Oximes (i.e., C=N-O):
This subclass is indented under subclass 638. Subject matter
which includes compounds containing the grouping C=N-O.
Subclass:
641
![[Patents]](../gifs/ps.gif)
Aldimines or ketimines which contain a benzene ring (i.e.,
R-C=N wherein Ri is C or H):
This subclass is indented under subclass 638. Subject matter
which includes aldimines of Ketimines containing a benzene
ring.
(1) Note. This subclass contains compounds having the group
R-C=N wherein the R is either H or a substituent with C
bonded directly to the C of said group.
Subclass:
642
![[Patents]](../gifs/ps.gif)
Quaternary ammonium containing:
This subclass is indented under subclass 579. Subject matter
which contains compounds wherein a pentavalent nitrogen is
bonded by four valences to carbon.
Subclass:
643
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 642. Subject matter
wherein the compound contains a benzene ring.
Subclass:
644
![[Patents]](../gifs/ps.gif)
Amine oxides:
This subclass is indented under subclass 579. Subject matter
which contains compounds characterized by the structure.
Subclass:
645
![[Patents]](../gifs/ps.gif)
Nitroxides, oxyamines or hydroxyamines (i.e., N-O):
This subclass is indented under subclass 579. Subject matter
containing compounds having the grouping N-O.
Subclass:
646
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 579. Subject matter
wherein the compound contains a benzene ring.
Subclass:
647
![[Patents]](../gifs/ps.gif)
Amine nitrogen and a ring bonded directly to the same ring
and any other amino nitrogen in the compound is bonded
directly to one of the rings:
This subclass is indented under subclass 646. Subject matter
wherein a benzene ring is bonded directly to another ring and
at least one amino nitrogen is bonded directly to one of the
rings and any other amino nitrogen in the compound is also
bonded to one of the rings.
(1) Note. This subclass contains compounds having for
example the group: [figure] [caption], etc.
Subclass:
648
![[Patents]](../gifs/ps.gif)
Two aryl rings or aryl ring systems bonded directly to the
same acyclic carbon:
This subclass is indented under subclass 646. Subject matter
wherein two benzene rings or benzene containing polycyclos
are bonded to the same acyclic carbon.
(1) Note. This subclass contains for example the following
group: [figure] [caption], etc.
Subclass:
649
![[Patents]](../gifs/ps.gif)
Amino nitrogen attached to aryl ring or aryl ring system by
an acyclic carbon or acyclic chain:
This subclass is indented under subclass 646. Subject matter
wherein an amino nitrogen is indirectly bonded to an aryl
ring system through a single carbon or through an acyclic
chain.
(1) Note. This subclass includes for example the following
group: [figure] [caption], etc.
Subclass:
650
![[Patents]](../gifs/ps.gif)
The aryl ring system is bonded directly to another ring or
ring system:
This subclass is indented under subclass 649. Subject matter
wherein the aryl ring or ring system is bonded directly to
another ring or ring system.
(1) Note. This subclass contains for example the group:
[figure] [caption], etc.
Subclass:
651
![[Patents]](../gifs/ps.gif)
Ether oxygen is part of the chain:
This subclass is indented under subclass 649. Subject matter
wherein oxygen is a part of the chain.
Subclass:
652
![[Patents]](../gifs/ps.gif)
Alkanol group between the amino nitrogen and an ether oxygen
which is bonded directly to the aryl ring or aryl ring system
(i.e., aryloxy alkanol amines):
This subclass is indented under subclass 651. Subject matter
wherein an alkanol group which is bonded directly to the aryl
ring or aryl ring system.
(1) Note. This subclass includes for example, the group:
[figure] [caption], etc.
SEE OR SEARCH THIS CLASS, SUBCLASS:
651 for a compound containing the group, as shown below:
[figure]
Subclass:
653
![[Patents]](../gifs/ps.gif)
Hydroxy, bonded directly to carbon, attached directly or
indirectly to the acyclic carbon or chain by acyclic nonionic
bonding (e.g., beta hydroxy phenethylamines, etc.):
This subclass is indented under subclass 649. Subject matter
wherein a hydroxy group, which is bonded directly to a
carbon, is attached directly or indirectly to the acyclic
carbon or chain by acyclic nonionic bonding.
Subclass:
654
![[Patents]](../gifs/ps.gif)
The chain consists of two or more carbons which are
unsubstituted or have acyclic hydrocarbyl substituents only:
This subclass is indented under subclass 649. Subject matter
wherein the chain consists of two or more carbons which are
unsubstituted or substituted by acyclic hydrocarbon groups.
Subclass:
655
![[Patents]](../gifs/ps.gif)
The aryl ring or aryl ring system and amino nitrogen are
bonded directly to the same acyclic carbon, which carbon
additionally has only hydrogen or acyclic hydrocarbyl
substituents bonded directly thereto:
This subclass is indented under subclass 649. Subject matter
wherein an aryl ring or ring system and an amino nitrogen are
both directly bonded to the same acyclic carbon which carbon
additionally has only hydrogen or acyclic hydrocarbyl
substituents bonded directly thereto.
Subclass:
656
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 646. Subject matter
which contains a polycyclo ring system.
Subclass:
657
![[Patents]](../gifs/ps.gif)
Bicyclo ring system:
This subclass is indented under subclass 656. Subject matter
wherein the polycyclo ring system is bicyclo.
Subclass:
658
![[Patents]](../gifs/ps.gif)
Two benzene rings bonded directly to the same nitrogen:
This subclass is indented under subclass 646. Subject matter
where two benzene rings are bonded directly to the same
nitrogen.
Subclass:
659
![[Patents]](../gifs/ps.gif)
Alicyclic ring or ring system and amino nitrogen are attached
indirectly by an acyclic carbon or acyclic carbon or acyclic
chain:
This subclass is indented under subclass 579. Subject matter
wherein an amino nitrogen is Indirectly bonded to an
alicyclic ring or ring system through a single acyclic carbon
or through an acyclic chain.
Subclass:
660
![[Patents]](../gifs/ps.gif)
Plural alicyclic rings:
This subclass is indented under subclass 579. Subject matter
wherein there is more than one alicyclic ring.
Subclass:
661
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 660. Subject matter
wherein plural rings are in the form of a polycyclo ring
system.
Subclass:
662
![[Patents]](../gifs/ps.gif)
Tricyclo ring system:
This subclass is indented under subclass 661. Subject matter
wherein the polycyclo ring system contains three rings in the
polycyclo ring system.
Subclass:
663
![[Patents]](../gifs/ps.gif)
Acyclic:
This subclass is indented under subclass 579. Subject matter
wherein the compound contains no ring.
Subclass:
664
![[Patents]](../gifs/ps.gif)
N-N containing (e.g., aminimine, hydrazine, etc.):
This subclass is indented under subclass 663. Subject matter
containing the grouping N-N.
(1) Note. This subclass contains for example the group
[figure] [caption], etc.
Subclass:
665
![[Patents]](../gifs/ps.gif)
Sulfur containing:
This subclass is indented under subclass 663. Subject matter
wherein the compound contains sulfur.
Subclass:
666
![[Patents]](../gifs/ps.gif)
Aldehyde or ketone containing:
This subclass is indented under subclass 663. Subject matter
wherein the compound contains an aldehyde or ketone group.
Subclass:
667
![[Patents]](../gifs/ps.gif)
C-O group containing:
This subclass is indented under subclass 663. Subject matter
which contains a compound with a C-O group.
Subclass:
668
![[Patents]](../gifs/ps.gif)
Polyether:
This subclass is indented under subclass 667. Subject matter
wherein the compound contains more than one C-O-C group.
Subclass:
669
![[Patents]](../gifs/ps.gif)
Polyhydroxy:
This subclass is indented under subclass 667. Subject matter
wherein the compound contains more than one C-OH group.
Subclass:
670
![[Patents]](../gifs/ps.gif)
Monoether:
This subclass is indented under subclass 667. Subject matter
wherein the compound contains only one C-O-C group.
Subclass:
671
![[Patents]](../gifs/ps.gif)
Carbon to carbon unsaturation:
This subclass is indented under subclass 663. Subject matter
wherein the compound contains a double or triple bond between
two carbons.
Subclass:
672
![[Patents]](../gifs/ps.gif)
Halogen bonded directly to carbon:
This subclass is indented under subclass 663. Subject matter
wherein the compound contains a halogen bonded directly to
carbon.
Subclass:
673
![[Patents]](../gifs/ps.gif)
Plural amino nitrogens:
This subclass is indented under subclass 663. Subject matter
wherein the compound contains more than one amino nitrogen.
Subclass:
674
![[Patents]](../gifs/ps.gif)
Three or more amino nitrogens:
This subclass is indented under subclass 673. Subject matter
wherein the compound contains three or more amino nitrogen.
Subclass:
675
![[Patents]](../gifs/ps.gif)
Ketone DOAI:
This subclass is indented under subclass 1. Subject matter
wherein the organic active ingredient is a Ketone.
(1) Note. See section II, Glossary, for the definition of
Ketone.
Subclass:
676
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 675. Subject matter
which contains a nitro or nitroso radical.
Subclass:
677
![[Patents]](../gifs/ps.gif)
Bicyclo ring system having a benzene ring as one of the
cyclos:
This subclass is indented under subclass 676. Subject matter
in which a benzene ring is part of a bicyclo ring system.
Subclass:
678
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 675. Subject matter
which contains a benzene ring.
Subclass:
679
![[Patents]](../gifs/ps.gif)
Plural rings:
This subclass is indented under subclass 678. Subject matter
which contains at least two rings.
Subclass:
680
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 679. Subject matter
which contains a polycyclo ring system.
Subclass:
681
![[Patents]](../gifs/ps.gif)
Bicyclo:
This subclass is indented under subclass 680. Subject matter
wherein the polycyclo ring system is a bicyclo ring system.
