IP Library Granted Patent US 8,609,850
Granted Patent B2
US 8,609,850 · App. 13/620,029 · Granted Dec 17, 2013

Targeted nitroxide agents

Inventors: Peter Wipf (Pittsburgh, PA); Marie Celine Frantz (Pittsburgh, PA)
Assignee: University of Pittsburgh—Of the Commonwealth System of Higher Education
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Quick Facts
Patent No.
US 8,609,850
App. No.
13/620,029
Granted
Dec 17, 2013
Kind
B2
Abstract

Provided herein are compositions and related methods useful for free radical scavenging, with particular selectivity for mitochondria. The compounds comprise a nitroxide-containing group attached to a mitochondria-targeting group. The compounds can be cross-linked into dimers without loss of activity. Also provided herein are methods, for preventing, mitigating and treating damage caused by radiation. The method comprises delivering a compound, as described herein, to a patient in an amount and dosage regimen effective to prevent, mitigate or treat damage caused by radiation.

Claims (12)

1. A compound having the structure:

wherein X is one of

R 1 and R 2 are hydrogen, C 1 -C 6 straight or branched-chain alkyl, or a C 1 -C 6 straight or branched-chain alkyl further comprising a phenyl (C 6 H 5 ) group, that is unsubstituted or is methyl-, hydroxyl- or fluoro-substituted; R 4 is hydrogen, C 1 -C 6 straight or branched-chain alkyl, or a C 1 -C 6 straight or branched-chain alkyl further comprising a phenyl (C 6 H 5 ) group, that is unsubstituted or is methyl-, hydroxyl- or fluoro-substituted; R 3 is —NH—R 5 , —O—R 5 or —CH 2 —R 5 , and R 5 is an —N—O., —N—OH or N═O containing group; R is —C(O)—R 6 , —C(O)O—R 6 , or —P(O)—(R 6 ) 2 , wherein R 6 is C 1 -C 6 straight or branched-chain alkyl or C 1 -C 6 straight or branched-chain alkyl further comprising one or more phenyl (—C 6 H 5 ) groups that are independently unsubstituted, or methyl-, ethyl-, hydroxyl- or fluoro-substituted; and wherein the compound is not XJB-5-208.

2. The compound of claim 1 , having the structure

or the structure

3. The compound of claim 2 , having the structure

4. The compound of claim 1 , in which R is Ac, Boc, Cbz, or —P(O)-Ph 2 .

5. The compound of claim 1 , in which R 1 , R 2 , R 4 and R 6 are independently chosen from hydrogen, methyl, ethyl, propyl, 2-propyl, butyl, t-butyl, pentyl, hexyl, benzyl, hydroxybenzyl, phenyl and hydroxyphenyl.

6. The compound of claim 1 , wherein when X is —CH═CR 4 —, R 4 is hydrogen, methyl or ethyl.

7. The compound of claim 1 , wherein X is

8. The compound of claim 1 wherein X is

9. A pharmaceutical composition comprising a therapeutically effective amount of a compound of claim 1 , and a pharmaceutically acceptable carrier.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 12, 2013
From: WIPF, PETER; FRANTZ, MARIE CELINE
To: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Reel/Frame 031584/0638 →
CONFIRMATORY LICENSE Recorded Oct 26, 2012
From: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029199/0135 →
Continuity (5)
Continuation 12505294 · Jul 17, 2009
Provisional Application 61081585 · Jul 17, 2008
Provisional Application 61158569 · Mar 9, 2009
Provisional Application 61178570 · May 15, 2009
Related Publication 20130102626A1 · Apr 25, 2013