| Literature DB >> 8875939 |
H R Onishi1, B A Pelak, L S Gerckens, L L Silver, F M Kahan, M H Chen, A A Patchett, S M Galloway, S A Hyland, M S Anderson, C R Raetz.
Abstract
Lipid A constitutes the outer monolayer of the outer membrane of Gram-negative bacteria and is essential for bacterial growth. Synthetic antibacterials were identified that inhibit the second enzyme (a unique deacetylase) of lipid A biosynthesis. The inhibitors are chiral hydroxamic acids bearing certain hydrophobic aromatic moieties. They may bind to a metal in the active site of the deacetylase. The most potent analog (with an inhibition constant of about 50 nM) displayed a minimal inhibitory concentration of about 1 microgram per milliliter against Escherichia coli, caused three logs of bacterial killing in 4 hours, and cured mice infected with a lethal intraperitoneal dose of E. coli.Entities:
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Year: 1996 PMID: 8875939 DOI: 10.1126/science.274.5289.980
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728