Subclass:
682
![[Patents]](../gifs/ps.gif)
Naphthyl ring system:
This subclass is indented under subclass 681. Subject matter
wherein the bicyclo ring system is a naphthyl ring system.
Subclass:
683
![[Patents]](../gifs/ps.gif)
Alicyclic ring:
This subclass is indented under subclass 679. Subject matter
which contains at least one alicyclic ring.
Subclass:
684
![[Patents]](../gifs/ps.gif)
Five-membered alicyclic ring:
This subclass is indented under subclass 683. Subject matter
which contains a five-membered alicyclic ring.
Subclass:
685
![[Patents]](../gifs/ps.gif)
C=O bonded directly to benzene ring:
This subclass is indented under subclass 679. Subject matter
which contains a group directly bonded to a benzene ring.
Subclass:
686
![[Patents]](../gifs/ps.gif)
Two benzene rings bonded directly to the same C=O:
This subclass is indented under subclass 685. Subject matter
wherein two benzene rings are directly bonded to the same
group.
Subclass:
687
![[Patents]](../gifs/ps.gif)
Oxygen single bonded to carbon:
This subclass is indented under subclass 686. Subject matter
which contains C-O group.
Subclass:
688
![[Patents]](../gifs/ps.gif)
C=O bonded directly to benzene ring (e.g., acetophenone,
etc.):
This subclass is indented under subclass 678. Subject matter
wherein is bonded directly to the benzene ring.
Subclass:
689
![[Patents]](../gifs/ps.gif)
Oxygen single bonded to carbon:
This subclass is indented under subclass 688. Subject matter
which contains a C-O- group.
Subclass:
690
![[Patents]](../gifs/ps.gif)
Alicyclic ring containing:
This subclass is indented under subclass 675. Subject matter
which contains an alicyclic ring.
Subclass:
691
![[Patents]](../gifs/ps.gif)
Plural alicyclic ring.
This subclass is indented under subclass 690. Subject matter
which contains more than one alicyclic ring.
Subclass:
692
![[Patents]](../gifs/ps.gif)
Camphor or nuclear substituted derivative thereof:
This subclass is indented under subclass 691. Subject matter
which is camphor, as illustrated below, or a nuclear
substituted derivative thereof. [figure]
Subclass:
693
![[Patents]](../gifs/ps.gif)
Aldehyde DOAI:
This subclass is indented under subclass 1. Subject matter
which includes an aldehyde.
(1) Note. See section II, Glossary, for definition of
aldehyde.
Subclass:
694
![[Patents]](../gifs/ps.gif)
Formaldehyde:
This subclass is indented under subclass 693. Subject matter
containing formaldehyde having the grouping HH.
Subclass:
695
![[Patents]](../gifs/ps.gif)
With polycyclo compound:
This subclass is indented under subclass 694. Subject matter
which also contains a polycyclo compound in admixture
therewith.
Subclass:
696
![[Patents]](../gifs/ps.gif)
With alcohol:
This subclass is indented under subclass 694. Subject matter
which also contains alcohol in admixture therewith.
Subclass:
697
![[Patents]](../gifs/ps.gif)
With nitrogen containing compound:
Subject matter under subject 694 which also contains a
nitrogen containing compound in admixture therewith.
Subclass:
698
![[Patents]](../gifs/ps.gif)
With preservative or stabilizer:
This subclass is indented under subclass 693. Subject matter
which also contains a preserving or stabilizing agent in
admixture therewith.
Subclass:
699
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 693. Subject matter
wherein the compound contains a benzene ring.
Subclass:
700
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 699. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
701
![[Patents]](../gifs/ps.gif)
Acyclic carbon to carbon unsaturation:
This subclass is indented under subclass 699. Subject matter
wherein the compound contains a double or triple bond between
two carbons neither of which is a member of a ring.
Subclass:
702
![[Patents]](../gifs/ps.gif)
Sulfur containing:
This subclass is indented under subclass 693. Subject matter
wherein the compound contains sulfur.
Subclass:
703
![[Patents]](../gifs/ps.gif)
Carbon to carbon unsaturation:
This subclass is indented under subclass 693. Subject matter
wherein the compound contains a double or triple bond between
two carbons.
Subclass:
704
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 693. Subject matter
wherein the compound contains nitrogen.
Subclass:
705
![[Patents]](../gifs/ps.gif)
Plural C=O groups:
This subclass is indented under subclass 693. Subject matter
wherein the compound contains at least two of the following
groups: C=O.
Subclass:
706
![[Patents]](../gifs/ps.gif)
Sulfur, selenium or tellurium compound (e.g., thioalcohols,
mercaptans, etc.) DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing sulfur, selenium or
tellurium.
Subclass:
707
![[Patents]](../gifs/ps.gif)
Persulfide (e.g., R-S-S-R, etc.):
This subclass is indented under subclass 706. Subject matter
in which the sulfur compound is one containing two or more
sulfur atoms joined directly together.
Subclass:
708
![[Patents]](../gifs/ps.gif)
Oxygen bonded directly to sulfur (e.g., sulfoxides, etc.):
This subclass is indented under subclass 706. Subject matter
wherein the compound contains oxygen directly bonded to
sulfur.
(1) Note. This subclass includes sulfoxides (S=O) for
example.
Subclass:
709
![[Patents]](../gifs/ps.gif)
Plural oxygens bonded directly to the same sulfur (e.g.,
sulfones, etc.):
This subclass is indented under subclass 708. Subject matter
wherein at least two oxygens are directly bonded to the same
sulfur atom.
(1) Note. This subclass includes sulfones (O=S=O) for
example.
Subclass:
710
![[Patents]](../gifs/ps.gif)
Acyclic carbon to carbon unsaturation:
This subclass is indented under subclass 709. Subject matter
wherein the compound contains a double or triple bond between
two carbons neither of which is a member of a ring.
Subclass:
711
![[Patents]](../gifs/ps.gif)
Acyclic:
This subclass is indented under subclass 708. Subject matter
wherein the compound does not contain a ring.
Subclass:
712
![[Patents]](../gifs/ps.gif)
Thioether:
This subclass is indented under subclass 706. Subject matter
in which the compound has the R-S-R structure wherein the R's
are diverse or identical organic radicals.
Subclass:
713
![[Patents]](../gifs/ps.gif)
Acyclic carbon to carbon unsaturation:
This subclass is indented under subclass 712. Subject matter
wherein the compound contains a double or triple bond between
two carbons neither of which is a member of a ring.
Subclass:
714
![[Patents]](../gifs/ps.gif)
Peroxide DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing an O-O group.
Subclass:
715
![[Patents]](../gifs/ps.gif)
Ether DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing an oxygen atom which is
bonded to carbons of two discrete organic radicals and has
the grouping R-O-R wherein the R's are diverse or identical
organic radicals.
Subclass:
716
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 715. Subject matter
wherein the compound contains nitrogen.
Subclass:
717
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 715. Subject matter
wherein the compound contains a benzene ring.
Subclass:
718
![[Patents]](../gifs/ps.gif)
Plural oxygens:
This subclass is indented under subclass 717. Subject matter
wherein the compound contains at least two oxygen atoms.
Subclass:
719
![[Patents]](../gifs/ps.gif)
Alicyclic ring:
This subclass is indented under subclass 718. Subject matter
wherein the compound contains an alicyclic ring.
Subclass:
720
![[Patents]](../gifs/ps.gif)
Acyclic carbon to carbon unsaturation:
This subclass is indented under subclass 718. Subject matter
wherein the compound contains a double or triple bond between
two carbons neither of which is a member of a ring.
Subclass:
721
![[Patents]](../gifs/ps.gif)
Plural benzene rings:
This subclass is indented under subclass 718. Subject matter
wherein the compound contains two or more benzene rings.
Subclass:
722
![[Patents]](../gifs/ps.gif)
Acyclic:
This subclass is indented under subclass 715. Subject matter
wherein the compound does not contain a ring.
Subclass:
723
![[Patents]](../gifs/ps.gif)
Plural oxygens:
This subclass is indented under subclass 722. Subject matter
wherein the compound contains at least two oxygen atoms.
Subclass:
724
![[Patents]](../gifs/ps.gif)
C-O group (e.g., alcohol, alcoholate, etc.) DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing a C-O- group.
Subclass:
725
![[Patents]](../gifs/ps.gif)
Vitamin a compound or derivative:
This subclass is indented under subclass 724. Subject matter
wherein the compound is vitamin A or the alcoholates thereof.
See illustration below. [figure]
Subclass:
726
![[Patents]](../gifs/ps.gif)
Diphenyl-substituted acyclic alcohol or alcoholate:
This subclass is indented under subclass 724. Subject matter
in which a hydroxyl group is attached to a single carbon
atom, or to a chain of two or more carbon atoms, which link
two phenyl groups.
(1) Note. This subclass contains, for example: [figure]
[caption]and [figure]
Subclass:
727
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 724. Subject matter
wherein the compound contains nitrogen.
Subclass:
728
![[Patents]](../gifs/ps.gif)
C of C-O- group is nuclear C of a benzene ring (e.g., phenol,
phenolate, etc.):
This subclass is indented under subclass 727. Subject matter
wherein the C-O- group of the compound is a group, i.e., the
carbon of the C-O group is a nuclear carbon of a benzene
ring. See illustration below. [figure]
Subclass:
729
![[Patents]](../gifs/ps.gif)
Alicyclic ring containing:
This subclass is indented under subclass 724. Subject matter
wherein the compound contains an alicyclic ring.
Subclass:
730
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 724. Subject matter
wherein the compound contains a benzene ring.
