IP Library Granted Patent US 8,513,290
Granted Patent B2
US 8,513,290 · App. 13/490,693 · Granted Aug 20, 2013

Method for preparing largazole analogs and uses thereof

Inventors: Robert M. Williams (Fort Collins, CO); James E. Bradner (Cambridge, MA); Albert Bowers (Boston, MA); Tenaya Newkirk (Fort Collins, CO); Olaf G. Wiest (Notre Dame, IN)
Assignees: Colorado State University Research Foundation; Dana-Farber Cancer Institute, Inc.; University of Notre Dame du Lac
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Quick Facts
Patent No.
US 8,513,290
App. No.
13/490,693
Granted
Aug 20, 2013
Kind
B2
Abstract

Analogs of largazole are described herein. Methods of treating cancer and blood disorders using largazole and largazole analogs and pharmaceutical compositions comprising the same are additionally described herein. Methods for preparing largazole analogs are likewise described.

Claims (43)

1. A compound of Formula (I)

wherein X is S or O;

Y is NR or O, wherein R is H, lower alkyl, or lower arylalkyl;

Z is S or O; wherein at least one of X and Z is O;

R 1 is H, lower alkyl, or lower arylalkyl;

R 2 is lower alkyl, isopropyl, n-propyl, cyclopropyl, isobutyl, n-butyl, sec-butyl, or tert-butyl;

R 4 is H, (CH 2 ) n COOH, (CH 2 ) n CONHR, (CH 2 ) n CONHOH, (CH 2 ) n SR 3 , SR 5 (wherein R 5 is lower alkyl or lower aryl),

wherein n is at least 1, and wherein R 3 is H, octanoyl, acyl, SR, a higher acyl derivative, or

or a pharmaceutically acceptable salt, prodrug, or stereoisomer thereof.

2. The compound of claim 1 ,

wherein X is S or O;

Y is NH or O;

Z is S or O; wherein at least one of X and Z is O;

R 1 is H or methyl;

R 2 is lower alkyl or isopropyl;

R 4 is H, (CH 2 ) n COOH, (CH 2 ) n CONHR, (CH 2 ) n CONHOH, (CH 2 ) n SR 3 ,

wherein n is at least 1, and wherein R 3 is H, octanoyl, acyl, SR, a higher acyl derivative, or

or a pharmaceutically acceptable salt, prodrug, or stereoisomer thereof.

3. The compound of claim 1 , having the Formula (VII)

or a pharmaceutically acceptable salt, prodrug, or stereoisomer thereof.

4. The compound of claim 1 , having the Formula (IX)

or a pharmaceutically acceptable salt, prodrug, or stereoisomer thereof.

5. A pharmaceutical composition comprising a therapeutically effective amount of the compound of claim 1 and at least one pharmaceutically acceptable excipient for treating cancer in a subject.

6. A pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula (I)

wherein X is S or O;

Y is NR or O, wherein R is H, lower alkyl, or lower arylalkyl;

Z is S or O; wherein at least one of X and Z is O;

R 1 is H, lower alkyl, or lower arylalkyl;

R 2 is lower alkyl, isopropyl, n-propyl, cyclopropyl, isobutyl, n-butyl, sec-butyl, or tert-butyl;

R 4 is H, (CH 2 ) n COOH, (CH 2 ) n CONHR, (CH 2 ) n CONHOH, (CH 2 ) n SR 3 , SR 5 (wherein R 5 is lower alkyl or lower aryl),

wherein n is at least 1, and wherein R 3 is H, octanoyl, acyl, SR, a higher acyl derivative, or

or a pharmaceutically acceptable salt, prodrug, or stereoisomer thereof; and at least one pharmaceutically acceptable excipient for treating a blood disorder in a subject.

7. A pharmaceutical composition comprising a therapeutically effective amount of the compound of claim 1 and at least one pharmaceutically acceptable excipient for treating a blood disorder in a subject, wherein the blood disorder is at least one of a hemoglobinopathy or a thalassemia.

8. The pharmaceutical composition of claim 5 or 6 , wherein the subject is human.

9. A composition comprising a radiolabelled compound of Formula (I)

wherein X is S or O;

Y is NR or O, wherein R is H, lower alkyl, or lower arylalkyl;

Z is S or O; wherein at least one of X and Z is O;

R 1 is H, lower alkyl, or lower arylalkyl;

R 2 is lower alkyl, isopropyl, n-propyl, cyclopropyl, isobutyl, n-butyl, sec-butyl, or tert-butyl;

R 4 is H, (CH 2 ) n COOH, (CH 2 ) n CONHR, (CH 2 ) n CONHOH, (CH 2 ) n SR 3 , SR 5 (wherein R 5 is lower alkyl or lower aryl),

wherein n is at least 1, and wherein R 3 is H, octanoyl, acyl, SR, a higher acyl derivative, or

or a pharmaceutically acceptable salt, prodrug, or stereoisomer thereof.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 18, 2013
From: WIEST, OLAF G.
To: UNIVERSITY OF NOTRE DAME DU LAC
Reel/Frame 030637/0631 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2012
From: WILLIAMS, ROBERT M.; BOWERS, ALBERT; NEWKIRK, TENAYA; YOUNGMAN, ANN E.
To: COLORADO STATE UNIVERSITY RESEARCH FOUNDATION
Reel/Frame 028351/0080 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2012
From: BRADNER, JAMES E.
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 028351/0117 →
Continuity (4)
Division 12504508 · Jul 16, 2009
Provisional Application 61151087 · Feb 9, 2009
Provisional Application 61081653 · Jul 17, 2008
Related Publication 20120264794A1 · Oct 18, 2012