Novel S-Nitrosoglutathione Reductase Inhibitors
AssigneeN30 Pharmaceuticals, Inc.
InventorsXicheng Sun, Jian Qiu
Life of this patent
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Abstract
The present invention is directed to inhibitors of S-nitrosoglutathione reductase (GSNOR), pharmaceutical compositions comprising such GSNOR inhibitors, and methods of making and using the same.
Claims9
A method of treatment of a disease or condition which comprises administering to a patient in need thereof a therapeutically effective amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof
- wherein
- X is selected from the group consisting of O and S;
- Y is selected from the group consisting of O and S;
- Z is selected from the group consisting of Z1, Z2, Z3, and Z4, wherein
- Z1 is
- Z2 is
- Z3 is
- and
- Z4 is
- provided that Z is only Z4 when at least one of X or Y is S;
- R1 is selected from the group consisting of hydrogen, (C1-C6)alkyl, (C3-C7)cycloalkyl, (C1-C6)haloalkyl, unsubstituted aryl(C1-C4)alkyl, substituted aryl(C1-C6)alkyl, (C1-C6)heteroalkyl, substituted or unsubstituted aryl, and substituted or unsubstituted heteroaryl;
- R2 is selected from the group consisting of hydrogen, halogen, cyano, and (C1-C6) alkoxy;
- R3 is selected from the group consisting of hydrogen, halogen, (C1-C6) alkyl, (C1-C6) haloalkyl, (C1-C6) alkoxy, cyano, and N,N-dimethylamino;
- R4 is selected from the group consisting of tetrazole, oxadiazolone, thiadiazolone, methylsulfonylcarbamoyl, and N-hydroxycarbamoyl;
- and
- R5 is selected from the group consisting of carboxy, tetrazole, oxadiazolone, thiadiazolone, methylsulfonylcarbamoyl, and N-hydroxycarbamoyl.
A compound or a pharmaceutically acceptable salt thereof selected from the group consisting of 3-fluoro-4-(7-hydroxy-4-oxo-2-(trifluoromethyl)-4H-chromen-3-yl)benzoic acid, 4-(7-hydroxy-4-oxo-2-(trifluoromethyl)-4H-chromen-3-yl)-3-methylbenzoic acid and 4-(7-hydroxy-4-oxo-2-(trifluoromethyl)-4H-chromen-3-yl)-3-methylbenzoic acid.
Dependencies are inferred from the claim text.