Subclass:
731
![[Patents]](../gifs/ps.gif)
C of C-O- group is nuclear C of a benzene ring (e.g., phenol,
phenolate, etc.):
This subclass is indented under subclass 730. Subject matter
wherein the C-O- group of the compound is a group, i.e., the
carbon of the C-O- group is a nuclear carbon of a benzene
ring. See illustration below. [figure]
Subclass:
732
![[Patents]](../gifs/ps.gif)
Polycyclo ring system (e.g., naphthols, etc.):
This subclass is indented under subclass 731. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
733
![[Patents]](../gifs/ps.gif)
Acyclic carbon to carbon unsaturation:
This subclass is indented under subclass 731. Subject matter
wherein the compound contains a double or triple bond between
two carbons neither of which is a member of a ring.
Subclass:
734
![[Patents]](../gifs/ps.gif)
Two or more separate aryl-O- groups:
This subclass is indented under subclass 731. Subject matter
wherein the compound contains at least two groups as
illustrated below. [figure]
(1) Note. This subclass is not satisfied by the group,
illustrated below, alone. [figure]
Subclass:
735
![[Patents]](../gifs/ps.gif)
Nuclear halogenated:
This subclass is indented under subclass 734. Subject matter
wherein the compound contains a halogen bonded directly to a
nuclear carbon of a benzene ring.
Subclass:
736
![[Patents]](../gifs/ps.gif)
Additional benzene ring containing:
This subclass is indented under subclass 731. Subject matter
wherein the compound contains at least one benzene ring in
addition to the group, as illustrated below. [figure]
Subclass:
737
![[Patents]](../gifs/ps.gif)
Nuclear halogenated:
This subclass is indented under subclass 731. Subject matter
wherein the compound contains a halogen bonded directly to a
nuclear carbon of a benzene ring.
Subclass:
738
![[Patents]](../gifs/ps.gif)
Polyhydroxy:
This subclass is indented under subclass 724. Subject matter
wherein the compound contains at least two -OH groups.
Subclass:
739
![[Patents]](../gifs/ps.gif)
Carbon to carbon unsaturation:
This subclass is indented under subclass 724. Subject matter
wherein the compound contains a double or triple bond between
two carbon atoms.
Subclass:
740
![[Patents]](../gifs/ps.gif)
Nitrogen containing compound DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound containing a nitrogen atom.
Subclass:
741
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 740. Subject matter
wherein the compound contains a benzene ring.
Subclass:
742
![[Patents]](../gifs/ps.gif)
Polynitro:
This subclass is indented under subclass 740. Subject matter
wherein the compound contains at least two -NO[subscrpt]2[end
subscrpt] groups.
Subclass:
743
![[Patents]](../gifs/ps.gif)
Halogenated hydrocarbon DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound consisting of carbon, hydrogen and
halogen atoms or only of carbon and halogen atoms.
Subclass:
744
![[Patents]](../gifs/ps.gif)
Unsaturated aliphatic compound:
This subclass is indented under subclass 743. Subject matter
wherein the compound contains no rings and contains a double
or triple bond between two carbon atoms.
Subclass:
745
![[Patents]](../gifs/ps.gif)
Alkyne:
This subclass is indented under subclass 744. Subject matter
wherein the compound contains a triple bond between two
carbon atoms.
Subclass:
746
![[Patents]](../gifs/ps.gif)
Plural halogenated hydrocarbon compounds:
This subclass is indented under subclass 744. Subject matter
wherein there is more than one halogenated hydrocarbon
compound.
Subclass:
747
![[Patents]](../gifs/ps.gif)
Carbocyclic:
This subclass is indented under subclass 743. Subject matter
wherein the halogenated hydrocarbon contains a ring in which
all ring members are carbons.
Subclass:
748
![[Patents]](../gifs/ps.gif)
Two benzene rings directly attached to an acyclic hydrocarbon
or acyclic halogenated hydrocarbon (e.g., D.D.T., etc.):
This subclass is indented under subclass 747. Subject matter
wherein the compound contains two phenyl substituents on an
acyclic hydrocarbon or acyclic halogenated hydrocarbon and
the phenyl groups are connected only through a carbon chain
of the acyclic group.
Subclass:
749
![[Patents]](../gifs/ps.gif)
Fluorine containing:
This subclass is indented under subclass 748. Subject matter
wherein the compound contains fluorine.
Subclass:
750
![[Patents]](../gifs/ps.gif)
With organic ether or -OH containing compound, non-DOAI:
This subclass is indented under subclass 748. Subject matter
wherein there is an organic ether or -OH containing non-DOAI
compound in addition to the halogenated hydrocarbon
compound.
Subclass:
751
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 747. Subject matter
wherein the compound contains a benzene ring.
Subclass:
752
![[Patents]](../gifs/ps.gif)
Alkyne:
This subclass is indented under subclass 751. Subject matter
wherein the compound contains a triple bond between two
carbon atoms.
Subclass:
753
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 751. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
754
![[Patents]](../gifs/ps.gif)
Plural benzene rings:
This subclass is indented under subclass 751. Subject matter
wherein the compound contains at least two benzene rings.
Subclass:
755
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 747. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
756
![[Patents]](../gifs/ps.gif)
Bicyclo:
This subclass is indented under subclass 755. Subject matter
wherein the polycyclo ring system consists of exactly two
rings.
Subclass:
757
![[Patents]](../gifs/ps.gif)
Two or more halogenated hydrocarbons:
This subclass is indented under subclass 743. Subject matter
which includes at least two halogenated hydrocarbon
compounds.
Subclass:
758
![[Patents]](../gifs/ps.gif)
Chlorine as only halogen:
This subclass is indented under subclass 743. Subject matter
wherein the halogenated hydrocarbon compound contains
chlorine and no other halogen atoms.
Subclass:
759
![[Patents]](../gifs/ps.gif)
Fluorine as only halogen:
This subclass is indented under subclass 743. Subject matter
wherein the halogenated hydrocarbon contains only fluorine
halogen atoms.
Subclass:
760
![[Patents]](../gifs/ps.gif)
Bromine and chlorine as only halogens:
This subclass is indented under subclass 743. Subject mater
wherein the halogenated hydrocarbon contains bromine and
chlorine atoms and no other halogen atoms.
Subclass:
761
![[Patents]](../gifs/ps.gif)
Bromine and fluorine as only halogens:
This subclass is indented under subclass 743. Subject matter
wherein the halogenated hydrocarbon contains bromine and
fluorine atoms and no other halogen atoms.
Subclass:
762
![[Patents]](../gifs/ps.gif)
Hydrocarbon DOAI:
This subclass is indented under subclass 1. Subject matter
which includes a compound consisting of carbon and hydrogen
atoms only.
Subclass:
763
![[Patents]](../gifs/ps.gif)
Carbocyclic:
This subclass is indented under subclass 762. Subject matter
wherein the compound contains at least one ring in which all
of the members are carbon.
Subclass:
764
![[Patents]](../gifs/ps.gif)
Benzene ring containing:
This subclass is indented under subclass 763. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
765
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 764. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
766
![[Patents]](../gifs/ps.gif)
Polycyclo ring system:
This subclass is indented under subclass 763. Subject matter
wherein the compound contains a polycyclo ring system.
Subclass:
767
![[Patents]](../gifs/ps.gif)
With phosphorus containing non-DOAI:
This subclass is indented under subclass 762. Subject matter
which also contains a non-DOAI phosphorus atom or compound in
admixture therewith.
Subclass:
768
![[Patents]](../gifs/ps.gif)
With sulfur containing non-DOAI:
This subclass is indented under subclass 762. Subject matter
which also contains a non-DOAI sulfur atom of compound in
admixture therewith.
Subclass:
769
![[Patents]](../gifs/ps.gif)
DESIGNATED INORGANIC NONACTIVE INGREDIENT OR ELEMENTAL
MATERIAL OTHER THAT WATER:
This subclass is indented under the class definition.
Subject matter wherein the composition contains an organic
nonactive ingredient or elemental material other than water.
(1) Note. This and indented subclasses provide for
compositions which (a) do not contain a designated
pharmacologically or biologically active ingredient or which
(b) are solely disclosed or claimed as useful as inert
additives or carriers for an active ingredient of this class,
e.g., diluent or carrier.
(2) Note. Within this subclass are compositions which may
contain an organic active ingredient which does not meet the
definition of the designated organic active ingredient
(DOAI).
(3) Note. See section II, Glossary, for the definition
"DOAI".
(4) Note. A Claim of the type: "A pharmaceutical
composition containing a medicament or drug and l-20 percent
by weight of aluminum oxide and 5-20 percent by weight of
sodium bicarbonate" is properly classified under the
subclass.
Subclass:
770
![[Patents]](../gifs/ps.gif)
Siliceous or calcareous material (e.g., cloy, earth, etc.):
This subclass is indented under subclass 769. Subject matter
wherein the nonbioactive inorganic compound contains silicon
or calcium, e.g., clays, etc.
Subclass:
771
![[Patents]](../gifs/ps.gif)
Oxygen gas containing:
This subclass is indented under subclass 769. Subject matter
which contains oxygen gas.
Subclass:
772
![[Patents]](../gifs/ps.gif)
DESIGNATED ORGANIC NONACTIVE INGREDIENT CONTAINING OTHER THAN
HYDROCARBON:
This subclass is indented under the class definition.
Subject matter wherein the composition contains a
nonbioactive organic compound.
(1) Note. This and indented subclasses provide for
compositions which (a) do not contain a pharmacologically or
biologically active ingredient or which (b) are solely
disclosed or claimed as useful as inert additives or carriers
for an active ingredient of this class. For example:
topical preparations, e.g., face cream, etc., which are not
specifically provided for as special subclasses and which do
not contain a designated active ingredient are classified in
this and indented subclasses.
(2) Note. Within this subclass are compositions which may
contain an organic active ingredient which does not meet the
definition of the designated organic active ingredient
(DOAI).
(3) Note. See section II, Glossary, for the definition of
"DOAI".
