IP Library Granted Patent US 10,016,406
Granted Patent B2
US 10,016,406 · App. 15/681,035 · Granted Jul 10, 2018

Indazole inhibitors of the WNT signal pathway and therapeutic uses thereof

Inventors: John Hood (San Diego, CA); David Mark Wallace (San Diego, CA); Sunil Kumar KC (San Diego, CA)
Assignee: Samumed, LLC
A61K31/4545A61K31/416A61K31/4178A61K31/4184A61K31/437A61K31/44A61K31/444A61K31/4439A61K31/454A61K31/496A61K31/5377A61K31/541A61K31/551C07D231/56C07D401/12C07D401/14C07D403/04C07D403/12C07D403/14C07D405/12C07D409/12C07D471/04C07D487/04C07D487/08
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Quick Facts
Patent No.
US 10,016,406
App. No.
15/681,035
Granted
Jul 10, 2018
Kind
B2
Abstract

Indazole compounds for treating various diseases and pathologies are disclosed. More particularly, the present invention concerns the use of an indazole compound or analogs thereof, in the treatment of disorders characterized by the activation of Wnt pathway signaling (e.g., cancer, abnormal cellular proliferation, angiogenesis, Alzheimer's disease and osteoarthritis), the modulation of cellular events mediated by Wnt pathway signaling, as well as genetic diseases due to mutations in Wnt signaling components. Also provided are methods for treating Wnt-related disease states.

Claims (40)

1. A method of treating a genetic disease caused by mutations in Wnt signaling components, wherein the genetic disease is selected from: polyposis coli , osteoporosis-pseudoglioma syndrome, familial exudative vitreoretinopathy, retinal angiogenesis, early coronary disease, tetra-amelia syndrome, Müllerian-duct regression and virilization, SERKAL syndrome, diabetes mellitus type 2, Fuhrmann syndrome, Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome, odonto-onycho-dermal dysplasia, obesity, split-hand/foot malformation, caudal duplication syndrome, tooth agenesis, Wilms tumor, skeletal dysplasia, focal dermal hypoplasia, autosomal recessive anonychia, neural tube defects, alpha-thalassemia (ATRX) syndrome, fragile X syndrome, ICF syndrome, Angelman syndrome, Prader-Willi syndrome, Beckwith-Wiedemann Syndrome and Rett syndrome in a subject, the method comprising administering to the subject a therapeutically effective amount of a compound of Formula Ia, or a pharmaceutically acceptable salt thereof:

wherein:

R 1 , R 2 , R 4 , R 6 , R 7 , R 8 and R 9 are independently selected from the group consisting of H, C 1-9 alkyl, halide, —CF 3 , —(C 1-9 alkyl) n carbocyclylR 13 , —(C 1-9 alkyl) n heterocyclylR 13 , —(C 1-9 alkyl) n arylR 13 , —(C 1-9 alkyl) n heteroarylR 13 , —(C 1-9 alkyl) n OR 10 , —(C 1-9 alkyl) n SR 10 , —(C 1-9 alkyl) n S(═O)R 11 , —(C 1-9 alkyl) n SO 2 R 10 , —(C 1-9 alkyl) n N(R 10 )SO 2 R 10 , —(C 1-9 alkyl) n SO 2 N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)R 10 , —NO 2 , —CN, —(C 1-9 alkyl) n CO 2 R 10 , and —(C 1-9 alkyl) n C(=A)R 10 ;

R 3 is selected from the group consisting of —NRS(═O)R 14 , —(C 1-9 alkyl)R 14 , -carbocyclylR 14 R 15 , -heterocyclylR 14 R 15 , -arylR 14 R 15 , and -heteroarylR 14 R 15 ;

alternatively, one of each of R 1 and R 2 , R 2 and R 3 , R 3 and R 4 , R 6 and R 7 , R 7 and R 8 or R 8 and R 9 are taken together to form a ring which is selected from the group consisting of aryl, heteroaryl,

wherein each bond represented by a dashed and solid line represents a bond selected from the group consisting of a single bond and a double bond;

