环丙沙星
化学
流出
噻吩
最小抑制浓度
金黄色葡萄球菌
组合化学
立体化学
利血平
体外
药理学
抗生素
有机化学
生物化学
细菌
生物
遗传学
作者
François Mouton‐Liger,Pascale Bouhours,Carine Ganem‐Elbaz,Claude Jolivalt,Stéphane Pellet‐Rostaing,Florence Popowycz,Jean‐Marc Paris,Marc Lemaire
出处
期刊:ChemMedChem
[Wiley]
日期:2016-01-06
卷期号:11 (3): 320-330
被引量:21
标识
DOI:10.1002/cmdc.201500463
摘要
An innovative and straightforward synthesis of second-generation 2-arylbenzo[b]thiophenes as structural analogues of INF55 and the first generation of our laboratory-made molecules was developed. The synthesis of C2-arylated benzo[b]thiophene derivatives was achieved through a method involving direct arylation, followed by simple structural modifications. Among the 34 compounds tested, two of them were potent NorA pump inhibitors, which led to a 16-fold decrease in the ciprofloxacin minimum inhibitory concentration (MIC) against the SA-1199B strain at concentrations of 0.25 and 0.5 μg mL(-1) (1 and 1.5 μm, respectively). This is a promising result relative to that obtained for reserpine (MIC=20 μg mL(-1)), a reference compound amongst NorA pump inhibitors. These molecules thus represent promising candidates to be used in combination with ciprofloxacin against fluoroquinolone-resistant strains.
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