IP Library › Granted Patent US 11,026,930
Granted Patent B1
US 11,026,930 · App. 16/847,467 · Granted Jun 8, 2021

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 (St. Petersburg, FL); 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
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Quick Facts
Patent No.
US 11,026,930
App. No.
16/847,467
Granted
Jun 8, 2021
Kind
B1
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 (19)

1. An assay for identifying a compound as a modulator of Ras activity, wherein the assay comprises:

a) contacting a compound with a Ras protein;

b) incubating a cyanine-labeled GTP with the compound and the Ras protein; and

c) measuring the amount of the cyanine-labeled GTP bound to the Ras protein.

2. The assay of claim 1 , wherein the assay is a cell-free assay.

3. The assay of claim 1 , wherein the Ras protein is DIRAS I; DIRAS2; DIRAS3; ERAS; GEM; HRAS; KRAS; MRAS; NKIRAS1; NKIRAS2; NRAS; RALA; RALB; RAPIA; RAPIB; RAP2 Å; RAP2B; RAP2C; RASD1; RASD2; RASLIOA; RASL10B; RASLI IA; RASLI IB; RASL12; REMI; REM2; RERG; RERGL; RRAD; RRAS; or RRAS2.

4. The assay of claim 1 , wherein the Ras protein is HRAS; KRAS; or NRAS, or a mutant thereof.

5. The assay of claim 1 , wherein the Ras protein is immobilized.

6. The assay of claim 1 , wherein the compound competitively inhibits GTP binding to the Ras GTP binding domain.

7. The assay of claim 1 , wherein the compound binds to the Ras protein GTP binding domain with greater than 25% inhibition at 20 uM.

8. The assay of claim 1 , wherein the compound has a binding affinity (K d ) to the Ras protein GTP binding domain of less than 10 uM.

9. The assay of claim 1 , wherein the compound inhibits the Ras activity and has an IC50 value of less than 10 uM.

10. The assay of claim 1 , wherein the compound inhibits binding of the cyanine-labeled GTP with an IC50 value of less than 10 uM.

11. The assay of claim 1 , wherein the cyanine-labeled GTP is a Cy3- or a Cy5-labeled GTP.

12. The assay of claim 1 , wherein the assay is a GTP-binding competition assay.

13. The assay of claim 1 , wherein the Ras protein is a KRas G12D mutant, KRas G12C mutant, or KRas Q61H mutant.

14. The assay of claim 1 , wherein the Ras protein is wild-type KRas.

15. The assay of claim 1 , wherein the compound has a molecular weight of less than 2000 Daltons.

16. The assay of claim 1 , wherein the compound has a molecular weight of less than 750 Daltons.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 2, 2021
From: CARTA, LUCA; WILLIAMS, THERESA M.; HUTCHESON, REBECCA; SCHMERTZLER, MICHAEL; HADARI, YARON R.; REYNOLDS, CHARLES H.
To: SHY THERAPEUTICS, INC.
Reel/Frame 057991/0977 →
Continuity (3)
Continuation 16654934 · Oct 16, 2019
Continuation 16013872 · Jun 20, 2018
Provisional Application 62523114 · Jun 21, 2017
Cited By (2)
US 12,391,705 US 12,653,810