| Literature DB >> 10652226 |
G Abbenante1, D M Kovacs, D L Leung, D J Craik, R E Tanzi, D P Fairlie.
Abstract
A series of inhibitors of beta-amyloid formation have been developed based on the beta-secretase cleavage site (VNL-DA) of the Swedish mutant Amyloid Precursor Protein. A simple tripeptide aldehyde was found to be the most potent (IC(50) = 700 nM) in the series displaying an inhibitory profile which is different from reported inhibitors of beta-amyloid formation. Copyright 2000 Academic Press.Entities:
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Year: 2000 PMID: 10652226 DOI: 10.1006/bbrc.2000.2098
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575