each R 10 is independently selected from the group consisting of H, —C 1-9 alkyl, —CF 3 , —(C 1-9 alkyl) n carbocyclyl, —(C 1-9 alkyl) n heterocyclyl, —(C 1-9 alkyl) n aryl, and —(C 1-9 alkyl) n heteroaryl;

each R 11 is independently selected from the group consisting of —C 1-9 alkyl, —CF 3 , —(C 1-9 alkyl) n carbocyclyl, —(C 1-9 alkyl) n heterocyclyl, —(C 1-9 alkyl) n aryl, and —(C 1-9 alkyl) n heteroaryl;

each R 12 is independently selected from the group consisting of —OR 10 and R 10 ;

each R 13 is 1-5 substituents each selected from the group consisting of H, C 1-9 alkyl, halide, —CF 3 , carbocyclyl, heterocyclyl, aryl, heteroaryl, —(C 1-9 alkyl) n OR 10 , —(C 1-9 alkyl) n SR 10 , —(C 1-9 alkyl) n S(═O)R 11 , —(C 1-9 alkyl) n SO 2 R 10 , —(C 1-9 alkyl) n N(R 10 )SO 2 R 10 , —(C 1-9 alkyl) n SO 2 N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)R 10 , —NO 2 , —CN, —(C 1-9 alkyl) n CO 2 R 10 , and —(C 1-9 alkyl) n C(=A)R 10 ;

R 14 is selected from the group consisting of —NR 10 C(=A)R 10 , —NR 10 S(═O)R 11 , —NR 10 SO 2 R 10 , —NR 10 C(═O)N(R 16 ) 2 , —NR 10 C(═S)N(R 10 ) 2 , —NR 10 C(═NR 12 )N(R 10 ) 2 , —N(R 16 ) 2 , —C(═O)NR 10 R 17 , —C(═S)N(R 10 ) 2 , —C(═NR 12 )N(R 10 ) 2 , —OC(=A)R 10 , —C(=A)R 10 , —NR 10 C(=A)OR 10 , and —OC(=A)NR 10 R 10 ;

R 15 is 1-4 substituents each selected from the group consisting of H, C 1-9 alkyl, halide, —CF 3 , carbocyclylR 13 , heterocyclylR 13 , arylR 13 , heteroarylR 13 , —(C 1-9 alkyl) n OR 10 , —(C 1-9 alkyl) n SR 10 , —(C 1-9 alkyl) n S(═O)R 11 , —(C 1-9 alkyl) n SO 2 R 10 , —(C 1-9 alkyl) n N(R 10 )SO 2 R 10 , —(C 1-9 alkyl) n SO 2 N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)R 10 , —NO 2 , —CN, —(C 1-9 alkyl) n CO 2 R 10 , and —(C 1-9 alkyl) n C(=A)R 10 ;

R 16 is —C 1-9 alkyl;

each R 17 is independently selected from the group consisting of -heterocyclylR 13 , —(C 1-9 alkyl)heterocyclylR 13 , and —(C 1-9 alkyl)carbocyclylR 13 ;

R 18 and R 19 are independently selected from the group consisting of H, C 1-9 alkyl, halide, —(C 1-9 alkyl) n carbocyclylR 13 , —(C 1-9 alkyl) n heterocyclylR 13 , —(C 1-9 alkyl) n arylR 13 , —(C 1-9 alkyl) n heteroarylR 13 , —(C 1-9 alkyl) n OR 10 , —(C 1-9 alkyl) n SR 10 , —(C 1-9 alkyl) n S(═O)R 10 , —(C 1-9 alkyl) n SO 2 R 10 , —(C 1-9 alkyl) n N(R 10 )SO 2 R 10 , —(C 1-9 alkyl) n SO 2 N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n C(=A)N(R 10 ) 2 , —(C 1-9 alkyl) n N(R 10 )C(=A)R 10 , —NO 2 , —CN, —(C 1-9 alkyl) n CO 2 R 10 , and —(C 1-9 alkyl) n C(=A)R 10 ;

alternatively, R 18 and R 19 are taken together to form a ring which is selected from the group consisting of benzene and pyridine;

each A is independently selected from O, S, and NR 12 ;

Y 1 , Y 2 , and Y 4 are C;

Y 3 is nitrogen and R 8 is absent; and

each n is 0 or 1.

