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Bioorg Med Chem Lett. 2008 Nov 15;18(22):5963-6. doi: 10.1016/j.bmcl.2008.07.130. Epub 2008 Aug 12.

Mechanism-based inhibitors of MenE, an acyl-CoA synthetase involved in bacterial menaquinone biosynthesis.

Author information

1
Molecular Pharmacology & Chemistry Program and Tri-Institutional Research Program, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, Box 422, New York, NY 10065, USA.

Abstract

Menaquinone (vitamin K(2)) is an essential component of the electron transfer chain in many pathogens, including Mycobacterium tuberculosis and Staphylococcus aureus, and menaquinone biosynthesis is a potential target for antibiotic drug discovery. We report herein a series of mechanism-based inhibitors of MenE, an acyl-CoA synthetase that catalyzes adenylation and thioesterification of o-succinylbenzoic acid (OSB) during menaquinone biosynthesis. The most potent compound inhibits MenE with an IC(50) value of 5.7microM.

PMID:
18762421
PMCID:
PMC2628629
DOI:
10.1016/j.bmcl.2008.07.130
[Indexed for MEDLINE]
Free PMC Article

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