Amino ceramide-like compounds and therapeutic methods of use
View Patent ↗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.
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.