2. The method of claim 1 , wherein R 1 , R 2 and R 4 are H and R 3 is independently selected from the group consisting of —NRS(═O)R 14 , —(C 1-9 alkyl)R 14 , -carbocyclylR 14 R 15 , -heterocyclylR 14 R 15 , -arylR 14 R 15 and -heteroarylR 14 R 15 .

3. The method of claim 2 , wherein R 3 is -heterocyclylR 14 R 15 .

4. The method of claim 2 , wherein R 3 is -arylR 14 R 15 .

5. The method of claim 2 , wherein R 3 is -heteroarylR 14 R 15 .

6. The method of claim 5 , wherein R 14 is —NR 10 C(=A)R 10 and A is O.

7. The method of claim 5 , in which the heteroaryl is a pyridine.

8. The method of claim 7 , in which R 14 is —NHC(═O)R 10 and R 10 is selected from the group consisting of —C 1-9 alkyl, carbocyclyl, aryl and —(C 1-9 alkyl)aryl.

9. The method of claim 6 , in which R 14 is —C(═O)NHR 17 , R 17 is —(C 1-9 alkyl)carbocyclylR 13 and R 13 is H.

10. The method of claim 1 , wherein R 6 is —(C 1-9 alkyl) n heteroarylR 13 , n is 0 and R 13 is H.

11. The method of claim 1 , wherein R 1 , R 2 , R 4 , R 7 , and R 9 are H; R 3 is heteroarylR 14 R 15 ; and R 6 is —(C 1-9 alkyl) n arylR 13 .

12. The method of claim 11 , in which R 14 is —NHC(═O)R 10 and R 10 is selected from the group consisting of —C 1-9 alkyl, carbocyclyl, aryl and —(C 1-9 alkyl)aryl.

13. The method of claim 12 , wherein R 13 is fluoro.

14. The method of claim 1 , wherein the genetic disease is diabetes mellitus type 2.

15. The method of claim 1 , wherein the genetic disease is obesity.

16. The method of claim 1 , wherein the genetic disease is familial exudative vitreoretinopathy.

17. The method of claim 1 , wherein the genetic disease is retinal angiogenesis.

18. The method of claim 1 , wherein the genetic disease is neural tube defects.

19. The method of claim 1 , wherein the subject is a human.

20. The method of claim 1 , wherein the compound of Formula Ia is selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Mar 12, 2026
From: TMF GROUP NEW YORK, LLC, NOT INDIVIDUALLY BUT SOLELY AS COLLATERAL AGENT
To: BIOSPLICE THERAPEUTICS, INC.
Reel/Frame 075109/0434 →
SECURITY INTEREST Recorded Sep 14, 2022
From: BIOSPLICE THERAPEUTICS, INC.
To: VICKERS VENTURE FUND VI PTE. LTD.; VICKERS VENTURE FUND VI (PLAN) PTE. LTD.; VICKERS-SPLICE CO-INVESTMENT LLC; MED-PATHWAYS II LIMITED
Reel/Frame 061433/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2021
From: SAMUMED, LLC
To: BIOSPLICE THERAPEUTICS, INC.
Reel/Frame 055693/0809 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2018
From: HOOD, JOHN; WALLACE, DAVID MARK; KC, SUNIL KUMAR
To: SAMUMED, LLC
Reel/Frame 045038/0585 →
Continuity (8)
Continuation 15184553 · Jun 16, 2016
Continuation 14741645 · Jun 17, 2015
Continuation 14334005 · Jul 17, 2014
Continuation 13552188 · Jul 18, 2012
Continuation 12852706 · Aug 9, 2010
Provisional Application 61232603 · Aug 10, 2009
Provisional Application 61305459 · Feb 17, 2010
Related Publication 20180153873A1 · Jun 7, 2018