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细菌 N-琥珀酰-L,L-二氨基庚二酸去琥珀酰酶(DapE)抑制剂及其体外抗菌活性的研究。

Inhibitors of bacterial N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) and demonstration of in vitro antimicrobial activity.

机构信息

Department of Chemistry, Loyola University, 6525 North Sheridan Road, Chicago, IL 60626, USA.

出版信息

Bioorg Med Chem Lett. 2009 Nov 15;19(22):6350-2. doi: 10.1016/j.bmcl.2009.09.077. Epub 2009 Sep 24.

Abstract

The dapE-encoded N-succinyl-L,L-diaminopimelic acid desuccinylase (DapE) is a critical bacterial enzyme for the construction of the bacterial cell wall. A screen biased toward compounds containing zinc-binding groups (ZBG's) including thiols, carboxylic acids, boronic acids, phosphonates and hydroxamates has delivered a number of micromolar inhibitors of DapE from Haemophilus influenzae, including the low micromolar inhibitor L-captopril (IC(50)=3.3 microM, K(i)=1.8 microM). In vitro antimicrobial activity was demonstrated for L-captopril against Escherichia coli.

摘要

DapE 编码的 N-琥珀酰-L,L-二氨基庚二酸去琥珀酰酶(DapE)是细菌细胞壁构建的关键酶。一个偏向于含有锌结合基团(ZBG)的化合物的筛选,包括硫醇、羧酸、硼酸、膦酸和羟肟酸,从流感嗜血杆菌中获得了一些 DapE 的微摩尔抑制剂,包括低微摩尔抑制剂 L-卡托普利(IC(50)=3.3μM,K(i)=1.8μM)。体外抗菌活性研究表明,L-卡托普利对大肠杆菌有活性。

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