Inhibition of the Bacterial Enoyl Reductase FabI by Triclosan: A Structure−Reactivity Analysis of FabI Inhibition by Triclosan Analogues
Author:
Affiliation:
1. Department of Chemistry, SUNY at Stony Brook, Stony Brook, New York 11794-3400, and Department of Pharmacological Sciences, SUNY at Stony Brook, Stony Brook, New York 11794-8651
Publisher
American Chemical Society (ACS)
Subject
Drug Discovery,Molecular Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/jm030182i
Reference37 articles.
1. Lipid biosynthesis as a target for antibacterial agents
2. Bacterial Fatty Acid Biosynthesis: Targets for Antibacterial Drug Discovery
3. Inhibitors of bacterial enoyl acyl carrier protein reductase (FabI): 2,9-disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agents
4. 1,4-Disubstituted imidazoles are potential antibacterial agents functioning as inhibitors of enoyl acyl carrier protein reductase (FabI)
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