IP Library Granted Patent US 10,245,259
Granted Patent B2
US 10,245,259 · App. 16/008,838 · Granted Apr 2, 2019

Methods of treating RBP4 related diseases with triazolopyridines

Inventors: Yu-Hsin Tom Lin (San Diego, CA); Cheng-Chi Irene Wang (San Diego, CA)
Assignee: Belite Bio, Inc
A61K31/4545A61K9/0019A61K9/0053A61K31/4985A61K31/519A61K31/5365A61K31/5383A61P3/04A61P3/10
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Quick Facts
Patent No.
US 10,245,259
App. No.
16/008,838
Granted
Apr 2, 2019
Kind
B2
Abstract

Provided herein are heterocyclic derivative compounds and pharmaceutical compositions comprising said compounds that are useful for the treatment of retinal binding protein (RBP4) related diseases, such as obesity and the like.

Claims (60)

1. A method of treating a metabolic disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof

wherein:

each R 1 is independently halogen, haloalkyl, or alkyl;

R 2 is —H, —OH, or halogen;

p is 0, 1, 2, 3, 4, or 5; and

A has the structure:

wherein:

α, β, χ, and δ are each independently absent or present, and when present each is a bond;

X is N;

Z 1 is S, O, or N;

Z 2 is S, O, N, or NR 3 ;

R 3 is H, C 1 -C 4 alkyl, or oxetane; and

B is a substituted or unsubstituted fused 5-, 6-, or 7-membered ring structure; and

wherein the metabolic disease or disorder is non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH).

2. The method of claim 1 , wherein:

when α is present, then Z 1 and Z 2 are N, X is N, β is present, and χ and δ are absent.

3. The method of claim 1 , wherein A has the structure

wherein

n is 0, 1, or 2;

α, β, χ, δ, ε, and ϕ are each independently absent or present, and when present each is a bond;

Z 1 is S, O, or N;

Z 2 is S, O, N or NR 3 ,

wherein R 3 is H, C 1 -C 4 alkyl, or oxetane;

X is N;

Y 1 , Y 2 , Y 3 and each occurrence of Y 4 are each independently CR 4 , C(R 5 ) 2 , NR 6 , O, N, SO 2 , or —(C═O)—, wherein:

each R 4 is independently H, halogen, C 1 -C 10 alkyl, C 1 -C 10 cycloalkyl, —O(C 1 -C 10 alkyl), —C(O)OH, —C(O)O(C 1 -C 10 alkyl), —C(O)NH 2 , —C(O)NH (C 1 -C 4 alkyl), —C(O)N(C 1 -C 4 alkyl) 2 , —NHC(O)NH(C 1 -C 10 alkyl), —NHC(O)N(C 1 -C 4 alkyl) 2 , —SO 2 NH(C 1 -C 10 alkyl), —SO 2 N(C 1 -C 10 alkyl) 2 , —CN, or —CF 3 ;

each R 5 is independently H or C 1 -C 10 alkyl; and

each R 6 is independently H, C 1 -C 10 alkyl, C 3 -C 6 cycloalkyl, —(C 1 -C 10 alkyl)CF 3 , —(C 1 -C 10 alkyl)OCH 3 , —(C 1 -C 10 alkyl)-halogen, —SO 2 (C 1 -C 10 alkyl), —SO 2 (C 1 -C 10 alkyl)-CF 3 , —SO 2 (C 1 -C 10 alkyl)OCH 3 , —SO 2 (C 1 -C 10 alkyl)-halogen, —C(O)(C 1 -C 10 alkyl), —C(O)(C 1 -C 10 alkyl)CF 3 , —C(O)(C 1 -C 10 alkyl)OCH 3 , —C(O)(C 1 -C 10 alkyl)-halogen, —C(O)NH(C 1 -C 10 alkyl), —C(O)N(C 1 -C 10 alkyl) 2 , —(C 1 -C 10 alkyl)C(O)OH, —C(O)NH 2 , or oxetane.

4. The method of claim 1 , wherein:

when α is present, then Z 1 and Z 2 are N, X is N, β is present, and χ and δ are absent;

when ε and ϕ are each present, then n=1, and each of Y 1 , Y 2 , Y 3 , and Y 4 , are independently —CR 4 — or N; or

when ε and ϕ are each absent, then n=0, 1 or 2, each of Y 1 , Y 2 , Y 3 , and each occurrence of Y 4 are independently C(R 5 ) 2 , NR 6 , O, or SO 2 .

