IP Library Patent Application 14349014
Patent Application
App. No. 14/349,014

SUBSTITUTED AMINOTHIAZOLES AS INHIBITORS OF CANCERS, INCLUDING HEPATOCELLULAR CARCINOMA, AND AS INHIBITORS OF HEPATITIS VIRUS REPLICATION

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Patent No.
US None
App. No.
14/349,014
Abstract

Pharmaceutical compositions of the invention are presented which comprise substituted aminothiazoles derivatives. The substituted aminothiazoles derivatives have a disease-modifying action in the treatment of diseases associated with unregulated cell growth. Such diseases include cancers such as hepatocellular carcinoma, and viral infections from a hepatitis virus.

Claims (227)

1 . A compound having formula (I):

Including hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, wherein:

R 1 is selected from the group consisting of hydrogen, C 1 -C 9 linear alkyl, isopropyl, cyclohexyl, bromine, cyano,

R 2 is selected from the group consisting of hydrogen, methyl, isopropyl, tert-butyl, benzyl, and

Ar 1 is selected from the group consisting of phenyl,

Ar 2 is selected from the group consisting of phenyl,

wherein compounds of the structures

are excluded from the compounds of formula (I).

2 . (canceled)

3 . (canceled)

4 . (canceled)

5 . (canceled)

6 . The compound according to claim 1 , which is:

4-(pyridin-2-yl)-n-(pyrimidin-4-yl)thiazol-2-amine;

4-(6-bromopyridin-2-yl)-n-(pyrimidin-2-yl)thiazol-2-amine;

4-(4-methylpyridin-2-yl)-n-(pyrimidin-2-yl)thiazol-2-amine;

4-(3,5-dimethylpyridin-2-yl)-n-(pyrimidin-2-yl)thiazol-2-amine;

6-(2-(pyrimidin-2-ylamino)thiazol-4-yl)pyridin-2-ol;

N-(pyrimidin-2-yl)-4-(quinolin-2-yl)thiazol-2-amine;

N-(5-chloropyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(5-bromopyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(4-methylpyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine:

4-(pyridin-2-yl)-N-(4-(trifluoromethyl)pyrimidin-2-yl)thiazol-2-amine;

6-methyl-N-(4-(pyridin-2-yl)thiazol-2-yl)benzo[d]thiazol- 2 -amine;

5-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-ethyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-pentyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-cyclohexyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-nonyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-benzyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

2-((4-(pyridin-2-yl)thiazol-2-yl)(pyrimidin-2-yl)amino)ethanol;

5-bromo-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methanol;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl acetate;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl butyrate;

Ethyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(4-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate ;

ethyl 4-(6-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate ;

ethyl 2-((4-methylpyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5-carboxylate ;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylic acid;

methyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

tert-butyl 2-(tert-butyl(pyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5-carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-methyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide

N-benzyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

24-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino) benzamido)-1,21-dioxo-1-(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)-5,8,11,14,17-pentaoxa-2,20-diazapentacosan-25-oic acid;

N-(31-oxo-35-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)-3, 6, 9, 12, 15, 18, 21, 24, 27-nonaoxa-30-azapentatriacontyl)-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino) thiazole-5-carboxamide;

4-Pyridin-2-yl-2-(pyrimidin-2-ylamino)-thiazole-5-carbonitrile;

and pharmaceutically acceptable forms thereof.

7 . A composition comprising an effective amount of at least one compound according to claim 1 .

8 . A composition according to claim 7 , further comprising at least one excipient.

9 . A composition according to claim 8 , wherein the at least one compound is at least one member selected from the group consisting of:

4-(pyridin-2-yl)-N-(pyrimidin-4-yl)thiazol-2-amine;

4-(6-bromopyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(4-methylpyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(3,5-dimethylpyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

6-(2-(pyrimidin-2-ylamino)thiazol-4-yl)pyridin-2-ol;

N-(pyrimidin-2-yl)-4-(quinolin-2-yl)thiazol-2-amine;

N-(5-chloropyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(5-bromopyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(4-methylpyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine:

4-(pyridin-2-yl)-N-(4-(trifluoromethyl)pyrimidin-2-yl)thiazol-2-amine;

6-methyl-N-(4-(pyridin-2-yl)thiazol-2-yl)benzo[d]thiazol-2-amine;

5-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-ethyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-pentyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-cyclohexyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-nonyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-benzyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

2-((4-(pyridin-2-yl)thiazol-2-yl)(pyrimidin-2-yl)amino)ethanol;

5-bromo-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methanol;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl acetate;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl butyrate;

Ethyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(4-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(6-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 2-((4-methylpyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5 -carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylic acid;

Methyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

tert-butyl 2-(tert-butyl(pyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5-carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-methyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-benzyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

24-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)-1,21-dioxo-1-(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)-5,8,11,14,17-pentaoxa-2,20-diazapentacosan-25-oic acid;

N-(31-oxo-35-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3, 4-d]imidazol-4-yl)-3, 6, 9, 12, 15, 18, 21, 24, 27-nonaoxa-30-azapentatriacontyl)-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino) thiazole-5-carboxamide;

4-Pyridin-2-yl-2-(pyrimidin-2-ylamino)-thiazole-5-carbonitrile and pharmaceutically acceptable forms thereof.

10 . (canceled)

11 . A method for treating a disease associated with unregulated cell growth, said method comprising administering to a subject an effective amount of at least one compound of the formula (I),

including hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, to treat the disease wherein:

R 1 is selected from the group consisting of hydrogen, C 1 -C 9 linear alkyl, isopropyl, cyclohexyl, bromine, cyano,

R 2 is selected from the group consisting of hydrogen, methyl, isopropyl, tert-butyl, benzyl, and

Ar 1 is selected from the group consisting of phenyl,

Ar 2 is selected from the group consisting of phenyl,

12 . (canceled)

13 . The method of claim 11 , wherein the at least one compound is administered in a composition further comprising at least one excipient.

14 . The method of claim 13 , wherein the at least one compound is at least one member selected from the group consisting of

4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N,4-diphenylthiazol-2-amine;

N-phenyl-4-(pyridin-2-yl)thiazol-2-amine;

4-phenyl-N-(pyrimidin-2-yl)thiazol-2-amine;

N,4-di(pyridin-2-yl)thiazol-2-amine;

4-(pyridin-3-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(pyridin-4-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-(pyrazin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

4-(pyridin-2-yl)-N-(pyrimidin-4-yl)thiazol-2-amine;

4-(6-bromopyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(4-methylpyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(3,5-dimethylpyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

6-(2-(pyrimidin-2-ylamino)thiazol-4-yl)pyridin-2-ol;

N-(pyrimidin-2-yl)-4-(quinolin-2-yl)thiazol-2-amine;

N-(5-chloropyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(5-bromopyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(4-methylpyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine:

4-(pyridin-2-yl)-N-(4-(trifluoromethyl)pyrimidin-2-yl)thiazol-2-amine;

6-methyl-N-(4-(pyridin-2-yl)thiazol-2-yl)benzo[d]thiazol- 2 -amine;

5-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-ethyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-pentyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-cyclohexyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-nonyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-benzyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

2-((4-(pyridin-2-yl)thiazol-2-yl)(pyrimidin-2-yl)amino)ethanol;

5-bromo-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methanol;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl acetate;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl butyrate;

Ethyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(4-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(6-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 2-((4-methylpyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5-carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylic acid;

Methyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

tert-butyl 2-(tert-butyl(pyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5-carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-methyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-benzyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

24-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino)benzamido)-1,21-dioxo-1-(4- (pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)-5,8,11,14,17-pentaoxa-2,20- diazapentacosan-25-oic acid;

N-(31-oxo-35-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3, 4-d]imidazol-4-yl)-3, 6, 9, 12, 15, 18, 21, 24, 27-nonaoxa-30-azapentatriacontyl)-4-(pyridin-2-yl)-2-(pyrimidin-2- ylamino) thiazole-5-carboxamide;

4-Pyridin-2-yl-2-(pyrimidin-2-ylamino)-thiazole-5-carbonitrile;

3-(4-Phenyl-thiazol-2-ylamino)-phenol;

(3-Chloro-2-methyl-phenyl)-(4-pyridin-2-yl-thiazol-2-yl)-amine;

and pharmaceutically acceptable forms thereof.

15 . The method of claim 11 , wherein the disease associated with unregulated cell growth is a cancer selected from the group consisting of hepatocellular carcinoma, primary liver cancer, hepatoblastoma, breast cancer, ovarian cancer, lung cancer, leukemia and cholangiocarcinoma.

16 . (canceled)

17 . (canceled)

18 . (canceled)

19 . (canceled)

20 . (canceled)

21 . (canceled)

22 . (canceled)

23 . (canceled)

24 . The method of claim 11 , wherein the disease associated with unregulated cell growth is metastatic disease.

25 . A method for treating a disease associated with infection of the liver with a virus, said method comprising administering to a subject an effective amount of at least one compound of the formula (I),

including hydrates, solvates, pharmaceutically acceptable salts, prodrugs and complexes thereof, to treat the disease wherein:

R 1 is selected from the group consisting of hydrogen, C 1 -C 9 linear alkyl, isopropyl, cyclohexyl, bromine, cyano,

R 2 is selected from the group consisting of hydrogen, methyl, isopropyl, tert-butyl, benzyl, and

Ar 1 is selected from the group consisting of phenyl,

Ar 2 is selected from the group consisting of phenyl,

26 . (canceled)

27 . The method of claim 25 , wherein the at least one compound is administered in a composition further comprising at least one excipient.

