| Literature DB >> 12161164 |
Gillian M Nicholas1, Lisa L Eckman, Satyajit Ray, Robert O Hughes, Jeffrey A Pfefferkorn, Sofia Barluenga, K C Nicolaou, Carole A Bewley.
Abstract
A series of bromotyrosine-derived compounds, including marine natural products and members of a psammaplin A-inspired combinatorial synthetic library, were screened for their ability to inhibit the Mycobacterium tuberculosis detoxification enzyme mycothiol-S-conjugate amidase (MCA). Correlations between the structures and their respective IC(50) values (which range from 3 microM to 2.7 mM) should prove valuable when optimizing more potent inhibitors of MCA.Entities:
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Year: 2002 PMID: 12161164 DOI: 10.1016/s0960-894x(02)00385-2
Source DB: PubMed Journal: Bioorg Med Chem Lett ISSN: 0960-894X Impact factor: 2.823