| Literature DB >> 18554905 |
Edite Verissimo1, Neil Berry, Peter Gibbons, M Lurdes S Cristiano, Philip J Rosenthal, Jiri Gut, Stephen A Ward, Paul M O'Neill.
Abstract
The structure-based design, chemical synthesis and in vitro activity evaluation of various falcipain inhibitors derived from 2-pyridone are reported. These compounds contain a peptidomimetic binding determinant and a Michael acceptor terminal moiety capable of deactivating the cysteine protease active site.Entities:
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Year: 2008 PMID: 18554905 DOI: 10.1016/j.bmcl.2008.05.068
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823