IP Library Granted Patent US 11,040,998
Granted Patent B2
US 11,040,998 · App. 16/593,262 · Granted Jun 22, 2021

Bile acid derivatives as FXR/TGR5 agonists and methods of use thereof

Inventors: Guoqiang Wang (Belmont, MA); Yat Sun Or (Waltham, MA); Ruichao Shen (Belmont, MA); Xuechao Xing (Wilmington, MA); Jiang Long (Wayland, MA); Peng Dai (Auburndale, MA); Brett Granger (Sudbury, MA); Jing He (Somerville, MA)
Assignee: ENANTA PHARMACEUTICALS, INC.
C07J43/003C07J41/005C07J41/0055C07J41/0088C07J9/00C07J9/005C07J51/00
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Quick Facts
Patent No.
US 11,040,998
App. No.
16/593,262
Granted
Jun 22, 2021
Kind
B2
Abstract

The present invention provides compounds represented by Formula I, or pharmaceutically acceptable salts, stereoisomers, solvates, hydrates or combination thereof, The invention also provides pharmaceutical compositions comprising these compounds and methods of using this compounds for treating FXR-mediated or TGR5-mediated diseases or conditions.

Claims (73)

1. A compound represented by Formula (III-10) or a pharmaceutically acceptable salt thereof:

wherein:

R 1 is selected from the group consisting of:

1) Halogen;

2) Hydroxyl;

3) Substituted or unsubstituted —C 1 -C 8 alkyl;

4) Substituted or unsubstituted —C 2 -C 8 alkenyl;

5) Substituted or unsubstituted —C 2 -C 8 alkynyl;

6) Substituted or unsubstituted —C 3 -C 8 cycloalkyl;

7) Substituted or unsubstituted aryl;

8) Substituted or unsubstituted arylalkyl;

9) Substituted or unsubstituted heterocycloalkyl;

10) Substituted or unsubstituted heteroaryl;

11) Substituted or unsubstituted heteroarylalkyl; and

12)—NR 10 R 11 ;

R 2 is selected from the group consisting of:

1) Hydrogen;

2) Substituted or unsubstituted —C 1 -C 8 alkyl;

3) Substituted or unsubstituted —C 2 -C 8 alkenyl;

4) Substituted or unsubstituted —C 2 -C 8 alkynyl;

5) Substituted or unsubstituted arylalkyl; and

6) Substituted or unsubstituted aryl;

R c is selected from the group consisting of:

1) Hydrogen;

2) Substituted or unsubstituted —C 1 -C 8 alkyl;

3) Substituted or unsubstituted —C 2 -C 8 alkenyl;

4) Substituted or unsubstituted —C 2 -C 8 alkynyl;

5) Substituted or unsubstituted arylalkyl; and

6) Substituted or unsubstituted aryl;

m is selected from 0, 1, 2 and 3;

R 7 is selected from the group consisting of:

1) Hydrogen;

2) Halogen;

3) Substituted or unsubstituted —C 1 -C 8 alkyl;

4) Substituted or unsubstituted —C 2 -C 8 alkenyl;

5) Substituted or unsubstituted —C 2 -C 8 alkynyl; and

6) Substituted or unsubstituted —C 3 -C 8 cycloalkyl; and

R 10 and R 11 are each independently selected from hydrogen, substituted or unsubstituted —C 1 -C 8 alkyl, substituted or unsubstituted —C 2 -C 8 alkenyl, substituted or unsubstituted-C 2 -C 8 alkynyl, substituted or unsubstituted —C 3 -C 8 cycloalkyl, or R 10 and R 11 are taken together with the nitrogen atom to which they are attached to form a heterocyclic ring.

2. A method for treating a disease or condition selected from the group consisting of primary biliary cirrhosis, cerebrotendinous xanthomatosis, primary sclerosing cholangitis, alcoholic liver disease, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, atherosclerosis, hypercholesterolemia, hypertriglyceridemia, Type II diabetes, and hepatocellular carcinoma in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 1 .

3. The method according to claim 2 , wherein the disease or condition is selected from the group consisting of primary biliary cirrhosis, nonalcoholic fatty liver disease, and nonalcoholic steatohepatitis.

4. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically acceptable carrier.

5. The compound of claim 1 , wherein R 2 and R c are both hydrogen, R 7 is ethyl, and m is 0 or 1.

6. The compound of claim 1 , selected from the compounds set forth in the table below:

Compound

Structure

 4

 6

10

14

15

30

44-b

79

or a pharmaceutically acceptable salt thereof.

7. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

8. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

9. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

10. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

11. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

12. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

13. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

14. The compound of claim 6 , having the structure

or a pharmaceutically acceptable salt thereof.

15. A method for treating a disease or condition selected from the group consisting of primary biliary cirrhosis, cerebrotendinous xanthomatosis, primary sclerosing cholangitis, alcoholic liver disease, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, atherosclerosis, hypercholesterolemia, hypertriglyceridemia, Type II diabetes, and hepatocellular carcinoma in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a compound of claim 6 .

16. The method according to claim 15 , wherein the disease or condition is selected from the group consisting of primary biliary cirrhosis, nonalcoholic fatty liver disease, and nonalcoholic steatohepatitis.

17. A pharmaceutical composition comprising a compound according to claim 6 and a pharmaceutically acceptable excipient or carrier.

Continuity (4)
Continuation 15085800 · Mar 30, 2016
Provisional Application 62140927 · Mar 31, 2015
Provisional Application 62287267 · Jan 26, 2016
Related Publication 20200109164A1 · Apr 9, 2020
Cited By (1)
US 12,281,140