IP Library Granted Patent US 10,548,897
Granted Patent B2
US 10,548,897 · App. 15/566,565 · Granted Feb 4, 2020

KSR antagonists

Inventors: Arvin Dar (New York, NY); Neil Dhawan (New York, NY); Alex P. Scopton (New York, NY)
Assignee: Icahn School of Medicine at Mount Sinai
A61K31/517A61K31/519A61P35/00
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Quick Facts
Patent No.
US 10,548,897
App. No.
15/566,565
Granted
Feb 4, 2020
Kind
B2
Abstract

This invention relates to antagonists of Kinase Suppressor of Ras (KSR). Pharmaceutical compositions comprising KSR inhibitors and methods of treating cancer are also provided.

Claims (18)

1. A compound of Formula I:

or a pharmaceutically acceptable salt thereof, wherein:

A is selected from the group consisting of NH, N(CH 3 ), S, O, and CH 2 ;

L is selected from the group consisting of O, NH, S, and CH 2 ;

W is independently selected from the group consisting of halo and C 1-4 alkyl;

Cy 1 is selected from the group consisting of:

R 1 and R 5 are each independently selected from the group consisting of H, halo, OH, C 1-4 alkyl, and C 1-4 haloalkyl;

R 3 is selected from the group consisting of H and halo; and

R 2 and R 4 are each independently selected from the group consisting of H and halo.

2. The compound of claim 1 , wherein the compound is a compound of Formula Ib:

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 , wherein the compound is selected from the group consisting of:

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt thereof.

5. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable carrier.

6. A method of treating a disease associated with KSR in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein the patient has colon cancer.

7. The method of claim 6 , further comprising administering a therapeutically effective amount of an MEK inhibitor to the patient, wherein the MEK inhibitor is selected from the group consisting of trametinib, selumetinib, binimetinib, refametinib, pimasertib, cobimetinib, AZD8330, RO4987655, RO5126766, WX-554, E6201, PD-325901, CI-1040, GDC-0623, G-573, TAK-733, PD318088, PD98059, PD334581, 6-methoxy-7-(3-morpholin-4-yl-propoxy)-4-(4-phenoxy-phenylamino)quinoline-3-carbonitrile, and 4-[3-Chloro-4-(1-methyl-1H-imidazol-2-ylsulfanyl)phenylamino]-6-methoxy-7-(3-morpholin-4-yl-propoxy)-quinoline-3-carbonitrile.

Assignments (1)
CONFIRMATORY LICENSE Recorded Oct 18, 2017
From: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 044334/0030 →
Continuity (2)
Provisional Application 62148591 · Apr 16, 2015
Related Publication 20180256577A1 · Sep 13, 2018
Cited By (1)
US 12,351,566