IP Library › Granted Patent US 7,335,681
Granted Patent B2
US 7,335,681 · App. 11/522,063 · Granted Feb 26, 2008

Amino ceramide-like compounds and therapeutic methods of use

Assignee: The Regents of the University of Michigan
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Quick Facts
Patent No.
US 7,335,681
App. No.
11/522,063
Granted
Feb 26, 2008
Kind
B2
Abstract

Novel prodrugs of amino ceramide-like compounds are provided which inhibit glucosyl ceramide (GlcCer) formation by inhibiting the enzyme GlcCer synthase, thereby lowering the level of glycosphingolipids. The compounds of the present invention have improved GlcCer synthase inhibition activity and are therefore highly useful in therapeutic methods for treating various conditions and diseases associated with altered glycosphingolipid levels.

Claims (36)

1. A compound represented by the formula:

or a pharmaceutically acceptable salt thereof,

wherein

R 1 is an aromatic structure, an alicyclic structure, a branched aliphatic structure or a linear aliphatic group having 5 to 15 carbons;

R 2 is an aliphatic chain having 10 to 18 carbons;

R 3 is an acyclic tertiary amine; and

R 4 is an in vivo hydrolyzable group.

2. The compound of claim 1 wherein R 1 is 4-hydroxyphenyl.

3. The compound of claim 1 wherein R 1 is 3,4-ethylenedioxyphenyl.

4. The compound of claim 1 wherein hydrolyzable groups represented R 4 is selected from the group consisting of an acetyl, —CO(CH 2 )CH 3 and

wherein R 5 is an alkyl group.

5. A method for treating a patient having Gaucher's disease, Tay Sachs disease, Fabry's disease. Sandhoff disease or GM1 gangliosidosis, comprising the step of administering to the patient a therapeutically effective amount of the compound of claim 1 or pharmaceutically acceptable salts thereof.

6. A compound selected from the group consisting of the formula:

or a pharmaceutically acceptable salt thereof,

wherein

R 1 is an aromatic structure, an alicyclic structure, a branched aliphatic structure or a linear aliphatic group having 5 to 15 carbons;

R 2 is an aliphatic chain having 10 to 18 carbons;

R 3 is an acyclic tertiary amine;

R 4 is an in vivo hydrolyzable group or a hydrogen; and

R 6 is an in vivo hydrolyzable group.

7. The compound of claim 6 wherein R 1 is 4-hydroxyphenyl.

8. The compound of claim 6 wherein R 1 is 3,4-ethylenedioxyphenyl.

9. The compound of claim 6 wherein hydrolyzable groups represented R 4 and R 6 are independently selected from the group consisting of an acetyl, —CO(CH 2 )CH 3 and

wherein R 5 is an alkyl group.

10. A method for treating a patient having Gaucher's disease, Tay Sachs disease, Fabry's disease. Sandhoff disease or GM1 gangliosidosis, comprising the step of administering to the patient a therapeutically effective amount of the compound of claim 6 or pharmaceutically acceptable salts thereof.

11. A compound selected from the group consisting of the formulas:

or pharmaceutically acceptable salts thereof,

wherein

n is an integer from about 1 to about 19;

R 2 is an aliphatic chain having 10 to 18 carbon atoms; and

R 3 is an acyclic tertiary amine.

12. A method for treating a patient having Gaucher's disease, Tay Sachs disease, Fabry's disease. Sandhoff disease or GM1 gangliosidosis, comprising the step of administering to the patient a therapeutically effective amount of a compound selected from the group consisting of the formulas:

or pharmaceutically acceptable salts thereof, wherein

n is an integer from about 1 to about 19;

R 2 is an aliphatic chain having 10 to 18 carbon atoms; and

R 3 is an acyclic tertiary amine.

Assignments (1)
CONFIRMATORY LICENSE Recorded Nov 17, 2009
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 023526/0654 →
Continuity (4)
Division 1004486900 · Jan 10, 2002
Provisional Application 6026219600 · Jan 17, 2001
Provisional Application 6026094800 · Jan 10, 2001
Related Publication 20070072916A1 · Mar 29, 2007