IP Library Granted Patent US 7,465,710
Granted Patent B2
US 7,465,710 · App. 11/224,759 · Granted Dec 16, 2008

Compounds for control of appetite, blood pressure, cardiovascular response, libido, and circadian rhythm

Assignee: University of Cincinnati
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Quick Facts
Patent No.
US 7,465,710
App. No.
11/224,759
Granted
Dec 16, 2008
Kind
B2
Abstract

This invention relates generally to dipeptides and tripeptides and to methods for pharmaceutical treatment of mammals using analogs of such dipeptides and tripeptides. More specifically, the invention relates to tripeptides and their analogs, to pharmaceutical compositions containing such dipeptides and tripeptides and to methods of treatment of mammals using such dipeptides and tripeptides. In addition, the invention relates to methods of treatment of mammals using such dipeptides and tripeptides for control of appetite, blood pressure, cardiovascular response, libido, and circadian rhythm.

Claims (15)

1. A compound having the formula:

Ac-(A1-A2-A3) n -NH 2

wherein:

A1 is a D or L-amino acid chosen from Cys, Leu, Dap, Trp, Gln, a tethered amino acid with an indole ring, Phe, Hyp, any Trp derivative; CαMe-Trp, CαMe-Gln, Des-amino-Trp, Pyr, Bth, Nal, Tcc, Asn, Nva, Abu, Tyr, Tic-OH, Tip, and Dip;

A2 is a D or L-amino acid chosen from Cys, Trp, Arg, Nα-Me-Arg, CαMe-Arg, Orn, Cit, hArg(R)2, and Lys-ε-NH—R, where R is chosen from hydrogen, alkyl, aryl, aralkyl, and alkylaryl;

A3 is a D or L-amino acid chosen from Glu, N-Me-Tyr, CαMe-Tyr, Tic-OH, Tic, Dip, Trp, Phe, des-carboxylic-Tyr (tyramine), and Tyr-(R), where R is hydrogen or a lipophilic group;

n is 1, 2, or 3; and

each bond between two amino acids or amino acid derivatives, represented by a dash (“—”), can be either a peptide bond or a pseudopeptide bond or a pharmaceutically acceptable salt thereof.

2. A therapeutic composition capable of controlling an NPY mediated physiological response comprising a therapeutically effective amount of the compound of claim 1 , together with a pharmaceutically acceptable carrier substance.

3. The composition of claim 2 , wherein said composition is in the form of a pill, tablet, or capsule for oral administration to a subject in need of said compound.

4. The composition of claim 2 , wherein said composition is in the form of a liquid for oral administration to a subject in need of said compound.

5. The composition of claim 2 , wherein said composition being is in the form of a liquid for nasal administration as drops or spray to a subject in need of said composition.

6. The composition of claim 2 , wherein said composition is in the form of a liquid for intravenous, subcutaneous, parenteral, or intraperitoneal administration to a subject in need of said composition.

7. The composition of claim 2 , wherein said composition is in the form of a biodegradable sustained-release composition for intramuscular administration to a subject in need of said composition.

8. The composition of claim 2 , wherein said composition includes a lipophilic salt and is suitable for administration in the form of an oil emulsion or dispersion to a subject in need of said composition.

Assignments (1)
CONFIRMATORY LICENSE Recorded Mar 9, 2015
From: UNIVERSITY OF CINCINNATI
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 035145/0399 →
Continuity (5)
Division 1084846900 · May 18, 2004
Division 0961836100 · Jul 18, 2000
Continuation In Part 0944991400 · Dec 2, 1999
Division 0890740300 · Aug 7, 1997
Related Publication 20060009395A1 · Jan 12, 2006