Class 514 is an integral part of Class 424. It incorporates
all the definitions and rules as to subject matter of Class 424.
SECTION II - 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. SO4
classified on the basis of
R--R
segment only
Example 2 Organic. SO4
or
Organic pesticide. SO4 classified on
the basis of the disclosed organic or organic pesticide material
only.
Example 3. Organic. SO4
or
Amine. SO4
Wherein activity is recited only in the SO4 segment, original
classification is with SO4 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.
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)]n-H or
H-[C(=O)]n-H (n
is 1 or more and wherein the carbon atom bonded to the-[C(=O)]-n 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 (-NO2)
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)]n -C-
(n is 1 or more) and whereinthe carbon atoms
bonded to the-[C(=O)]ngroup
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".
Two typical compounds which would be classified in such a
subclass are:
The following three compounds would also be classified in
such a subclass but they are not typical.
The three atypical examples are considered to meet the title
since there is a chain of atoms between the hetero ring and the
oxygen in which each atom is connected to the hetero ring, the oxygen,
or another atom of the chain by nonionic bonding. The ionic bonding between
the ring nitrogen and the oxygen in the two betaine inner salts
is additional and does not keep the betaines out of such a subclass. However,
a structure, such as
is excluded since no oxygen is attached to the six-membered
hetero ring by nonionic bonding. The oxygen of an N—oxide,
for example,
is considered attached to the ring by nonionic bonding (coordinated
bonding).
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).
An example of the use of this system of nomenclature is as
follows. The compound (Ia)
can also be written as (Ib)
Said compound should also be considered as a (C4N—C4N—C2O)
tricyclo system as in (Ia), rather than as a (C4N—C4
NO—C2O) tricyclo system as possibly
seen in (Ib). The former interpretationis the one with smallest
number of smallest rings that accounts for all atoms and valences.
Some additional illustrative examples of the principle set forth
above are: (II)
Compound II is considered as a bicyclo system composed of
a C2N2O ring and a C4O
ring; it is not considered a diazine
ring for classification. Further, 3—aza—bicyclo [3.1.0] hexane
is classified with pyrrolidines considering the structure
a five-membered ring and a three-membered ring rather than with
piperidines which would require considering it a six-membered ring.
However, see page XI of The Ring Index for an explanation of "valence
bridges".
Similarly, the structure is considered to be a pentacyclo
ring system have three six-membered carbocyclic rings, one five-membered hetero
ring consisting of one ring oxygen and four ring carbons, and one
six-membered ring consisting of one ring nitrogen and five ring carbons.
Betaine inner salts are sometimes shown as ring structures,
etc.,
However, this is not a polycyclo ring system because nonionic
bonding does not exist between the N and O atoms. The bonding between
them is ionic and such as compound is classified as:
Additionally, a structure of the type:
is considered to be a polycyclo ring system composed of five
rings:
C4N—C4O—C4N—C4O—C12N2O2.
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:
A structure such as:
is excluded because the carbon atom shared by two rings is
also shared by a third ring.
The common ring member must be attached to two ring members
of each of the rings by nonionic bonding. Therefore, stuctures such
as:
are also excluded from consideration as "spiro ring
systems" because ionic bonding exists between the hetero
ring atom and an acyclic atom (an oxygen atom in both of these cases) in
the formation of these betaine inner salts. These structures will
be considered and classified as:
TRICYCLO RING SYSTEM
This term denotes a polycyclo ring system which contains
exactly three rings.
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.
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.
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.
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.
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.
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.
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.
Peptide or Protein Sequence,
subclass 260 for peptides or proteins with intrachain cysteine-cysteine
bridges and subclass 270 for other cyclic peptides or proteins.
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.
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.
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.
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.
This subclass is indented under subclass 25. Subject matter wherein an aglycone moiety of the glycoside
contains a cyclopentanohydrophenanthrene nucleus, i.e.,
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.,
This subclass is indented under subclass 28. Subject matter wherein the nonsaccharide hetero ring has
exactly 13 carbon atoms, e.g., erythromycin, 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.
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.,
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.
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.
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.,
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.,
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.,
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.,
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.,
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 NH2 and R" is NH2 or
OH.
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.
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.
(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.
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
subclasses 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.
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.,
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.).
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.
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.
