IP Library Granted Patent US 9,604,907
Granted Patent B2
US 9,604,907 · App. 14/165,090 · Granted Mar 28, 2017

Methods of facilitating neural cell survival using non-peptide and peptide BDNF neurotrophin mimetics

Inventors: Frank M. Longo (Menlo Park, CA); Stephen M. Massa (Burlingame, CA)
Assignees: The University of North Carolina at Chapel Hill; The Regents of The University of California; The United States of America as represented by the Department of Veterans Affairs
C07C215/68A61K31/40A61K31/401A61K31/4178A61K38/185C07K5/0823C07K5/1016
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Quick Facts
Patent No.
US 9,604,907
App. No.
14/165,090
Granted
Mar 28, 2017
Kind
B2
Abstract

Methods and compounds for treating neurological and other disorders are provided. Included is the administering to a subject in need thereof an effective amount of a compound having binding and/or modulation specificity for a TrkB receptor molecule.

Claims (29)

1. A method of treating a disorder in a subject in need thereof, comprising administering to the subject an effective amount of a compound represented by Formula (VII):

or a pharmaceutically acceptable salt thereof,

wherein:

m and n are independently 2;

each L 9 and L 10 is C 1 -C 5 alkylene;

X 20 and X 21 are N;

X 22 is halo; and

each D 15 and each D 16 are hydroxyl;

and

wherein the disorder is selected from the group consisting of Alzheimer's disease, Huntington's disease, amyotrophic lateral sclerosis, Rett syndrome, Parkinson's disease, spinal cord injury, stroke, ischemia, brain injury, motor neuron disease, multiple sclerosis, HIV dementia, peripheral nerve injury, hearing loss, and obesity.

2. The method of claim 1 , wherein the subject is a human subject.

3. The method of claim 1 , wherein the compound is represented by the structure:

or a pharmaceutically acceptable salt thereof.

4. A method of facilitating neuronal or other cell survival, comprising contacting a cell with a compound represented by Formula (VII):

or a pharmaceutically acceptable salt thereof,

wherein:

m and n are independently 2;

each L 9 and L 10 is C 1 -C 5 alkylene;

X 20 and X 21 are N;

X 22 is halo; and

each D 15 and each D 16 are hydroxyl.

5. The method of claim 4 , wherein the compound is represented by the structure:

or a pharmaceutically acceptable salt thereof.

6. The method of claim 4 , wherein the contacting is done in vitro.

7. The method of claim 1 , wherein the compound is formulated in a unit dosage form comprising said compound and a pharmaceutically acceptable carrier.

8. The method of claim 4 , wherein the compound is formulated in a unit dosage form comprising said compound and a pharmaceutically acceptable carrier.

9. The method of claim 1 or 4 , wherein each L 9 and each L 10 are C 1 -C 3 alkylene.

10. The method of claim 8 , wherein each L 9 and each L 10 are C 2 alkylene.

11. The method of claim 1 , wherein the disorder is selected from the group consisting of Alzheimer's disease, Huntington's disease, Rett syndrome, stroke, multiple sclerosis, and Parkinson's disease.

Assignments (3)
CONFIRMATORY LICENSE Recorded Sep 29, 2014
From: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 033845/0704 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2014
From: LONGO, FRANK M.
To: THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL
Reel/Frame 032913/0019 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 16, 2014
From: MASSA, STEPHEN M.
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA; THE U.S. GOVERNMENT REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS
Reel/Frame 032913/0744 →
Continuity (3)
Division 11449381 · Jun 8, 2006
Provisional Application 60688767 · Jun 8, 2005
Related Publication 20140200277A1 · Jul 17, 2014