IP Library Granted Patent US 8,748,480
Granted Patent B2
US 8,748,480 · App. 13/630,995 · Granted Jun 10, 2014

Methods for treating opioid tolerance

Inventors: Alan V. Smrcka (Rochester, NY); Jose Font (Fairport, NY); Tabetha Bonacci (Kimball, MN)
Assignee: University of Rochester
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Quick Facts
Patent No.
US 8,748,480
App. No.
13/630,995
Granted
Jun 10, 2014
Kind
B2
Abstract

The present invention relates to methods for identifying agents which bind to specific amino acid residues of the protein interaction site of G protein β protein subunit. Compounds identified in accordance with the assay of the invention and methods for using the compound for modulating at least one activity of a G protein are also provided.

Claims (12)

1. A method for ameliorating or treating a disease or condition in a subject in need thereof, wherein the disease or condition involves at least one G protein βγ subunit activity, the method comprising administering to the subject a therapeutically effective amount of a therapeutically acceptable composition comprising a compound that binds to at least one amino acid residue of the protein interaction site of the G protein β subunit,

wherein the protein binding site comprises at least one amino acid selected from the group consisting of Lys57, Tyr59, Trp99, Val100, Met101, Leu117, Tyr145, Asp186, Met188, Asp228, Asn230, Asp246, and Trp332 of SEQ ID NO:3 or 4,

wherein the compound is a compound of Formula III or a salt thereof:

wherein:

R 1 is substituted or unsubstituted alkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted cycloalkyl, or substituted or unsubstituted cycloalkenyl; and

R 2 and R 3 are independently —H or —OH;

wherein the disease or condition is opioid tolerance; whereby the disease or condition in the subject is ameliorated or treated in the subject.

2. The method of claim 1 , wherein R 2 and R 3 are —OH.

3. The method of claim 1 , wherein the substituents in the substituted alkyl, cycloalkyl, alkenyl or cycloalkenyl groups independently comprise hydroxy, carboxy, halogen, substituted alkyl, or unsubstituted alkyl.

4. The method of claim 1 , wherein R 1 is carboxy-substituted alkyl, carboxy-substituted cycloalkyl, carboxy-substituted alkenyl, or carboxy-substituted cycloalkenyl.

5. The method of claim 1 , wherein the compound is selected from the group consisting of:

any salts thereof, and any combinations thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Apr 22, 2019
From: UNIVERSITY OF ROCHESTER
To: NATIONAL INSTITUTES OF HEALTH - DIRECTOR DEITR
Reel/Frame 048958/0674 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2014
From: SMRCKA, ALAN V; FONT, JOSE; BONACCI, TABETHA
To: UNIVERSITY OF ROCHESTER
Reel/Frame 032793/0413 →
Continuity (3)
Continuation 11885981
Provisional Application 60659267 · Mar 7, 2005
Related Publication 20130116313A1 · May 9, 2013