This subclass is indented under subclass 54. Subject matter wherein the polysaccharide consists of repeating
glucose units having the following structure:
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.
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.
This subclass is indented under subclass 23. Subject matter wherein a glucose moiety is substituted with
one or more amino groups, or derivative thereof.
This subclass is indented under subclass 23. Subject matter wherein a glucose moiety is substituted with
one or more amino groups, or derivative thereof.
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.
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.
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.
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.
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.
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.
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.
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.,
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.
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.,
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.,
This subclass is indented under subclass 80. Subject matter in which the organo-phosphorus compound contains
a quinolinyl or isoquinolinyl group, (including hydrogenated).
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.
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.
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.
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.
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.,
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.,
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.,
This subclass is indented under subclass 79. Subject matter in which the organo-phosphorus compound contains
a heterocyclic moiety which has five members.
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.
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.
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.
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.
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.
This subclass is indented under subclass 95. Subject matter in which the organo-phosphorus compound
contains at least two sulfur atoms as ring members.
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.
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.
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.
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.
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.,
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.
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).
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).
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.
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.
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.,
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.,
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.
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.,
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.
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.,
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.,
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.,
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.,
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.,
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.
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.
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
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 .,
This subclass is indented under subclass 75. Subject matter wherein the organo-phosphorus compound contains
at least one nitro substituent bonded to a carbon.
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.,
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.,
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.
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.
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.
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.
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.
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.
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.
for the compound, illustrated below, which is considered
to have only two benzene rings attached to chalcogens which are
bonded directly to phosphorus.
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.
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.
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.
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.
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.
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),
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.
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.
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.
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.
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.
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.
(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.
This subclass is indented under subclass 159. Subject matter wherein an organic nitrogen compound is present
in addition to the salicylic acid compound.
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.
Subject matter under subclass wherein the organic active
ingredient contains a 9, 10-seco-cyclopentanohydrophenanthrene
nucleus, i.e.,
(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.
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.
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.
(1)
Note. Included herein is lanolin as the active ingredient.
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.
This subclass is indented under subclass 169. Subject matter wherein an organic bioactive ingredient is
present in addition to the cyclopentanohydrophenanthrene ring containing compound.
This subclass is indented under subclass 169. Subject matter wherein the cyclopentanohydrophenanthrene
ring containing compound contains a heterocyclic ring. Included
herein are:
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.
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.
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.
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).
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.
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 -CH3 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.
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.
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
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.
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.
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.,
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.
(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.
This subclass is indented under subclass 192. Subject matter wherein the bicyclo heptane ring system contains
two substituents other than hydrogen in 6-position.
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.
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.
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.
This subclass is indented under subclass 197. Subject matter wherein the heterocyclic compound is ampicillin
having the following structure, illustrated below, or salt thereof.
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.
(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.
This subclass is indented under subclass 200. Subject matter wherein the bicyclo octane ring system contains
two substituents other than hydrogen in 7-position.
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.
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.,
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.
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.
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.
Carbon Compounds, Part of the 532-570 Series,
subclasses 950 through 953,for a compound which includes a non-lactam four-membered
hetero ring containing 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.
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,
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:
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,
This subclass is indented under subclass 210.1. 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).
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).
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.
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.
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,
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.
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.
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.
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).
Chemistry, Carbon Compounds, Part of the 532-570
Series,
subclasses 488 through 491for 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.
This subclass is indented under subclass 211.01. Subject matter wherein the seven-membered hetero ring is
bonded directly to a monocyclic cyclopentyl ring
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.
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,
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,
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:
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.
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.
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,
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).
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.
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.
Chemistry, Carbon Compounds, Part of the 530-570
Series,
subclasses 519 through 540for 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.
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.
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.
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.
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,
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.
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.
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:
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
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.
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.
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.
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,
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).
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).
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),
This subclass is indented under subclass 183. Subject matter which contains a seven-membered heterocyclic
ring consisting of two nitrogen and five carbon atoms.
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:
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:
(1)
Note. An example of an active ingredient provided for herein
is:
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.
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:
(1)
Note. An example of an active ingredient provided for herein
is:
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:
(1)
Note. An example of an active ingredient provided for herein
is:
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:
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:
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:
(1)
Note. An example of an ingredient provided for herein is:
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:
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:
(1)
Note. An example of an active ingredient provided for herein
is:
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: