IP Library › Granted Patent US 10,730,842
Granted Patent B2
US 10,730,842 · App. 15/756,917 · Granted Aug 4, 2020

Small molecule inhibitors of DYRK1A and uses thereof

Inventors: Christopher Hulme (Tucson, AZ); Travis Dunckley (Phoenix, AZ); Yeng-Jeng Shaw (Tucson, AZ)
Assignees: ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA; THE TRANSLATIONAL GENOMICS RESEARCH INSTITUTE
C07D235/06A61K31/4184A61K31/4439A61K31/4545A61K31/506A61K31/5377A61K45/06C07D401/04C07D401/14C07D403/04C07D405/04C07D405/14C07D409/04C07D471/04
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Quick Facts
Patent No.
US 10,730,842
App. No.
15/756,917
Granted
Aug 4, 2020
Kind
B2
Abstract

This invention is in the field of medicinal chemistry. In particular, the invention relates to a new class of small-molecules having a benzimidazole or imidazopyridine structure which function as inhibitors of DYRK1A protein, and their use as therapeutics for the treatment of Alzheimer's disease, Down syndrome, glioblastoma, autoimmune diseases, inflammatory disorders (e.g., airway inflammation), and other diseases.

Claims (20)

1. A compound having

pharmaceutically acceptable salts thereof, and/or solvates thereof;

wherein R1 is selected from hydrogen,

wherein each of R2 and R3 is independently selected from hydrogen,

wherein R4 is selected from hydrogen,

wherein R5 is selected from hydrogen, alkoxy, alkylsulfonyl, cyano, carboxy, ester, amido, substituted amido, sulfonamide, substituted sulfonamide, methylenedioxy, heterocyclyl alkyl, heterocyclyl, and heterocyclyl alkyl amido, a lipophilic moiety comprising ether functionality, methyl, ethyl, (CH 2 ) 3 ,

wherein R6 is selected from hydrogen, C1-C4 alkyl, heterocyclyl alkyl, heteroaryl alkyl, aryl alkyl, aryl, heterocyclyl, and heteroaryl;

wherein R7 is selected from hydrogen, alkoxy, alkylsulfonyl, cyano, carboxy, ester, amido, substituted amido, sulfonamide, substituted sulfonamide, methylenedioxy, heterocyclyl alkyl, heterocyclyl, and heterocyclyl alkyl amido, a lipophilic moiety comprising ether functionality, methyl, ethyl, (CH 2 ) 3 ,

and

wherein X, Y, Z are independently N, C or CO,

wherein R1, R2, R3, and R4 cannot each be hydrogen.

2. The compound of claim 1 , wherein said compound is selected from the following compounds:

3. The compound of claim 1 , wherein the compound is within a pharmaceutical composition.

4. A method of treating, ameliorating, or preventing a disorder related to DYRK1A activity in a patient comprising administering to said patient a therapeutically effective amount of the pharmaceutical composition of claim 3 .

5. The method of claim 4 , wherein said disorder related to DYRK1A activity is Alzheimer's disease, Down syndrome, Huntington's disease, Parkinson's disease, an autoimmune disease, an inflammatory disorder, or cancer.

6. The method of claim 5 , wherein said patient is a human patient.

7. The method of claim 5 , further comprising administering to said patient one or more agents for treating Alzheimer's disease, Down syndrome, Huntington's disease, Parkinson's disease, an autoimmune disease, an inflammatory disorder, or cancer.

8. A kit comprising a compound of claim 1 and instructions for administering said compound to a patient having a disorder related to DYRK1 activity.

9. The kit of claim 8 , wherein the disorder related to DYRK1 activity is Alzheimer's disease, Down syndrome, Huntington's disease, Parkinson's disease, autoimmune disease, an inflammatory disorder, or cancer.

10. The kit of claim 8 , further comprising one or more agents for treating Alzheimer's disease, Down syndrome, Huntington's disease, Parkinson's disease, autoimmune disease, an inflammatory disorder, or cancer.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2019
From: HULME, CHRISTOPHER; SHAW, YENG-JENG
To: ARIZONA BOARD OF REGENTS ON BEHALF OF THE UNIVERSITY OF ARIZONA
Reel/Frame 047985/0425 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2019
From: DUNCKLEY, TRAVIS
To: THE TRANSLATIONAL GENOMICS RESEARCH INSTITUTE
Reel/Frame 047985/0469 →
Continuity (2)
Provisional Application 62213904 · Sep 3, 2015
Related Publication 20190062284A1 · Feb 28, 2019
Cited By (1)
US 12,419,865