Granted Patent B2

US 8,093,273 · App. 11/255,103 · Granted Jan 10, 2012

Abstract

Claims (103)

1. A method for increasing expression of ApoA-I in a mammal comprising administering a therapeutically effective amount of a compound of Formula I:

wherein:

X is O;

Y is CO;

R 1 , R 3 , R 4 , R 5 , R 6 , R 8 , R 9 , and R 17 are each independently selected from alkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydrogen, hydroxyl, ketone, nitro, phosphate, sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide and thioketone;

R 2 is selected from alkoxy, aryloxy, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydrogen, ketone, nitro, phosphate, sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide and thioketone;

R 7 is selected from alkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, aryl, arylalkyl, carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydroxyl, ketone, nitro, phosphate, sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide and thioketone;

R 10 is selected from alkyl, aryloxy, alkenyl, alkynyl, amide, amino, carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydrogen, hydroxyl, ketone, nitro, phosphate, sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide and thioketone;

each W is independently selected from C and N, wherein if W is N, then p is 0 and if W is C, then p is 1;

at least one W is N;

Z 1 and Z 3 are each a single bond; and

Z 2 is a double bond;

and pharmaceutically acceptable salts and hydrates thereof.

2. The method of claim 1 , wherein the therapeutically effective amount of the compound of Formula I is administered with a pharmaceutically acceptable carrier in a pharmaceutically acceptable composition.

3. The method of claim 1 , further comprising treating a cardiovascular, cholesterol or lipid related disorder.

4. A method for increasing expression of ApoA-I in a mammal comprising administering a therapeutically effective amount of a compound selected from:

5,7-Difluoro-2-(4hydroxyl-phenyl)-chromen-4-one,

2-(3,5-Difluoro-4-hydroxyphenyl)chromen-4-one,

2-(4-Hydroxy-3,5-dimethylphenyl)chromen-4-one,

2-(5-Methoxy-pyridin-2-yl)-chromen-4-one,

2-(5-Hydroxy-pyridin-2-yl)-chromen-4-one,

2-(6-Hydroxy-pyridin-3-yl)-chromen-4-one,

2-(4-Methoxy-phenyl)-thiochromen-4-one,

2-(4-Hydroxy-phenyl)-thiochromen-4-one,

2-(4-Hydroxyphenyl)-3-methyl-4H-chromen-4-one,

4-(6-Bromo-4-oxo-4H-chromen-2-yl)-2-fluorophenyl acetate,

1-(2-Nitro-4-methoxy-phenyl)-chromen-4-one,

2-(4-Hydroxy-2-nitrophenyl)chromen-4-one,

2-(2-Amino-4-methoxy-phenyl)-chromen-4-one,

2-(2-Amino-4-hydroxy-phenyl)-chromen-4-one,

N[5-Hydroxy-2-(4-oxo-4H-chromen-2-yl)-phenyl]acetamide,

6-Hydroxy-2-(4-hydroxymethylphenyl)chromen-4-one,

2-(2-Fluoro-4-hydroxyphenyl)chromen-4-one,

2-(4-Hydroxyphenyl)-8-nitro-4H-chromen-4-one,

2-(4-Hydroxyphenyl)-8-methoxy-4H-chromen-4-one,

2-(4-Hydroxyphenyl)-5,7-dimethoxy-4H-chromen-4-one,

2-(3-Bromo-4-hydroxyphenyl)-4H-chromen-4-one,

2-(4-Hydroxyphenyl)-4-oxo-4H-chromene-6-carbonitrile,

2-(4-Methoxy-phenyl)-chromen-4-one,

2-(3-Fluoro-4-hydroxyphenyl)chromen-4-one,

2-(4-Hydroxyphenyl)-4-oxo-4H-chromene-6-sulfonic acid,

6-Hydroxymethyl-2-(4-hydroxyphenyl)chromen-4-one,

6-((Dimethylamino)methyl)-2-(4-hydrophenyl)-4H-chromen-4-one,

8-Hydroxy-2-(4-hydroxy-phenyl)-chromen-4-one,

2-(4-Hydroxy-phenyl)-chromen-4-one,

7-Hydroxy-2-(4-hydroxy-phenyl)-chromen-4-one,

5-Hydroxy-2-(4-hydroxy-phenyl)-chromen-4-one,

5,7-Djihydroxy-2-(4-hydroxy-phenyl)-chromen-4-one,

5,7-Dihydroxy-2-phenyl-chromen-4-one,

5-Hydroxy-2-phenyl-chromen-4-one,

2-(4-Acetoxy-phenyl)-thiochromen-4-one,

2-(4-Acetoxy-phenyl)-1,1-dioxo-1H-1λ 6 -thiochromen-4-one,

2-(4-Hydroxy-phenyl)-1,1-dioxo-1H-1λ 6 -thiochromen-4-one,

5,7-Dimethoxy-2-(4′-hydroxy-phenyl)-quinolin-4-one,

5,7-Dihydroxy-2-(4-hydroxy-phenyl)-quinolin-4-one,

2-(4-Hydroxy-phenyl)-pyrano[3,2-b]pyridin-4-one,

2-(4-Methoxyphenyl)-4H-pyrano[2,3-b]pyridine-4-one,

2-(4-Hydroxy-phenyl)-pyrano[2,3-b]pyridin-4-one,

2-(4-(2-Hydroxyethoxy)phenyl)-4H-pyrano[2,3-b]pyridine-4-one,

2-(3-Fluoro-4-hydroxyphenyl)pyrano[2,3-b]pyridine-4-one,

2-(4-Hydroxy-3-methylphenyl)-4H-pyrano[2,3-b]pyridine-4-one,

4-(4-Oxo-4H-pyrano[2,3-b]pyridine-2-yl)benzonitrile,

2-(3-Chloro-4-hydroxyphenyl)-4H-pyrano[2,3-b]pyridine-4-one,

2-(3-Bromo-4-hydroxyphenyl)-4H-pyrano[2,3-b]pyridin-4-one,

2-(4-Hydroxy-3-methoxyphenyl)-4H-pyrano[2,3-b]pyridine-4-one,

2-(4-Hydroxy-phenyl)-pyrano[2,3-c]pyridin-4-one,

2-(4-hydroxy-phenyl)-pyrano[3,2-c]pyridin-4-one,

2-(2-(4-Hydroxyphenyl)-4-oxo-4H-chromen-3-yl)acetonitrile,

3-(Hydroxymethyl)-2-(4-hydroxyphenyl)-4H-chromen-4-one,

2-(4-Hydroxyphenyl)-3-(methoxymethyl)-4H-chromen-4-one,

3-(4-Hydroxyphenyl)-2H-isoquinolin-1-one,

3-(3-Fluoro-4-hydroxyphenyl)-5-methoxyisoquinolin-1(2H)-one,

2-Fluoro-4-(5-methoxy-1-(methylamino)-isoquinolin-3-yl)phenol,

4-Naphthalen-2-yl-phenol,

6-Naphthalen-2-yl-pyridin-3-ol,

3-(4-Hydroxyphenyl)-naphthalene-1-ol,

4-lsoquinolin-3-yl-phenol,

4-(1,6-Naphthyridin-7-yl)phenol,

2-(4-Hydroxy-phenyl)-[1,4]naphthoquinone,

4-(Benzo[b][1,4]dioxin-2-yl)phenyl acetate,

4-(Benzo[b][1,4]dioxin-2-yl)phenol,

4-(4H-Chromen-2-yl)-phenol,

2-(4-Hydroxyphenyl)benzo[e][1,3]oxazin-4-one,

6-Naphthalen-2-yl-pyridin-3-ol,

2-(4-Ethoxycarbonyloxy-phenyl)-4-oxo-4H-quinoline-1-carboxylic acid ethyl ester,

Nicotinic acid 4-(4-oxo-4H-chromen-2-yl)-phenyl ester,

Acetic acid 4-(4-oxo-4H-chromen-2-yl)-phenyl ester,

4-(4-oxo-4H-pyrano[2,3-b]pyridine-2-yl)phenyl acetate,

2-Amino-5-guanidino-pentanoic acid 4-(4-oxo-4H-chromen-2-yl)phenyl ester,

4-(Isoquinolin-3-yl)phenyl 2-amino-5-guanidinopentanoate,

4-(1-Oxo-1,2-dihydroisoquinolin-3-yl)phenyl 2-amino-5-guanidinopentanoate, and

2-(4-(Nicotinoyloxy)phenyl)-4-oxo-4H-chromene-5,7-diyl dinicotinate.

5. A method for increasing expression of ApoA-I in a mammal comprising administering a therapeutically effective amount of the compound 4-isoquinolin -3-yl-phenol.

6. A method for increasing expression of ApoA-I in a mammal comprising administering a therapeutically effective amount of a compound of Formula VII:

wherein:

X is O;

Y is CO;

R 1 , R 2 , R 3 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 and R 17 are each independently selected from alkoxy, aryloxy, alkyl, alkenyl, alkynyl, amide, amino, aryl, arylalkyl, carbamate, carboxy, cyano, cycloalkyl, ester, ether, formyl, halogen, haloalkyl, heteroaryl, heterocyclyl, hydrogen, hydroxyl, ketone, nitro, phosphate, sulfide, sulfinyl, sulfonyl, sulfonic acid, sulfonamide and thioketone, or

two adjacent substituents selected from R 1 , R 2 , R 3 , R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are connected in a 5 or 6-membered ring to form a bicyclic aryl or bicyclic heteroaryl;

Z 1 and Z 3 are single bonds, and Z 2 is a double bond;

and pharmaceutically acceptable salts and hydrates thereof.

7. The method of claim 6 , wherein the compound of Formula I is 2-(4-hydroxy-phenyl)-pyrano[2,3-b]pyridin-4-one.

8. The method of claim 6 , further comprising treating a cardiovascular, cholesterol or lipid related disorder.

Assignments (10)