| US 7,452,887 B2 | ||
| Quinoline- and isoquinoline-based compounds exhibiting ATP-utilizing enzyme inhibitory activity, and compositions, and uses thereof | ||
| John K. Dickson, Jr., Apex, N.C. (US); Kevin P. Williams, Chapel Hill, N.C. (US); and Carl Nicholas Hodge, Los Gatos, Calif. (US) | ||
| Assigned to Amphora Discovery Corporation, Durham, N.C. (US) | ||
| Filed on Jun. 03, 2005, as Appl. No. 11/145,562. | ||
| Claims priority of provisional application 60/577224, filed on Jun. 04, 2004. | ||
| Prior Publication US 2006/0009460 A1, Jan. 12, 2006 | ||
| Int. Cl. A61K 31/496 (2006.01); A61K 31/4709 (2006.01); C07D 401/10 (2006.01) | ||
| U.S. Cl. 514—253.06 [514/310; 514/313; 544/363; 546/143; 546/160] | 42 Claims |
1. A compound or Formula 1 or a
![]() Ar is chosen from aryl, substituted aryl, heteroaryl, and substituted heteroaryl;
A is —N— and B is —CH—, or A is —CH— and B is —N—;
L is chosen from NR1 and O;
R1 is chosen from H, alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, heterocycloalkyl, and substituted heterocycloalkyl;
X and Y are independently chosen from CH and N;
G is chosen from a covalent bond and NR6;
R6 is chosen from hydrogen and optionally substituted alkyl; and
R is chosen from optionally substituted heterocycloalkyl, with the proviso that when Ar is phenyl, A is —N—, B is —CH—, L is NR1, R1 is H, X is CH,
Y is CH, and G is a covalent bond, then R is not 4-methylpiperazin-1-yl.
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