(4) Note. A claim of the type: "A pharmaceutical
composition containing a medicament or drug and 1-20 percent
by weight glycerin, 1-10 percent by weight ethyl alcohol and
5-10 percent by weight of an cationic surfactant" is properly
classified under this subclass.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, appropriate subclasses for subject matter
relating to: colloid systems (such as sols*, emulsions,
dispersions, foams, aerosols, smokes, gels, or pastes) or
wetting agents (such as leveling, penetrating, or spreading);
subcombination compositions of colloid systems containing at
least an agent specialized and designed for or peculiar to
use in making or stabilizing colloid systems; compositions
and subcombination compositions specialized and designed for
or peculiar to use in breaking (resolving) or inhibiting
colloid systems; processes of making the compositions or
systems of the class; processes of breaking (resolving) or
inhibiting colloid systems; in each instance, when
generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
772.1
![[Patents]](../gifs/ps.gif)
Aftertreated solid synthetic organic polymer (e.g., grafting,
blocking, etc.):
This subclass is indented under subclass 772. Subject matter
wherein the designated organic nonactive ingredient is a
solid synthetic organic polymer which has been aftertreated,
e.g., a saponified starch acrylonitrile graft copolymer,
polyacrylic acid neutralized with sodium hydroxide, etc.
(1) Note. The chemical after treatment of a solid synthetic
organic polymer may be to remove or add a group or element or
a combination of both procedures.
SEE OR SEARCH CLASS:
522, Synthetic Resins or Natural Rubbers, for the process of
treating a solid polymer utilizing wave energy.
525, Synthetic Resins or Natural Rubbers, appropriate
subclasses for the aftertreatment of solid synthetic organic
polymers.
Subclass:
772.2
![[Patents]](../gifs/ps.gif)
Polyvinyl alcohol:
This subclass is indented under subclass 772.1. Subject
matter wherein the solid polymer is polyvinyl alcohol, e.g.,
obtained from the hydrolysis of polyvinyl acetate or
copolymers thereof, etc.
Subclass:
772.3
![[Patents]](../gifs/ps.gif)
Solid synthetic organic polymer:
This subclass is indented under subclass 772. Subject matter
wherein the designated organic nonactive ingredient is a
solid synthetic polymer, e.g., a pharmaceutical preparation
containing a bio-degradable polymer derived from a monomer
mixture comprising 2, 2-bis (epsilon-caprolactone-4-yl)
propane, gamma-valerolactone and epsilon-caprolactone, etc.
SEE OR SEARCH THIS CLASS, SUBCLASS:
78.01 for a pharmaceutical composition which contains a
solid synthetic organic polymer which functions as a
designated organic active ingredient.
78.08 for a more thorough discussion on polymers which are
proper for Classes 424, 514, and Class 520 Series.
SEE OR SEARCH CLASS:
522, Synthetic Resins or Natural Rubbers, for the process of
preparing a solid polymer utilizing wave energy.
526, Synthetic Resins or Natural Rubbers, for the perparation
of solid synthetic polymers derived from ethylenic monomers
only, e.g., acrylic acid, etc.
527, Synthetic Resins or Natural Rubbers, for the preparation
of solid synthetic polymers derived from the reaction between
a natural product and other chemical intermediates, e.g., a
carbohydrate and polyisocyanate, a protein and an ethylenic
reactant, etc.
528, Synthetic Resins or Natural Rubbers, 1 for the
preparation of a solid synthetic polymer derived from at
least one saturated reactant, e.g., toluene diisocyanate and
polyethylene glycol, etc.; subclasses 480+ treating a solid
polymer merely with heat.
Subclass:
772.4
![[Patents]](../gifs/ps.gif)
Polymer from ethylenic monomers only:
This subclass is indented under subclass 772.3. Subject
matter wherein the polymer is derived from ethylenic monomers
only, e.g., a self-microencapsulating pesticidal composition
contains polymethyl methacrylate, a cosmetic moisturizing
composition contains a copolymer from acrolein and sodium
acrylate, etc.
(1) Note. See Class 424, subclass 78.17 for the definition
of an ethylenic monomer.
Subclass:
772.5
![[Patents]](../gifs/ps.gif)
Heterocyclic monomer:
This subclass is indented under subclass 772.4. Subject
matter wherein the solid polymer is derived from a
heterocyclic monomer, e.g., a cosmetic composition containing
a copolymer derived from vinyl ether and maleic anhydride, a
cosmetic emulsion containing a copolymer derived from
vinylpyrrolidone, vinyl acetate, and vinyl myristate, etc.
Subclass:
772.6
![[Patents]](../gifs/ps.gif)
Carboxylic acid containing monomer:
This subclass is indented under subclass 772.4. Subject
matter wherein the solid polymer is derived from an
ethylenically unsaturated monomer containing a carboxylic
acid group, e.g., acrylic acid, maleic acid, fumaric acid,
etc.
Subclass:
772.7
![[Patents]](../gifs/ps.gif)
Heterocyclic monomer:
This subclass is indented under subclass 772.3. Subject
matter wherein the solid polymer is derived from a
heterocyclic monomer, e.g., ethylene oxide, etc.
Subclass:
773
![[Patents]](../gifs/ps.gif)
Peptide containing:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound is a peptide which
is not degraded to the constituent amino acids, e.g.,
collagen, etc.
Subclass:
774
![[Patents]](../gifs/ps.gif)
Gelatin or derivative:
This subclass is indented under subclass 773. Subjects
matter wherein the peptide is gelatin or a derivative
thereof.
Subclass:
775
![[Patents]](../gifs/ps.gif)
Casein (milk protein) or derivative:
This subclass is indented under subclass 773. Subject matter
wherein the peptide is casein (milk protein) or a derivative
thereof.
Subclass:
776
![[Patents]](../gifs/ps.gif)
Albumin or derivative:
This subclass is indented under subclass 773. Subject matter
wherein the peptide is albumin or a derivative thereof.
Subclass:
777
![[Patents]](../gifs/ps.gif)
Carbohydrate or lignin, or derivative:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound is a carbohydrate
or lignin or derivative thereof wherein the carbon skeleton
of the carbohydrate is not destroyed except as noted below.
(1) Note. Alcohols and acids corresponding to carbohydrates
are excluded from this subclass and compositions containing
such compounds are in appropriate subclasses below.
(2) Note. Lignin is a noncarbohydrate, polymeric substance
found in wood. It is isolated directly from wood or wood
products or from the compositions derived from the treatment
of wood, e.g., waste sulfite liquor or black liquor. The
structure of the lignin monomer is not completely know.
Subclass:
778
![[Patents]](../gifs/ps.gif)
Starch or derivative:
This subclass is indented under subclass 777. Subject matter
wherein the carbohydrate is a starch or derivative thereof.
Subclass:
779
![[Patents]](../gifs/ps.gif)
Algin or derivative:
This subclass is indented under subclass 777. Subject matter
wherein the carbohydrate is algin or a derivative thereof.
Subclass:
780
![[Patents]](../gifs/ps.gif)
Locust bean gum:
This subclass is indented under subclass 777. Subject matter
wherein the carbohydrate is locust bean gum.
Subclass:
781
![[Patents]](../gifs/ps.gif)
Cellulose of derivative:
This subclass is indented under subclass 777. Subject matter
wherein the carbohydrate is cellulose or a derivative
thereof.
Subclass:
782
![[Patents]](../gifs/ps.gif)
Natural gum or resin:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound is a natural gum or
resin, e.g., natural rubber, latex, rosin, etc.
Subclass:
783
![[Patents]](../gifs/ps.gif)
Plant extract or plant material of undetermined
constitution:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound is a plant extract
of plant product of undetermined chemical constitution
including essential oils.
(1) Note. An extract is considered to be of determined
constitution when sufficient information as to its chemical
structure is available to permit classification based upon
its chemical structure.
Subclass:
784
![[Patents]](../gifs/ps.gif)
Carboxylic acid or salt thereof:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound is a carboxylic
acid or salt thereof.
Subclass:
785
![[Patents]](../gifs/ps.gif)
Carboxylic acid ester:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound is an ester of a
carboxylic acid.
Subclass:
786
![[Patents]](../gifs/ps.gif)
Glyceride:
This subclass is indented under subclass 785. Subject matter
wherein the ester is derived from glycerol.
(1) Note. The fats and oils and mainly triglycerides of
fatty acids, e.g., tripalmitin.
Subclass:
787
![[Patents]](../gifs/ps.gif)
Beeswax:
This subclass is indented under subclass 785. Subject matter
wherein the ester is beeswax.
Subclass:
788
![[Patents]](../gifs/ps.gif)
Nitrogen containing:
This subclass is indented under subclass 772. Subject matter
wherein the nonbioactive organic compound contains nitrogen,
e.g., amines or amides.
Subclass:
788.1
![[Patents]](../gifs/ps.gif)
SOLID SYNTHETIC ORGANIC POLYMER DERIVED SOLELY FROM
HYDROCARBON REACTANTS AS DESIGNATED ORGANIC NONACTIVE
INGREDIENT CONTAINING:
This subclass is indented under the class definition.
Subject matter wherein the composition contains a solid
synthetic organic polymer derived solely from hydrocarbon
reactants, e.g., polystyrene, etc.
SEE OR SEARCH CLASS:
424, Drug, Bio-Affecting and Body Treating Compositions,
78.01 for a pharmaceutical composition which contains a
solid synthetic organic polymer which functions as a
designated organic active ingredient; subclass 78.08 for a
more thorough discussion on polymers which are proper for
Classes 424, 514 and 520 Series.
Subclass:
789
![[Patents]](../gifs/ps.gif)
MISCELLANEOUS (E.G., HYDROCARBONS, ETC.):
This subclass is indented under the class definition.
Subject matter not otherwise provided for, e.g.,
hydrocarbons, etc.
CROSS-REFERENCE ART COLLECTIONS
(1) Note. The following subclasses are collections of
published disclosures pertaining to various specified aspects
relating to drug, bioaffecting and body treating compositions
and which aspects do not form appropriate bases for
subclasses in the foregoing classification (i.e., subclasses
superior hetero in the schedule). These disclosures relate
to Class 514 subject matter only.
(2) Note. The general outline of the developed
cross-reference art collections is as follows:
(A) Subclasses 800-809 provide for disclosures relating to
PEPTIDE AND PROTEIN.
(B) Subclasses 810-935 provide for disclosures drawn to
SPECIFICALLY DISCLOSES DISEASE CONDITION AND PHARMACEUTICAL
EFFECT.
(1) This are collection will take patents dating from
January, 1965 to date, e.g., Classes 71, 424, 514, 260, and
the 530-570 series, etc.
(2) References crossed into this are collection should have
specific, disclosed compositions or examples of use. A mere
statement or mention of a utility or composition, unless
actually claimed, is generally insufficient.
(C) Subclasses 936-975 are drawn to a number of various art
concepts.
(1) Subclasses 936-947 drawn to LIQUID CARRIER, DILUENT OR
SOLVENT, subclasses 948-956 drawn to SOLID CARRIER OR SOLID
DILUENT, subclasses 957-959 drawn to GASEOUS OR GAS EMITTING
CARRIER OR PROPELLANT, subclasses 960-965 drawn to PILL,
LOZENGE, TABLET OR CAPSULE, subclasses 966-969 drawn to
SUPPOSITORY BOUGIE OR BASE, subclasses 970-975 drawn to
SPECIAL DESIGNATED INGREDIENT.
(2) These art collections provide (a) data from Class 260
(Compounds) and Classes 530-570 series and Class 585 dating
from January 1, 1965, (b) and data from all other classes
regardless of date.
(3) References crosses into these art collections should
have specific, disclosed compositions or methods where the
inventive concept or point of novelty resides in the carrier
system, the form of the composition or have designated
ingredients, e.g., stabilizers, etc.
Subclass:
800
![[Patents]](../gifs/ps.gif)
LHRH LIKE:
Subject matter involving a compositions containing peptides
that influence the release of lutenizing hormone.
Subclass:
801
![[Patents]](../gifs/ps.gif)
COLLAGEN, GELATIN OR DERIVATIVE THEREOF:
Subject matter wherein the peptide composition contain
collagen, gelatin of derivative.
Subclass:
802
![[Patents]](../gifs/ps.gif)
FIBRINOPEPTIDES, BLOOD-COAGULATION FACTORS OR DERIVATIVE:
Subject matter wherein the peptide composition is related to
fibrinopeptides, blood-coagulation factors or derivative.
Subclass:
803
![[Patents]](../gifs/ps.gif)
KININ OR DERIVATIVE:
Subject matter wherein the peptide composition has Kinin-like
activities.
Subclass:
804
![[Patents]](../gifs/ps.gif)
PHLEOMYCIN SERIES OR DERIVATIVE:
Subject matter containing a phleomycin peptide or
derivative.
Subclass:
805
![[Patents]](../gifs/ps.gif)
ADRENOCORTICOTROPIC HORMONE OR DERIVATIVE:
Subject matter involving peptide composition having
adrenocorticotropic activity.
Subclass:
806
![[Patents]](../gifs/ps.gif)
SOMATOSTATIN OR DERIVATIVE:
Subject matter involving peptide compositions having
somatostatin-like activity.
Subclass:
807
![[Patents]](../gifs/ps.gif)
OXYTOXIN, VASOPRESSIN OR DERIVATIVE:
Subject matter involving peptide composition related to
oxytoxin, vasopressin or a derivative thereof.
Subclass:
808
![[Patents]](../gifs/ps.gif)
CALCITONIN OR DERIVATIVES:
Subject matter involving peptide composition related to
calcitonin or a derivative thereof.
Subclass:
809
![[Patents]](../gifs/ps.gif)
ENKEPHALIN, ENDORPHIN OR DERIVATIVES:
Subject matter involving neurological peptides related to
enkephalin or endorphin.
Subclass:
810
![[Patents]](../gifs/ps.gif)
ADDICTION:
Subject matter involving the treatment of the state of being
devoted or given up to a practice or habit or to something
habit forming to the extent that cessation causes severe
trauma.
Subclass:
811
![[Patents]](../gifs/ps.gif)
Alcohol:
This subclass is indented under subclass 810. Subject matter
wherein the addictive substance is alcohol.
Subclass:
812
![[Patents]](../gifs/ps.gif)
Narcotic:
This subclass is indented under subclass 810. Subject matter
wherein the addictive substance is a narcotic.
Subclass:
813
![[Patents]](../gifs/ps.gif)
Tobacco:
This subclass is indented under subclass 810. Subject matter
wherein the addictive substance is tobacco.
Subclass:
814
![[Patents]](../gifs/ps.gif)
ANEMIA:
Subject matter involving the treatment of anemia.
Subclass:
815
![[Patents]](../gifs/ps.gif)
Sickle cell:
This subclass is indented under subclass 814. Subject matter
wherein the anemic condition is sickle cell anemia.
Subclass:
816
![[Patents]](../gifs/ps.gif)
ANESTHETIC, GENERAL:
Subject matter involving a general anesthetic effect.
Subclass:
817
![[Patents]](../gifs/ps.gif)
ANESTHETIC, TOPICAL:
Subject matter involving a topical anesthetic effect.
Subclass:
818
![[Patents]](../gifs/ps.gif)
ANESTHETIC, LOCAL:
Subject matter involving a local anesthetic effect.
Subclass:
819
![[Patents]](../gifs/ps.gif)
ANTACID, ORAL:
Subject matter involving an antacid effect when administered
orally.
Subclass:
820
![[Patents]](../gifs/ps.gif)
With antiflatulent:
This subclass is indented under subclass 819. Subject matter
wherein an ingredient to yield an antiflatulent effect is
also present.
Subclass:
821
![[Patents]](../gifs/ps.gif)
ANTIARRHYTHMIC:
Subject matter involving the treatment or prevention of
arrhythmia in a patient in need thereof.
Subclass:
822
![[Patents]](../gifs/ps.gif)
ANTICOAGULATION:
Subject matter involving an anticoagulation effect.
Subclass:
823
![[Patents]](../gifs/ps.gif)
ANTIDOTE:
Subject matter involving an antidote (prevents or
counteracts) for a poison or other noxious substance.
Subclass:
824
![[Patents]](../gifs/ps.gif)
ARTERIOSCLEROSIS:
Subject matter involving treatment of arteriosclerosis.
Subclass:
825
![[Patents]](../gifs/ps.gif)
ARTHRITIS:
Subject matter involving treatment of arthritis.
Subclass:
826
![[Patents]](../gifs/ps.gif)
ASTHMA:
Subject matter involving treatment or alleviation of the
symptoms of asthma.
Subclass:
827
![[Patents]](../gifs/ps.gif)
ASTRINGENT, NONFACIAL:
Subject matter involving an astringent effect.
Subclass:
828
![[Patents]](../gifs/ps.gif)
Topical for the skin:
This subclass is indented under subclass 827. Subject matter
wherein the astringent is applied topically to the skin.
Subclass:
829
![[Patents]](../gifs/ps.gif)
BITE OR STING:
Subject matter involving the treatment or alleviation of
discomfort or other symptoms caused by a bite or sting.
Subclass:
830
![[Patents]](../gifs/ps.gif)
Insect:
This subclass is indented under subclass 829. Subject matter
wherein the bite or sting is from an insect.
Subclass:
831
![[Patents]](../gifs/ps.gif)
Animal (nonpoisonous):
This subclass is indented under subclass 829. Subject matter
wherein the bite or sting is from a nonpoisonous animal.
Subclass:
832
![[Patents]](../gifs/ps.gif)
BLOOD SUBSTITUTE:
Subject matter involving a substance which is a substitute
for blood or blood component.
Subclass:
833
![[Patents]](../gifs/ps.gif)
BLOOD PLASMA EXTENDER:
Subject matter involving extending or increasing the amount
of blood plasma in a patient in need thereof.
Subclass:
834
![[Patents]](../gifs/ps.gif)
COAGULANT:
Subject matter involving the enhancing of coagulation.
Subclass:
835
![[Patents]](../gifs/ps.gif)
CARIES:
Subject matter involving treatment or prevention of caries.
Subclass:
836
![[Patents]](../gifs/ps.gif)
CHELATE:
Subject matter involving a material which acts as a chelating
agent.
Subclass:
837
![[Patents]](../gifs/ps.gif)
CHOLERA:
Subject matter involving the treatment or prevention of
cholera.
Subclass:
838
![[Patents]](../gifs/ps.gif)
CIRRHOSIS:
Subject matter involving the treatment or alleviation of the
symptoms of cirrhosis of the liver.
Subclass:
839
![[Patents]](../gifs/ps.gif)
CONTACT LENS TREATMENT:
Subject matter involving treatment of contact lens such as
sterilization or cleaning.
Subclass:
840
![[Patents]](../gifs/ps.gif)
CHEMICAL STERILIZING:
This subclass is indented under subclass 839. Subject matter
wherein a chemical agent is used for sterilizing the contact
lens.
Subclass:
841
![[Patents]](../gifs/ps.gif)
CONTRACEPTIVE:
Subject matter involving prevention of conception.
Subclass:
842
![[Patents]](../gifs/ps.gif)
Nonmammal:
This subclass is indented under subclass 841. Subject matter
wherein conception is prevented in nonmammals, e.g., insects,
etc.
Subclass:
843
![[Patents]](../gifs/ps.gif)
Female (mammal):
This subclass is indented under subclass 841. Subject matter
wherein conception is prevented in a female mammal.
Subclass:
844
![[Patents]](../gifs/ps.gif)
COSMETIC, FACIAL:
Subject matter involving facial cosmetics.
Subclass:
845
![[Patents]](../gifs/ps.gif)
Liquid make-up:
This subclass is indented under subclass 844. Subject matter
wherein the cosmetic is a liquid make-up.
Subclass:
846
![[Patents]](../gifs/ps.gif)
Cleansing cream or lotion:
This subclass is indented under subclass 844. Subject matter
wherein the cosmetic is a cleansing cream or lotion.
Subclass:
847
![[Patents]](../gifs/ps.gif)
Facial moisturizer:
This subclass is indented under subclass 844. Subject matter
wherein the cosmetic is a facial moisturizer.
Subclass:
848
![[Patents]](../gifs/ps.gif)
Facial astringent:
This subclass is indented under subclass 844. Subject matter
wherein the cosmetic has an astringent effect when applied to
the face.
Subclass:
849
![[Patents]](../gifs/ps.gif)
COUGH AND COLD PREPARATION:
Subject matter involving relief of the symptoms of a cough or
a cold.
Subclass:
850
![[Patents]](../gifs/ps.gif)
Antitussive:
This subclass is indented under subclass 849. Subject matter
involving suppression of coughing.
Subclass:
851
![[Patents]](../gifs/ps.gif)
CYSTIC FIBROSIS:
Subject matter involving the treatment or prevention of
cystic fibrosis.
Subclass:
852
![[Patents]](../gifs/ps.gif)
DANDRUFF:
Subject matter involving the treatment or prevention of
dandruff.
Subclass:
853
![[Patents]](../gifs/ps.gif)
DECONGESTANT:
Subject matter involving a decongestant effect.
Subclass:
854
![[Patents]](../gifs/ps.gif)
Vasoconstrictor:
This subclass is indented under subclass 853. Subject matter
wherein the decongestant is a vasoconstrictor.
Subclass:
855
![[Patents]](../gifs/ps.gif)
Expectorant:
This subclass is indented under subclass 853. Subject matter
wherein the decongestant is an expectorant.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
DERMATITIS:
Subject matter involving the treatment of the skin and
problems related thereto.
Subclass:
858
![[Patents]](../gifs/ps.gif)
Athlete's foot:
Subject matter involving the treatment or prevention of
athlete's foot fungus.
Subclass:
859
![[Patents]](../gifs/ps.gif)
Acne:
Subject matter involving the treatment or prevention of
acne.
Subclass:
860
![[Patents]](../gifs/ps.gif)
Cellulitis:
Subject matter involving the treatment of a cellulitis
condition.
Subclass:
861
![[Patents]](../gifs/ps.gif)
Eczema:
Subject matter involving the treatment of eczema.
Subclass:
862
![[Patents]](../gifs/ps.gif)
Poison (ivy, oak, sumac):
Subject matter involving the treatment or prevention of
poison ivy, poison oak, or poison sumac.
Subclass:
863
![[Patents]](../gifs/ps.gif)
Psoriasis:
Subject matter involving the treatment or prevention of
psoriasis.
Subclass:
864
![[Patents]](../gifs/ps.gif)
Seborrhea:
Subject matter involving the treatment or prevention of
seborrhea.
Subclass:
865
![[Patents]](../gifs/ps.gif)
Diaper rash:
Subject matter involving the treatment or prevention of
diaper rash.
Subclass:
866
![[Patents]](../gifs/ps.gif)
DIABETES:
Subject matter involving the treatment or prevention of
diabetes.
Subclass:
867
![[Patents]](../gifs/ps.gif)
DIARRHEA:
Subject matter involving the treatment or alleviation of the
symptoms of diarrhea in animals.
Subclass:
868
![[Patents]](../gifs/ps.gif)
DISTEMPER:
Subject matter involving the treatment or prevention of
distemper.
Subclass:
869
![[Patents]](../gifs/ps.gif)
DIURETIC:
Subject matter involving substances which yield a diuretic
effect.
Subclass:
870
![[Patents]](../gifs/ps.gif)
EDEMA:
Subject matter involving the treatment or prevention of
edema.
Subclass:
871
![[Patents]](../gifs/ps.gif)
Topical:
This subclass is indented under subclass 870. Subject matter
wherein the treatment of prevention calls for topical
application.
Subclass:
872
![[Patents]](../gifs/ps.gif)
EMESIS (MOTION SICKNESS-NAUSEA):
Subject matter involving the treatment or prevention of
emesis.
Subclass:
873
![[Patents]](../gifs/ps.gif)
EMOLLIENT:
Subject matter involving a specified emollient.
Subclass:
874
![[Patents]](../gifs/ps.gif)
ESTROGENIC AGENT (NONCONTRACEPTIVE):
Subject matter involving a chemical agent used to obtain an
estrogenic effect when administered to a patient.
Subclass:
875
![[Patents]](../gifs/ps.gif)
FLEA CONTROL:
Subject matter involving the control or prevention of fleas.
Subclass:
876
![[Patents]](../gifs/ps.gif)
Collar type:
This subclass is indented under subclass 875. Subject matter
wherein the control and prevention is obtained from a collar
type structure.
Subclass:
877
![[Patents]](../gifs/ps.gif)
GALLSTONE:
Subject matter involving the treatment or prevention of
gallstone.
Subclass:
878
![[Patents]](../gifs/ps.gif)
GERIATRICS:
Subject matter involving the treatment or prevention of
problems associated with aging.
Subclass:
879
![[Patents]](../gifs/ps.gif)
Senility:
This subclass is indented under subclass 878. Subject matter
wherein the problem is senility.
Subclass:
880
![[Patents]](../gifs/ps.gif)
HAIR TREATMENT (THERAPEUTIC-SCALP):
Subject matter involving application to the head or scalp of
a therapeutic composition.
Subclass:
881
![[Patents]](../gifs/ps.gif)
Shampoo:
This subclass is indented under subclass 880. Subject matter
wherein the composition is applied in the form of a shampoo.
Subclass:
882
![[Patents]](../gifs/ps.gif)
HEMORRHOID PREPARATION:
Subject matter involving the treatment or alleviation of
symptoms of hemorrhoids.
Subclass:
883
![[Patents]](../gifs/ps.gif)
HODGKIN'S DISEASE:
Subject matter involving the treatment or prevention of
Hodgkin's disease.
Subclass:
884
![[Patents]](../gifs/ps.gif)
HYPOGLYCEMIA:
Subject matter involving the treatment or prevention of
hypoglycemia.
Subclass:
885
![[Patents]](../gifs/ps.gif)
IMMUNE RESPONSE AFFECTING DRUG:
Subject matter involving the enhancing or reducing of an
immune response in a patient.
Subclass:
886
![[Patents]](../gifs/ps.gif)
INFLAMMATION, SKIN:
Subject matter involving the treatment of skin inflammation.
Subclass:
887
![[Patents]](../gifs/ps.gif)
Topical treatment:
This subclass is indented under subclass 886. Subject matter
wherein application is topically to the skin.
Subclass:
888
![[Patents]](../gifs/ps.gif)
INFLUENZA:
Subject matter involving the treatment or prevention of
influenza.
Subclass:
889
![[Patents]](../gifs/ps.gif)
INTERFERON INDUCER:
Subject matter involving the inducement of the production of
interferon.
Subclass:
890
![[Patents]](../gifs/ps.gif)
IRRITANT (E.G., TEAR GAS, ETC.):
Subject matter involving production of an irritating effect.
Subclass:
891
![[Patents]](../gifs/ps.gif)
KIDNEY STONE:
Subject matter involving the treatment or prevention of
kidney stone.
Subclass:
892
![[Patents]](../gifs/ps.gif)
LAXATIVE:
Subject matter involving the inducement of a laxative effect
in a subject needing said treatment.
Subclass:
893
![[Patents]](../gifs/ps.gif)
LIVER DISORDER:
Subject matter involving the treatment of liver disorder
(excludes cirrhosis of the liver).
Subclass:
894
![[Patents]](../gifs/ps.gif)
Hepatitis:
This subclass is indented under subclass 893. Subject matter
wherein the disorder is hepatitis.
Subclass:
895
![[Patents]](../gifs/ps.gif)
MALARIA:
Subject matter involving the treatment or prevention of
malaria.
Subclass:
896
![[Patents]](../gifs/ps.gif)
MEASLES:
Subject matter involving the treatment or prevention of
measles.
Subclass:
897
![[Patents]](../gifs/ps.gif)
Rubella:
This subclass is indented under subclass 896. Subject matter
wherein the type of measles to be treated is rubella.
Subclass:
898
![[Patents]](../gifs/ps.gif)
MENINGITIS:
Subject matter involving the treatment or prevention of
meningitis.
Subclass:
899
![[Patents]](../gifs/ps.gif)
MENSTRUAL DISORDER:
Subject matter involving the treatment, prevention or
alleviation of symptoms of a menstrual disorder.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
MOUTH TREATMENT:
Subject matter involving the treatment of the mouth.
Subclass:
900
![[Patents]](../gifs/ps.gif)
Periodontitis:
Subject matter under mouth treatment involving the treatment
or prevention of periodontitis.
Subclass:
901
![[Patents]](../gifs/ps.gif)
Mouthwash:
Subject matter under mouth treatment involving the use of a
mouthwash.
Subclass:
902
![[Patents]](../gifs/ps.gif)
Gingival:
Subject matter under mouth treatment involving the treatment
or prevention of disorders of the gingiva.
Subclass:
903
![[Patents]](../gifs/ps.gif)
MULTIPLE SCLEROSIS:
Subject matter involving the treatment, prevention or
alleviation of symptoms of multiple sclerosis.
Subclass:
904
![[Patents]](../gifs/ps.gif)
MULTIPLE VITAMINS:
Subject matter involving a composition which contains two or
more vitamins.
Subclass:
905
![[Patents]](../gifs/ps.gif)
With mineral:
This subclass is indented under subclass 904. Subject matter
wherein the multiple vitamin composition also contains one or
more minerals.
Subclass:
906
![[Patents]](../gifs/ps.gif)
MUSCLE RELAXANT:
Subject matter involving a muscle relaxing effect.
