US 6,888,015 B2Granted

Sphingolipid synthesis inhibitor

AssigneeJapan Science and Technology Agency

InventorsShu Kobayashi, Kentaro Hanada

Life of this patent

Estimating the term…

Abstract

A inhibitor of sphingolipids synthesis comprising a compound represented by general formula A. Desirably, a novel inhibitor of sphingolipids synthesis comprising (1R, 3R) N-(3-hydroxy-1-hydroxymethyl-3-phenylpropyl) alkaneamide, wherein carbon number of alkanoyl group is 8-16. (in the formula, X is an aliphatic alkyl group, desirably is an aliphatic alkyl group having 7 to 15 carbon atoms).

Claims6

Dependent claims

A compound of general formula A,

wherein, X is an aliphatic alkyl group.

Dependencies are inferred from the claim text.

Facts

Application: 10/472,379Filed 19 Apr 2002
Priority: JP 2001-1339291 May 2001
Published: US 2004/0092600 A113 May 2004
Granted: 3 May 2005
Term ends: Not estimatedThe source records don’t support an estimate.

Classification6 codes

C07C 233/18
With the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom: having the carbon atom of…
A61K 31/165
Amides, e.g. hydroxamic acids: having aromatic rings, e.g. colchicine, atenolol, progabide
A61P 43/00
Drugs for specific purposes, not provided for in groups a61p1/00-a61p41/00
C07C
Acyclic or carbocyclic compounds

Family

US 2004/0092600 A1Pre-grant publication · published 13 May 2004
US 6,888,015 B2This patent

From the US filing history. Foreign family members aren’t listed.

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