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抑制脂质A生物合成的抗菌剂。

Antibacterial agents that inhibit lipid A biosynthesis.

作者信息

Onishi H R, Pelak B A, Gerckens L S, Silver L L, Kahan F M, Chen M H, Patchett A A, Galloway S M, Hyland S A, Anderson M S, Raetz C R

机构信息

Department of Microbiology, Merck Research Laboratories, Rahway, NJ 07065, USA.

出版信息

Science. 1996 Nov 8;274(5289):980-2. doi: 10.1126/science.274.5289.980.

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.

摘要

脂多糖A构成革兰氏阴性菌外膜的外层单分子层,对细菌生长至关重要。已鉴定出抑制脂多糖A生物合成的第二种酶(一种独特的脱乙酰酶)的合成抗菌剂。这些抑制剂是带有某些疏水芳香基团的手性异羟肟酸。它们可能与脱乙酰酶活性位点中的金属结合。最有效的类似物(抑制常数约为50 nM)对大肠杆菌的最低抑菌浓度约为每毫升1微克,在4小时内导致细菌数量减少三个对数,并治愈了感染致死剂量腹腔注射大肠杆菌的小鼠。

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