Subclass:
907
![[Patents]](../gifs/ps.gif)
MUSCULAR DYSTROPHY:
Subject matter involving the treatment, prevention or
alleviation of symptoms of muscular dystrophy.
Subclass:
908
![[Patents]](../gifs/ps.gif)
LEUKEMIA:
Subject matter involving the treatment or prevention of
leukemia.
Subclass:
909
![[Patents]](../gifs/ps.gif)
OBESITY:
Subject matter involving the treatment of obesity.
Subclass:
910
![[Patents]](../gifs/ps.gif)
Anorectic:
This subclass is indented under subclass 909. Subject matter
wherein the treatment is a chemical means for reduction or
suppression of appetite.
Subclass:
911
![[Patents]](../gifs/ps.gif)
Bulking agent:
This subclass is indented under subclass 909. Subject matter
wherein a bulking agent is used to reduce food intake.
Subclass:
912
![[Patents]](../gifs/ps.gif)
OPHTHALMIC:
Subject matter involving the treatment of an ophthalmic
disorder.
Subclass:
913
![[Patents]](../gifs/ps.gif)
Glaucoma:
This subclass is indented under subclass 912. Subject matter
wherein the ophthalmic disorder is glaucoma.
Subclass:
914
![[Patents]](../gifs/ps.gif)
Inflammation:
This subclass is indented under subclass 912. Subject matter
wherein the ophthalmic disorder is inflammation.
Subclass:
915
![[Patents]](../gifs/ps.gif)
Wetting agent:
This subclass is indented under subclass 912. Subject matter
wherein a composition acts as a wetting agent or an
artificial tear.
Subclass:
916
![[Patents]](../gifs/ps.gif)
PYRETIC:
Subject matter involving alleviating fever.
Subclass:
917
![[Patents]](../gifs/ps.gif)
RADIOACTIVE, ANTI-:
Subject matter involving the treatment or counter-acting of
the effect of exposure to a radioactive substance or source.
Subclass:
918
![[Patents]](../gifs/ps.gif)
REPELLENT:
Subject matter involving the repelling of a living organism
from any site or locus.
Subclass:
919
![[Patents]](../gifs/ps.gif)
Insect:
This subclass is indented under subclass 918. Subject matter
wherein the organism beign repelled is an insect.
Subclass:
920
![[Patents]](../gifs/ps.gif)
Mammal:
This subclass is indented under subclass 918. Subject matter
wherein the organism being repelled is a mammal.
Subclass:
921
![[Patents]](../gifs/ps.gif)
SHOCK:
Subject matter involving the treatment of shock in a
patient.
Subclass:
922
![[Patents]](../gifs/ps.gif)
SIDE EFFECT REDUCTION BY INCORPORATION OF A SECOND DESIGNATED
INGREDIENT:
Subject matter involving the reducing or eliminating of an
undesirable side effect of a given drug by concurrent
administration of a second designated compound.
Subclass:
923
![[Patents]](../gifs/ps.gif)
SLEEP AID (INSOMNIA):
Subject matter involving inducing sleep.
Subclass:
924
![[Patents]](../gifs/ps.gif)
TUBERCULOSIS:
Subject matter involving the treatment or prevention of
tuberculosis.
Subclass:
925
![[Patents]](../gifs/ps.gif)
ULCER TREATMENT:
Subject matter involving the treatment, alleviation of
symptoms or prevention of an ulcer.
Subclass:
926
![[Patents]](../gifs/ps.gif)
Duodenal:
This subclass is indented under subclass 925. Subject matter
wherein the ulcer is in the duodenal area of the digestive
tract.
Subclass:
927
![[Patents]](../gifs/ps.gif)
Peptic:
This subclass is indented under subclass 925. Subject matter
wherein the ulcer is a peptic ulcer.
Subclass:
928
![[Patents]](../gifs/ps.gif)
Topical:
This subclass is indented under subclass 925. Subject matter
involving topical administration.
Subclass:
929
![[Patents]](../gifs/ps.gif)
VASODILATOR:
Subject matter involving a dilation of the blood vessels on
administration.
Subclass:
930
![[Patents]](../gifs/ps.gif)
VASOCONSTRICTOR (NONDECONGESTANT):
Subject matter involving a constriction of the blood
vessels.
Subclass:
931
![[Patents]](../gifs/ps.gif)
VENEREAL DISEASE:
Subject matter involving treatment, alleviation of symptoms
or prevention of a venereal disease.
Subclass:
932
![[Patents]](../gifs/ps.gif)
Gonorrhea:
This subclass is indented under subclass 931. Subject matter
wherein the venereal disease is gonorrhea.
Subclass:
933
![[Patents]](../gifs/ps.gif)
Syphilis:
This subclass is indented under subclass 931. Subject matter
wherein the venereal disease is syphilis.
Subclass:
934
![[Patents]](../gifs/ps.gif)
Virus:
This subclass is indented under subclass 931. Subject matter
wherein the venereal disease is viral.
Subclass:
935
![[Patents]](../gifs/ps.gif)
UTERINE MOTILITY:
Subject matter involving the increasing of fertility by
increasing uterine motility.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
LIQUID CARRIER, DILUENT OR SOLVENT
Specifically disclosed composition or method where the
inventive concept or point of novelty resides in the carrier
system which is in liquid form. This area of the art
collection also includes those disclosures wherein specified
ingredients are disclosed for the purpose of describing the
carrier system used in combination with an active
ingredient.
Subclass:
936
![[Patents]](../gifs/ps.gif)
DMSO CONTAINING:
Subject matter involving using a composition which contains
dimethyl sulfoxide as a designated nonactive ingredient.
Subclass:
937
![[Patents]](../gifs/ps.gif)
DISPERSION OR EMULSION:
Subject matter involving a composition in the form of a
dispersion or emulsion.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
938
![[Patents]](../gifs/ps.gif)
Oil-water type:
This subclass is indented under subclass 937. Subject matter
wherein the dispersion or emulsion contains both an oil and
water. This subclass covers both oil-in-water and
water-in-oil type emulsions.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
939
![[Patents]](../gifs/ps.gif)
Mineral oil-water type:
This subclass is indented under subclass 938. Subject matter
wherein the oil is mineral oil.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
940
![[Patents]](../gifs/ps.gif)
Quick break type:
This subclass is indented under subclass 939. Subject matter
wherein the mineral oil emulsion is of the quick breaking
type.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
941
![[Patents]](../gifs/ps.gif)
Polyoxyalkylated compound containing:
This subclass is indented under subclass 939. Subject matter
wherein the emulsion contains a polyoxyalkylated compound as
the emulsifying agent.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
942
![[Patents]](../gifs/ps.gif)
Organic sulfonate, sulfate or sulfite containing:
This subclass is indented under subclass 939. Subject matter
wherein the emulsion contains an organic sulfonate, sulfate
or sulfite compound as the emulsifying agent.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
943
![[Patents]](../gifs/ps.gif)
Higher fatty acid or derivative containing:
This subclass is indented under subclass 939. Subject matter
wherein the emulsion contains a higher fatty acid or a
derivative thereof as the emulsifying agent.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 9 for continuous liquid phase colloid systems
(e.g., foams, emulsions, suspensions, dispersions) or agents
for such systems or making or stabilizing such systems or
agents, when generically claimed or when there is no
hierarchically superior provision in the USPC for the
specifically claimed art.
Subclass:
944
![[Patents]](../gifs/ps.gif)
GEL:
Subject matter involving a gel form and containing specified
ingredients to give a gel.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 98 for colloid systems of continuous or
semicontinuous solid phase with discontinuous liquid phase
(gels, pastes, flocs, coagulates) or agents for such systems
or making or stabilizing such systems or agents, when
generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
945
![[Patents]](../gifs/ps.gif)
FOAM:
Subject matter involving a foam and containing specified
ingredients to form said foam.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 10 for foam colloid systems or agents for such
systems or making or stabilizing such systems or agents, when
generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
946
![[Patents]](../gifs/ps.gif)
PENETRANT OR ABSORBENT (ENHANCES PENETRATION INTO SUBJECT
TREATED):
Subject matter involving the increasing or enhancing of the
rate or amount of active ingredient absorbed into the treated
subject. This includes topical application as well as
absorption through the digestive tract.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 198 for wetting agents (e.g., spreading,
penetrating, leveling) or methods of making such agents, when
generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
947
![[Patents]](../gifs/ps.gif)
Topical application:
This subclass is indented under subclass 946. Subject matter
wherein application is to the skin and absorption is through
the skin.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 198 for wetting agents (e.g., spreading,
penetrating, leveling) or methods of making such agents, when
generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
SOLID CARRIER OR SOLID DILUENT
Specifically disclosed composition or method where the
inventive concept or point of novelty resides in the carrier
system which is in the form of a solid. This area of the art
collection also includes those disclosures wherein specified
ingredients are disclosed for the purpose of describing the
carrier system used in combination with an active
ingredient.
Subclass:
948
![[Patents]](../gifs/ps.gif)
SOLID CANDY TYPE:
Subject matter involving an active ingredient in combination
with a candy type base or carrier system.
Subclass:
949
![[Patents]](../gifs/ps.gif)
NATURALLY DERIVED CLAY (E.G., BENTONITE, ETC.):
Subject matter involving the use of a natural clay as a solid
carrier component.
Subclass:
950
![[Patents]](../gifs/ps.gif)
MACROMOLECULAR (OTHER THAN SYNTHETIC RESINS):
Subject matter involving a solid carrier component which is a
high molecular weight polymeric type material.
Subclass:
951
![[Patents]](../gifs/ps.gif)
POWDERS, GRANULES OR PARTICLES OF SPECIFIED MESH OR PARTICLE
SIZE:
Subject matter involving a composition in which an active
ingredient is in combination with a solid carrier in the form
of a powder, granule or particle of specified particle size
or shape.
Subclass:
952
![[Patents]](../gifs/ps.gif)
Wettable:
This subclass is indented under subclass 951. Subject matter
wherein the particles, powder or granules are intended to be
readily mixed with water or other solvent.
