IP Library Granted Patent US 10,689,356
Granted Patent B2
US 10,689,356 · App. 15/764,088 · Granted Jun 23, 2020

Inhibitors of KRAS G12C mutant proteins

Inventors: Liansheng Li (San Diego, CA); Jun Feng (San Diego, CA); Yun Oliver Long (San Diego, CA); Yuan Liu (San Diego, CA); Pingda Ren (San Diego, CA); Yi Liu (San Diego, CA)
Assignee: ARAXES PHARMA LLC
C07D401/04A61K9/0019A61K9/0053A61K31/4375A61K31/4725A61P35/00C07D471/04
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Quick Facts
Patent No.
US 10,689,356
App. No.
15/764,088
Granted
Jun 23, 2020
Kind
B2
Abstract

Compounds having activity as inhibitors of G12C mutant KRAS protein are provided. The compounds have the following structure (I): or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, wherein A, R 1 , R 3a , R 3b , R 4a , R 4b , G 2 , G 3 , G 4 , m 1 , m 2 , m 3 , m 4 , L 1 , L 2 and E are as defined herein. Methods associated with preparation and use of such compounds, pharmaceutical compositions comprising such compounds and methods to modulate the activity of G12C mutant KRAS protein for treatment of disorders, such as cancer, are also provided.

Claims (35)

1. A compound having one of the following structures (Ia′), (Ib′) or (Ic′):

or a pharmaceutically acceptable salt, tautomer, stereoisomer or prodrug thereof, wherein:

G 2 ′ G 3 and G 4 are each independently N or CR, where R is H, cyano, halo or C 1 -C 6 alkyl;

R 1 is phenyl;

R 2a and R 2b are independently H or hydroxyl;

R 3a is H;

R 3b is, at each occurrence, independently H, —OH, —NH 2 , —CO 2 H, halo, cyano, C 1 -C 6 alkyl, C 2 -C 6 alkynyl, hydroxylalkly, aminylalkyl, alkylaminylalkyl, cyanoalkyl, carboxyalkyl, aminocarbonylalkyl or aminocarbonyl;

R 4a is H;

R 4b is, at each occurrence, independently H, —OH, —NH 2 , —CO 2 H, halo, cyano, C 1 -C 6 alkyl, C 2 -C 6 alkynyl, hydroxylalkly, aminylalkyl, alkylaminylalkyl, cyanoalkyl, carboxyalkyl, aminocarbonylalkyl or aminocarbonyl;

L 1 is a bond;

L 2 is a linker of one, two or three atoms in length, the linker comprising carbon or nitrogen atoms, or combinations thereof;

m 1 and m 2 , are each independently 1 or 2;

m 3 and m 4 are each independently 1, 2 or 3;

Q is —C(═O)—;

R 7 is H, —OH, —CN or C 1 -C 6 alkyl;

R 8 is H, C 1 -C 6 alkyl or hydroxylalkyl;

represents a double bond; and

R 9 and R 10 are each H,

wherein all valences are satisfied.

2. The compound of claim 1 , wherein the compound has one of the following structures (Ia″), (Ib″) or (Ic″):

3. The compound of claim 1 , wherein R 1 is substituted with one or more substituent selected from halo, hydroxyl, cyano, aminocarbonyl, formyl, C 1 -C 6 alkyl, C 1 -C 6 alkylsulfonyl, C 1 -C 6 haloalkyl, C 3 -C 8 cycloalkyl, C 1 -C 6 alkoxy, C 1 -C 6 hydroxylalkyl, C 1 -C 6 alkoxyalkyl, C 1 -C 6 aminoalkyl, aliphatic heterocyclyl, heteroaryl, heteroarylaminyl and aryl.

4. The compound of claim 1 , wherein R 1 is substituted with one or more substituent selected from chloro, hydroxyl and cyclopropyl.

5. The compound of claim 1 , wherein R 1 has one of the following structures:

6. The compound of claim 1 , wherein L 2 is —NH—, —NHCH 2 —; —NHC(═O)— or —NHC(═NOH)—.

7. The compound of claim 1 , wherein each R 3b and R 4b are H.

8. The compound of claim 1 , wherein the compound has one of the following structures:

9. A pharmaceutical composition comprising a compound of claim 1 and a pharmaceutically acceptable carrier.

10. A method for treatment of cancer, the method comprising administering an effective amount of the pharmaceutical composition of claim 9 to a subject in need thereof.

11. A method for regulating activity of a KRAS, HRAS or NRAS G12C mutant protein, the method comprising reacting the KRAS G12C mutant protein with the compound of claim 1 .

12. A method for inhibiting proliferation of a cell population, the method comprising contacting the cell population with the compound of claim 1 .

13. A method for treating a cancer mediated by a KRAS G12C, HRAS G12C or NRAS G12C mutation in a subject in need thereof, the method comprising:

determining if the subject has a KRAS, HRAS or NRAS G12C mutation; and

if the subject is determined to have the KRAS, HRAS or NRAS G12C mutation, then administering to the subject a therapeutically effective amount of the pharmaceutical composition of claim 9 .

14. A method for preparing a labeled KRAS, HRAS or NRAS G12C mutant protein, the method comprising reacting the KRAS, HRAS or NRAS G12C mutant with a compound of claim 1 , to result in the labeled KRAS, HRAS or NRAS G12C protein.

15. A method for inhibiting tumor metastasis, the method comprising administering an effective amount of the pharmaceutical composition of claim 9 to a subject in need thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2021
From: JANSSEN BIOTECH, INC.
To: ARAXES PHARMA LLC
Reel/Frame 058604/0004 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 30, 2018
From: LI, LIANSHENG; FENG, JUN; LONG, YUN OLIVER; LIU, YUAN; REN, PINGDA; LIU, YI
To: ARAXES PHARMA LLC
Reel/Frame 045938/0648 →
Continuity (2)
Provisional Application 62233816 · Sep 28, 2015
Related Publication 20190055211A1 · Feb 21, 2019
Cited By (2)
US 50,527 US 12,234,244