IP Library Granted Patent US 10,351,569
Granted Patent B2
US 10,351,569 · App. 15/680,905 · Granted Jul 16, 2019

Indoline analogs and uses thereof

Inventor: Stephen E. Webber (San Diego, CA)
Assignee: Oncternal Therapeutics, Inc.
C07D487/04C07D209/34C07D209/38C07D209/40C07D401/06C07D403/06C07D405/06C07D409/06C07D413/06C07D417/06
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Quick Facts
Patent No.
US 10,351,569
App. No.
15/680,905
Granted
Jul 16, 2019
Kind
B2
Abstract

Indoline derivative compounds that act as EWS-FLI1 transcription factor inhibitors are provided. Also provided are pharmaceutical compositions of the indoline derivatives, methods of synthesizing the same, methods of treating using same, and assays for identifying the inhibitors of EWS-FLI1 oncoprotein.

Claims (17)

1. A compound having Formula (I):

or a stereoisomer, a pharmaceutically acceptable salt, or solvate thereof, wherein A is selected from the group consisting of —OH, D, H, F, and —NH 2 ; wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of H, Cl, —CN, —CF 3 , C 1-6 alkyl, C 1-6 alkoxy, —C(═O)NH 2 , —NO 2 , —NH 2 , and —OH; wherein R 7 , R 8 , R 10 and R 11 are independently selected from the group consisting of H, D, F, Cl, halogen, CN, CF 3 , C 1-6 alkyl, aryl, heteroaryl, —O(aryl), —O(heteroaryl), —CO 2 H, —CO 2 (C 1-6 alkyl), —NHSO 2 (C 1-6 alkyl), —NHSO 2 (aryl), —NHCONH(C 1-6 alkyl), —NHCON(C 1-6 alkyl) 2 , —N(C 1-6 alkyl)CONH 2 , —N(C 1-6 alkyl)CONH(C 1-6 alkyl), —N(C 1-6 alkyl)CON(C 1-6 alkyl) 2 , —SO 2 (C 1-6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1-6 alkyl), —SO 2 N(C 1-6 alkyl) 2 , C 3-8 cycloalkyl, and C 3-8 heterocycloalkyl; and wherein R 9 is —OCH 3 .

2. The compound of claim 1 , wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of H and Cl.

3. The compound of claim 1 , wherein A is —OH.

4. The compound of claim 1 , wherein R 7 , R 8 , R 10 , and R 11 are H.

5. The compound of claim 1 , having a Formula (I-12):

6. A compound having Formula (I):

or a stereoisomer, a pharmaceutically acceptable salt, or solvate thereof, wherein A is selected from the group consisting of —OH, D, H, F, and —NH 2 ; wherein R 7 , R 8 , R 9 , R 10 and R 11 are independently selected from the group consisting of H, D, F, Cl, halogen, CN, CF 3 , C 1-6 alkyl, aryl, heteroaryl, —O(aryl), —O(heteroaryl), —CO 2 H, —CO 2 (C 1-6 alkyl), —NHSO 2 (C 1-6 alkyl), —NHSO 2 (aryl), —NHCONH(C 1-6 alkyl), —NHCON(C 1-6 alkyl) 2 , —N(C 1-6 alkyl)CONH 2 , —N(C 1-6 alkyl)CONH(C 1-6 alkyl), —N(C 1-6 alkyl)CON(C 1-6 alkyl) 2 , —SO 2 (C 1-6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1-6 alkyl), —SO 2 N(C 1-6 alkyl) 2 , C 3-8 cycloalkyl, and C 3-8 heterocycloalkyl; and wherein R 1 and R 4 are Cl and R 2 and R 3 are H.

7. The compound of claim 6 , wherein A is —OH.

8. The compound of claim 6 , wherein R 7 , R 8 , R 10 , and R 11 are H.

9. A compound having Formula (II):

or a stereoisomer, a pharmaceutically acceptable salt, or solvate thereof, wherein A is selected from the group consisting of —OH, D, H, F, and —NH 2 ; wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of H, Cl, —CN, —CF 3 , C 1-6 alkyl, C 1-6 alkoxy, —C(═O)NH 2 , —NO 2 , —NH 2 , and —OH; R 7 , R 8 , R 10 , and R 11 are independently selected from the group consisting of H, D, F, Cl, halogen, CN, CF 3 , C 1-6 alkyl, aryl, heteroaryl, —O(aryl), —O (heteroaryl), —CO 2 H, —CO 2 (C 1-6 alkyl), —NHSO 2 (C 1-6 alkyl), —NHSO 2 (aryl), —NHCONH(C 1-6 alkyl), —NHCON(C 1-6 alkyl) 2 , —N(C 1-6 alkyl)CONH 2 , —N(C 1-6 alkyl)CONH(C 1-6 alkyl), —N(C 1-6 alkyl)CON(C 1-6 alkyl) 2 , —SO 2 (C 1-6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1-6 alkyl), —SO 2 N(C 1-6 alkyl) 2 , C 3-8 cycloalkyl, and C 3-8 heterocycloalkyl; and wherein R 12 is substituted or unsubstituted C 1-6 alkyl.

10. The compound of claim 9 , wherein R 12 is —CH 3 .

11. The compound of claim 9 , having a Formula (II-13):

12. A compound having Formula (VI):

or a stereoisomer, a pharmaceutically acceptable salt, or solvate thereof, wherein A is selected from the group consisting of —OH, D, H, F, and —NH 2 ; wherein R 1 , R 2 , R 3 , and R 4 are independently selected from the group consisting of H, Cl, —CN, —CF 3 , C 1-6 alkyl, C 1-6 alkoxy, —C(═O)NH 2 , —NO 2 , —NH 2 , and —OH; and wherein R 7 , R 8 , R 10 , and R 11 are independently selected from the group consisting of H, D, F, Cl, halogen, CN, CF 3 , C 1-6 alkyl, aryl, heteroaryl, —O(aryl), —O(heteroaryl), —CO 2 H, —CO 2 (C 1-6 alkyl), —NHSO 2 (C 1-6 alkyl), —NHSO 2 (aryl), —NHCONH(C 1-6 alkyl), —NHCON(C 1-6 alkyl) 2 , —N(C 1-6 alkyl)CONH 2 , —N(C 1-6 alkyl)CONH(C 1-6 alkyl), —N(C 1-6 alkyl)CON(C 1-6 alkyl) 2 , —SO 2 (C 1-6 alkyl), —SO 2 NH 2 , —SO 2 NH(C 1-6 alkyl), —SO 2 N(C 1-6 alkyl) 2 , C 3-8 cycloalkyl, and C 3-8 heterocycloalkyl.

13. The compound of claim 12 , wherein the compound has a Formula (VI-20):

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 7, 2025
From: HO’OLA THERAPEUTICS INC.
To: GEORGETOWN UNIVERSITY
Reel/Frame 071621/0044 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 1, 2025
From: ONCTERNAL THERAPEUTICS, INC.
To: HO’OLA THERAPEUTICS INC.
Reel/Frame 071585/0583 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2017
From: WEBBER, STEPHEN E.
To: ONCTERNAL THERAPEUTICS, INC.
Reel/Frame 043338/0084 →
Continuity (4)
Division 15461327 · Mar 16, 2017
Provisional Application 62316156 · Mar 31, 2016
Provisional Application 62417621 · Nov 4, 2016
Related Publication 20170349600A1 · Dec 7, 2017