5. The method of claim 1 , wherein:

α, β, ε, and ϕ are present;

χ and δ are absent;

Z 1 is N;

Z 2 is N; and

X is N.

6. The method of claim 1 , wherein A has the structure:

wherein:

Y 1 , Y 2 , Y 3 and Y 4 are each independently CR 4 or N; and

each R 4 is independently H, halogen, C 1 -C 10 alkyl, C 1 -C 10 cycloalkyl, —O(C 1 -C 10 alkyl), —C(O)OH, —C(O)O(C 1 -C 10 alkyl), —C(O)NH 2 , —C(O)NH (C 1 -C 4 alkyl), —C(O)N(C 1 -C 4 alkyl) 2 , —NHC(O)NH(C 1 -C 10 alkyl), —NHC(O)N(C 1 -C 4 alkyl) 2 , —SO 2 NH(C 1 -C 10 alkyl), —SO 2 N(C 1 -C 10 alkyl) 2 , —CN, or —CF 3 .

7. The method of claim 1 , wherein A has the structure

wherein:

each R 4 is independently H, halogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, —O(C 1 -C 4 alkyl), —CN, —CF 3 , —C(O)OH, —C(O)NH 2 , —C(O)N(CH 3 ) 2 , —C(O)NHCH 3 , or —NHC(O)N(CH 3 ) 2 .

8. The method of claim 1 , wherein each R 1 is independently F, Br, Cl, C 1-6 haloalkyl, or C 1-6 alkyl.

9. The method of claim 1 , wherein each R 1 is independently F or CF 3 .

10. A method of treating a metabolic disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a therapeutically effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof; and

wherein the metabolic disease or disorder is non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH).

11. A method of treating a metabolic disease or disorder in a subject in need thereof, the method comprising administering to the subject a composition comprising a therapeutically effective amount of a compound having the structure:

or a pharmaceutically acceptable salt thereof; and

wherein the metabolic disease or disorder is non-alcoholic fatty liver disease (NAFLD) or non-alcoholic steatohepatitis (NASH).

12. The method of claim 1 , wherein the metabolic disease or disorder is non-alcoholic fatty liver disease (NAFLD).

13. The method of claim 1 , wherein the therapeutically effective amount of a compound of Formula (I), or a pharmaceutically acceptable salt thereof is up to 25 mg per day, up to 50 mg per day, up to 75 mg per day, up to 100 mg per day, up to 150 mg per day, up to 200 mg per day, up to 400 mg per day, up to 600 mg per day, up to 800 mg per day, or up to 1000 mg per day.

14. The method of claim 1 , wherein 24 hours after administration of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, the serum or plasma levels of RBP4 are reduced by at least 50% from baseline.

15. The method of claim 1 , wherein 24 hours after administration of a compound of Formula (I), or a pharmaceutically acceptable salt thereof, the serum or plasma levels of RBP4 are reduced by at least 1 mg/dL.

16. The method of claim 1 , wherein the disease or disorder is non-alcoholic steatohepatitis (NASH).

17. The method of claim 1 , wherein the compound is administered to the subject orally or intravenously.

18. The method of claim 1 , wherein the administration is to treat an existing disease or disorder.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2023
From: PETRUKHIN, KONSTANTIN
To: THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK
Reel/Frame 063420/0831 →
CONFIRMATORY LICENSE Recorded Feb 7, 2023
From: COLUMBIA UNIV NEW YORK MORNINGSIDE
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 062667/0427 →
CHANGE OF NAME Recorded Nov 9, 2018
From: LIN BIOSCIENCE CO., LTD.
To: BELITE BIO, INC
Reel/Frame 047497/0619 →
CORRECTIVE ASSIGNMENT TO CORRECT THE PROPERTY NUMBERS PREVIOUSLY RECORDED AT REEL: 0460413 FRAME: 0038. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 17, 2018
From: LIN BIOSCIENCE HOLDINGS CORPORATION
To: LIN BIOSCIENCE CO., LTD.
Reel/Frame 046896/0672 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 20, 2018
From: LIN BIOSCIENCE HOLDINGS CORPORATION
To: LIN BIOSCIENCE CO., LTD.
Reel/Frame 046413/0038 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2018
From: LIN, YU-HSIN TOM; WANG, CHENG-CHI IRENE
To: LIN BIOSCIENCE HOLDINGS CORPORATION
Reel/Frame 046521/0602 →
Continuity (1)
Related Publication 20180360818A1 · Dec 20, 2018
Cited By (2)
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