28 . The method of claim 27 , wherein the at least one compound is at least one member selected from the group consisting of

4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N,4-diphenylthiazol-2-amine;

N-phenyl-4-(pyridin-2-yl)thiazol-2-amine;

4-phenyl-N-(pyrimidin-2-yl)thiazol-2-amine;

N,4-di(pyridin-2-yl)thiazol-2-amine;

4-(pyridin-3-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(pyridin-4-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-(pyrazin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

4-(pyridin-2-yl)-N-(pyrimidin-4-yl)thiazol-2-amine;

4-(6-bromopyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(4-methylpyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

4-(3,5-dimethylpyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

6-(2-(pyrimidin-2-ylamino)thiazol-4-yl)pyridin-2-ol;

N-(pyrimidin-2-yl)-4-(quinolin-2-yl)thiazol-2-amine;

N-(5-chloropyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(5-bromopyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine;

N-(4-methylpyrimidin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine:

4-(pyridin-2-yl)-N-(4-(trifluoromethyl)pyrimidin-2-yl)thiazol-2-amine;

6-methyl-N-(4-(pyridin-2-yl)thiazol-2-yl)benzo[d]thiazol-2-amine;

5-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-ethyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-pentyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-cyclohexyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

5-nonyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-isopropyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-methyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

N-benzyl-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

2-((4-(pyridin-2-yl)thiazol-2-yl)(pyrimidin-2-yl)amino)ethanol;

5-bromo-4-(pyridin-2-yl)-N-(pyrimidin-2-yl)thiazol-2-amine;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methanol;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl acetate;

(4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)methyl butyrate;

Ethyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(4-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 4-(6-methylpyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

Ethyl 2-((4-methylpyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5 -carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylic acid;

Methyl 4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxylate;

tert-butyl 2-(tert-butyl(pyrimidin-2-yl)amino)-4-(pyridin-2-yl)thiazole-5-carboxylate;

4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-methyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

N-benzyl-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazole-5-carboxamide;

24-(4-(((2,4-diaminopteridin-6-yl)methyl)(methyl)amino) benzamido)-1,21-dioxo-1-(4- (pyridin-2-yl)-2-(pyrimidin-2-ylamino)thiazol-5-yl)-5,8,11,14,17-pentaoxa-2,20-diazapentacosan-25-oic acid;

N-(31-oxo-35-((3as,4s,6aR)-2-oxohexahydro-1H-thieno[3, 4-d]imidazol-4-yl)-3, 6, 9, 12, 15, 18, 21, 24, 27-nonaoxa-30-azapentatriacontyl)-4-(pyridin-2-yl)-2-(pyrimidin-2-ylamino) thiazole-5-carboxamide;

4-pyridin-2-yl-2-(pyrimidin-2-ylamino)-thiazole-5-carbonitrile;

3-(4-phenyl-thiazol-2-ylamino)-phenol;

(3-chloro-2-methyl-phenyl)-(4-pyridin-2-yl-thiazol-2-yl)-amine;

and pharmaceutically acceptable forms thereof.

29 . The method of claim 25 , wherein the virus is a hepatitis virus.

30 . The method of claim 25 , wherein the hepatitis virus is the hepatits A virus.

31 . The method of claim 25 , wherein the hepatitis virus is the hepatits B virus.

32 . The method of claim 25 , wherein the hepatitis virus is the hepatits C virus.

33 . The method of claim 25 , wherein the hepatitis virus is the hepatits D virus.

34 . The method of claim 25 , wherein the hepatitis virus is the hepatits E virus.

35 . The method of claim 25 , wherein the virus is any virus infecting the liver

Assignments (4)
MERGER Recorded Mar 9, 2015
From: PHILADELPHIA HEALTH & EDUCATION CORPORATION D/B/A DREXEL UNIVERSITY COLLEGE OF MEDICINE
To: DREXEL UNIVERSITY
Reel/Frame 035114/0990 →
CHANGE OF NAME Recorded Mar 9, 2015
From: INSTITUTE FOR HEPATITIS AND VIRUS RESEARCH
To: BARUCH S. BLUMBERG INSTITUTE
Reel/Frame 035146/0844 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2014
From: CUCONATI, ANDREA; XU, XIAODONG
To: INSTITUTE FOR HEPATITIS AND VIRUS RESEARCH
Reel/Frame 032637/0555 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 9, 2014
From: BLOCK, TIMOTHY
To: PHILADELPHIA HEALTH & EDUCATION CORPORATION D/B/A DREXEL UNIVERSITY COLLEGE OF MEDICINE
Reel/Frame 032637/0660 →