Synthesis and Evaluation of Calpain Inhibitors Carrying Muscle Cell Targeting Groups

Author(s): P. Weyermann , H. Herzner , C. Lescop , H. Siendt , R. Bolliger , M. Hennebohle , C. Rummey , A. Briguet , I. Courdier-Fruh , M. Erb , M. Foster , J.P. Magyar , A. von Sprecher , T. Meier .

Journal Name: Letters in Drug Design & Discovery

Volume 3 , Issue 3 , 2006

Become EABM
Become Reviewer

Abstract:

Inhibition of the cysteine protease calpain is a promising strategy for the treatment of muscular dystrophies including Duchenne Muscular Dystrophy. For the treatment to be effective, uptake of the inhibitors into the muscle cells is a prerequisite. A series of α-ketoamide calpain inhibitors carrying various muscle cell targeting capping groups was synthesized. Compounds with charged or highly polar targeting groups were not able to cross the cellular membrane. Introduction of lipoic acid as end cap yielded cell permeable calpain inhibitors with nanomolar potency.

Keywords: Calpain inhibitor, ketoamide, duchenne muscular dystrophy, lipoic acid

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 3
ISSUE: 3
Year: 2006
Page: [152 - 158]
Pages: 7
DOI: 10.2174/157018006776286916
Price: $58

Article Metrics

PDF: 7