Subclass:
953
![[Patents]](../gifs/ps.gif)
SHAPED FORMS ADAPTED FOR NONINGESTIBLE USE OTHER THAN
SUPPOSITORY TYPE (E.G., FILMS, INSERTS, ETC.):
Subject matter involving an active ingredient in combination
with a solid carrier having a designated shape or form.
Subclass:
954
![[Patents]](../gifs/ps.gif)
Ocular:
This subclass is indented under subclass 953. Subject matter
wherein the composition is for application to the eye.
Subclass:
955
![[Patents]](../gifs/ps.gif)
Biodegradable type:
This subclass is indented under subclass 954. Subject matter
wherein the composition is biodegradable within the eye.
Subclass:
956
![[Patents]](../gifs/ps.gif)
Aural or otic (i.e., ear):
This subclass is indented under subclass 953. Subject matter
wherein the composition is for application to the ear.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
GASEOUS OR GAS EMITTING CARRIER OR PROPELLANT
Specifically disclosed composition or method where the
inventive concept or point of novelty resides in the carrier
system which is either gaseous or gas emitting. This area of
the art collection also includes those disclosures wherein
specified ingredients are disclosed for the purpose of
describing the carrier system.
Subclass:
957
![[Patents]](../gifs/ps.gif)
VAPOR EMITTING COMPOSITION:
Subject matter involving application or distribution of an
active ingredient using a vapor or gas.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 1 for continuous gas or vapor phase colloid
system (e.g., smoke, fog, aerosol, cloud, mist) or agents for
such systems or making or stabilizing such systems or agents,
when generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
958
![[Patents]](../gifs/ps.gif)
FOR SMOKING OR INHALING:
Subject matter involving a combination of an active
ingredient with a carrier system which allows administration
by smoking or inhaling.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 1 for continuous gas or vapor phase colloid
system (e.g., smoke, fog, aerosol, cloud, mist) or agents for
such systems or making or stabilizing such systems or agents,
when generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
959
![[Patents]](../gifs/ps.gif)
BREATHING GASES:
Subject matter involving inhalation of a breathing gas such
as oxygen containing gas and supplements thereto.
SEE OR SEARCH CLASS:
516, Colloid Systems and Wetting Agents; Subcombinations
Thereof; Processes of Making, Stabilizing, Breaking, or
Inhibiting, 1 for continuous gas or vapor phase colloid
system (e.g., smoke, fog, aerosol, cloud, mist) or agents for
such systems or making or stabilizing such systems or agents,
when generically claimed or when there is no hierarchically
superior provision in the USPC for the specifically claimed
art.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
PILL, LOZENGE, TABLET OR CAPSULE
Specifically disclosed composition or method where the
inventive concept or point of novelty resides in the carrier
system which takes the form of a pill, lozenge, tablet or
capsule. This area of the art collection also includes those
disclosures wherein specified ingredients are dissolved for
the purpose of describing this form of carrier system used in
combination with an active ingredient.
Subclass:
960
![[Patents]](../gifs/ps.gif)
SIGNIFICANT TABLET FORMULATION (E.G., DESIGNATED EXCIPIENT,
DISINTEGRANT, GLYDENT OR LUBRICANT, ETC.):
Subject matter involving designated nonactive ingredient
which involves in a tableting process.
Subclass:
961
![[Patents]](../gifs/ps.gif)
Binder therefor:
This subclass is indented under subclass 960. Subject matter
wherein the designated ingredient is a binder for the
tableting process.
Subclass:
962
![[Patents]](../gifs/ps.gif)
CAPSULE (E.G., GELATIN, ETC.):
Subject matter involving a capsuling material or
composition.
Subclass:
963
![[Patents]](../gifs/ps.gif)
Microcapsule-sustained of differential release:
This subclass is indented under subclass 962. Subject matter
wherein the capsule is microcapsule and which may allow for
sustained or differential release of the active ingredient
contained therein.
Subclass:
964
![[Patents]](../gifs/ps.gif)
SUSTAINED OR DIFFERENTIAL RELEASE TYPE:
Subject matter involving a combination of an active
ingredient and a carrier system which permits or results in a
sustained or diffeential release of said active ingredient.
Subclass:
965
![[Patents]](../gifs/ps.gif)
Discrete particles in supporting matrix:
This subclass is indented under subclass 964. Subject matter
wherein the combination consists of particles which are
supported or held in a matrix or material for this purpose.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
SUPPOSITORY BOUGIE BASE
Specifically disclosed composition or method of preparation
wherein the composition is in the form of a suppository,
bougy or a base therefor. The group takes only those
references wherein the inventive concept or point of novelty
resides in the make-up of the carrier system rather than the
active ingredient.
Subclass:
966
![[Patents]](../gifs/ps.gif)
RECTAL:
Subject matter involving a form for rectal administration.
Subclass:
967
![[Patents]](../gifs/ps.gif)
VAGINAL:
Subject matter involving a form for vaginal application or
administration.
Subclass:
968
![[Patents]](../gifs/ps.gif)
URETHRAL:
Subject matter involving a form for urethral application or
administration.
Subclass:
969
![[Patents]](../gifs/ps.gif)
OINTMENT OR SALVE BASE:
Subject matter involving a base which is to be combined with
an active ingredient to give an ointment or salve base.
Subclass:
-2
![[Patents]](../gifs/ps.gif)
SPECIAL DESIGNATED INGREDIENT
Specifically disclosed or claimed composition or preparation
which contains, in addition to the active ingredient, at
least one special designated ingredient which has a purpose
or is present other than as a carrier or excipient.
Subclass:
970
![[Patents]](../gifs/ps.gif)
CONTAINING DESIGNATED INGREDIENT TO STABILIZE AN ACTIVE
INGREDIENT:
Subject matter involving a designated ingredient which will
act to stabilize an active ingredient.
Subclass:
971
![[Patents]](../gifs/ps.gif)
Crystallization point depressant or cold stabilizer
containing:
This subclass is indented under subclass 970. Subject matter
wherein said designated ingredient acts to stabilize the
active ingredient from cold or to prevent crystallization of
said active ingredient.
Subclass:
972
![[Patents]](../gifs/ps.gif)
Ultraviolet light stabilizer containing:
This subclass is indented under subclass 970. Subject matter
wherein said designated ingredient acts to stabilize the
active ingredient from the effect of ultraviolet light.
Subclass:
973
![[Patents]](../gifs/ps.gif)
Sulfur compound additive as stabilizer (e.g., sulfites,
etc.):
This subclass is indented under subclass 970. Subject matter
wherein the designated ingredient is a sulfur containing
compound.
Subclass:
974
![[Patents]](../gifs/ps.gif)
CONTAINING DESIGNATED INGREDIENT TO REDUCE NOXIOUS EFFECTS OF
ACTIVE INGREDIENT (E.G., TASTE, MASKING, ODOR REDUCING,
ETC.):
Subject matter involving a designated ingredient which is
intended to reduce the noxious effects of the active
ingredient present.
Subclass:
975
![[Patents]](../gifs/ps.gif)
CHARACTERIZED BY TYHE DESIGNATED SURFACTANT USED:
Subject matter involving a designated ingredient which is to
act as a surfactant.
FOREIGN ART COLLECTIONS
The definitions below correspond to abolished subclasses from
which these collections were formed. See the Foreign Art
Collection schedule of this class for specific
correspondence. {Note: The titles and definitions for
indented art collections include all the details of the
one(s) that are hierarchically superior.
Subclass: FOR 104
Hetero ring is four-membered and includes at least one
nitrogen: Foreign art collection which contains a
heterocyclic ring consisting of four atoms, at least one of
which is nitrogen.
(1) Note. The heterocyclic ring may include other hetero
atoms of the group set forth in the definition of subclass
183 and the relative positions of the hetero atoms may vary.
Subclass: FOR 105
Hetero ring is seven-membered and includes at least one
nitrogen and at least one hetero atom other than nitrogen:
Foreign art collection which contains a heterocyclic ring
consisting of seven atoms, at least one of which is nitrogen
and at least one other hetero atom, other than nitrogen. d
(1) d ( ) Note. See Glossary for definition of het
atom.
Subclass: FOR 106
Hetero ring is seven-membered consisting of one nitrogen and
six carbon atoms: Foreign art collection which contains a
seven-mem heterocyclic ring consisting of six carbon atoms
and one nitrogen atom.
Subclass: FOR 107
Polycyclic ring system having the seven-membered hetero ring
as one of the cyclos: Foreign art collection wherein the
seven-membered hetero ring is one of the cyclos of a
polycyclo ring system.
Subclass: FOR 108
Ring nitrogen is shared by two or three of the cyclos:
Foreign art collection wherein the ring nitrogen of the
seven-membered hetero ring is also a member of one or two
additional cyclos in the polycyclo ring system.
Subclass: FOR 252
1,2- or 1,4-diazine compound having two or more hetero rings:
Subject matter under subclass 247 which is a 1.2- or
1,4-diazine which has a heterocyclic substutuent.
Subclass: FOR 253
Hetero ring other than 1,2- or 1,4-diazine is part of a
polycyclo ring system:
Subject matter wherein the heterocyclic substituent is a part
of a polycyclo substituent.
Subclass: FOR 254
Diazine is bonded directly to the polycyclo ring system:
Subject matter wherein the 1.2- or 1,4-diazine is bonded
directly to the polycyclo system.
Subclass: FOR 255
1,4-Diazines: Subject matter in which the ring nitrogen
occupy the 1, and 4-positions of the diazine nucleus.
Information Products Division -- Contacts
Questions regarding this report should be directed to:
U.S. Patent and Trademark Office
Information Products Division
PK3- Suite 441
Washington, DC 20231
tel: (703) 306-2600
FAX: (703) 306-2737
email: oeip@uspto.gov
Last Modified: 6 October 2000