IP Library Granted Patent US 11,052,154
Granted Patent B2
US 11,052,154 · App. 16/349,689 · Granted Jul 6, 2021

Ras protein degradation inducing molecule and pharmaceutical composition

Inventors: Etsuko Miyamoto (Tokyo, JP); Masaaki Ozawa (Tokyo, JP)
Assignee: Tokyo University of Science Foundation
A61K47/545A61K38/05A61P35/00
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Quick Facts
Patent No.
US 11,052,154
App. No.
16/349,689
Granted
Jul 6, 2021
Kind
B2
Abstract

A Ras protein degradation inducing molecule that can induce degradation of Ras proteins, and a pharmaceutical composition that contains this Ras protein degradation inducing molecule are provided. The Ras protein degradation inducing molecule is a conjugate of a Ras protein affinity molecule which has affinity to Ras proteins, and a proteolysis-inducing tag which has affinity to protease and does not inhibit proteolysis of proteins by the protease.

Claims (10)

1. A Ras protein-degradation inducing molecule, wherein the Ras protein-degradation inducing molecule is a conjugate of a Ras protein affinity molecule that has an affinity with a Ras protein, and a protein-degradation inducing tag that has an affinity with a 26S proteasome and does not inhibit degradation of a protein by the 26S proteasome, with the proviso that the conjugate excludes a fusion protein; and the Ras protein-degradation inducing molecule is capable of inducing degradation of the Ras protein.

2. The Ras protein-degradation inducing molecule according to claim 1 , wherein the Ras protein-degradation inducing molecule is capable of inducing degradation of the Ras protein in a ubiquitin-independent manner.

3. The Ras protein-degradation inducing molecule according to claim 1 , wherein the protein-degradation inducing tag has a structure represented by the following formula (I), or has a structure where a 26S proteasome inhibitory activity of a 26S proteasome inhibitor is inactivated, or has a structure of a proteasome activator:

wherein in the formula (I), R 1 and R 2 each independently represent a hydrocarbon group having 1 to 20 carbon atoms, an alkoxy group having 1 to 20 carbon atoms, an aryloxy group having 6 to 20 carbon atoms, a hydroxy group, a carboxy group, an amino group, or a halogen group.

4. The Ras protein-degradation inducing molecule according to claim 3 , wherein the proteasome inhibitory activity is an inhibitory activity against at least one selected from the group consisting of a caspase-like activity, a trypsin-like activity, and a chymotrypsin-like activity.

5. A pharmaceutical composition comprising the Ras protein-degradation inducing molecule according to claim 1 .

6. The pharmaceutical composition according to claim 5 , wherein the pharmaceutical composition is used for preventing or treating a Ras protein-mediated disease or condition.

7. The pharmaceutical composition according to claim 6 , wherein the Ras protein-mediated disease or condition is a cancer, an immune disease, an infection, a neurological disease, a RAS/MAPK syndrome, cirrhosis, chronic hepatitis, or a memory impairment.

8. The pharmaceutical composition according to claim 7 , wherein the Ras protein-mediated disease or condition is a cancer.

9. The Ras protein-degradation inducing molecule according to claim 1 , wherein the Ras protein-degradation inducing molecule is represented by the following formula:

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2019
From: MIYAMOTO, ETSUKO; OZAWA, MASAAKI
To: TOKYO UNIVERSITY OF SCIENCE FOUNDATION
Reel/Frame 049428/0391 →
Priority Claims (1)
JP JP2016-222683 · Nov 15, 2016 · national
Continuity (1)
Related Publication 20200000927A1 · Jan 2, 2020
Cited By (2)
US 12,448,399 US 12,552,783