| Literature DB >> 6863235 |
N Katunuma, T Towatari, M Tamai, K Hanada.
Abstract
Efficient methods were developed for synthesizing synthetic substrates for assays of cathepsin B and cathepsin L. Several 2-naphthylamide compounds with a blocked NH2-terminus, Suc-Tyr-Met-NA, beta-Ala-Tyr-Met-NA, and D-Leu-Tyr-Met-NA, were specific and sensitive substrates for cathepsin L and cathepsin B; they were not specific for cathepsin L only, because all of them were also hydrolyzed by cathepsin B. Some kinetic constants for the hydrolyses of these three synthetic substrates by cathepsin B and cathepsin L are given.Entities:
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Year: 1983 PMID: 6863235 DOI: 10.1093/oxfordjournals.jbchem.a134238
Source DB: PubMed Journal: J Biochem ISSN: 0021-924X Impact factor: 3.387