IP Library › Granted Patent US 10,588,894
Granted Patent B2
US 10,588,894 · App. 16/013,872 · Granted Mar 17, 2020

Compounds that interact with the Ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease

Inventors: Yaron R. Hadari (Harrison, NY); Luca Carta (Hartsdale, NY); Michael Schmertzler (New Canaan, CT); Theresa M. Williams (Harleysville, PA); Charles H. Reynolds (Austin, TX); Rebecca Hutcheson (Lake Peekskill, NY)
Assignee: SHY Therapeutics LLC
A61K31/4365A61K31/505A61P25/28A61P29/00A61P35/00C07D495/04C12N15/1037C12N15/1065
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,588,894
App. No.
16/013,872
Granted
Mar 17, 2020
Kind
B2
Abstract

Provided herein are methods and compositions for treating cancers, inflammatory diseases, rasopathies, and fibrotic disease involving aberrant Ras superfamily signaling through the binding of compounds to the GTP binding domain of Ras superfamily proteins including, in certain cases, K-Ras and mutants thereof, and a novel method for assaying such compositions.

Claims (16)

1. A compound of Formula VIb:

or pharmaceutically acceptable derivatives thereof,

wherein R 1b is alkyl, aryl, heteroaryl, S(O) p R 4 , or NR 5 C(O)R 4 ;

R 8b is hydrogen, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, heteroaryl, halo, pseudohalo, OR 3 , C(O)R 4 , S(O) p R 4 , NR 5 C(O)R 4 , or NR 6 R 7 ;

R 9b is hydrogen, alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, heteroaryl, halo, pseudohalo, OR 3 , C(O)R 4 , S(O) p R 4 , NR 5 C(O)R 4 , or NR 6 R 7 ; or R 8b and R 9b are combined to form a cyclic structure including the carbon atoms to which they are attached in the five-membered ring;

R 3 is hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl or arylcarbonyl;

R 4 is hydrogen, hydroxy, alkyl, haloalkyl, alkenyl, alkynyl, aryl, alkylaryl, heterocyclyl, cycloalkyl, aralkyl, alkoxy, alkenyloxy, alkynyloxy, aryloxy, alkylaryloxy, heterocyclyloxy, cycloalkyloxy, aralkoxy, or —NR 6 R 7 ;

R 5 is hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, or arylcarbonyl;

R 5b is hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, or arylcarbonyl;

R 6 and R 7 are independently selected from hydrogen, alkyl, alkenyl, alkynyl, aryl, heteroaryl, heterocyclyl, cycloalkyl, alkylcarbonyl, cycloalkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, arylsulfonyl, heteroarylsulfonyl, cycloalkylsulfonyl or alkylsulfonyl, or R 6 and R 7 are combined to form a cyclic structure including the nitrogen atom to which they are both attached; and

p is 0-2.

2. The compound of claim 1 , wherein the compound of Formula VIb is selected from the group consisting of:

3. A method of inhibiting the function of one or more members of the Ras superfamily, comprising administering to a subject the compound of claim 1 .

4. A method of inhibiting the function of one or more members of the Ras superfamily, comprising administering to a subject the compound of claim 2 .

5. A pharmaceutical composition comprising the compound of claim 1 .

6. A pharmaceutical composition comprising the compound of claim 2 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 21, 2019
From: CARTA, LUCA; WILLIAMS, THERESA M.; HUTCHESON, REBECCA; SCHMERTZLER, MICHAEL; HADARI, YARON R.; REYNOLDS, CHARLES H.
To: SHY THERAPEUTICS LLC
Reel/Frame 048397/0470 →
Continuity (2)
Provisional Application 62523114 · Jun 21, 2017
Related Publication 20190022074A1 · Jan 24, 2019
Cited By (2)
US 12,391,705 US 12,653,810