抗菌剂
吲哚试验
化学
微生物学
流出
精胺
革兰氏阴性菌
生物化学
大肠杆菌
生物
基因
酶
作者
Melissa M. Cadelis,Steven A. Li,Marie‐Lise Bourguet‐Kondracki,Marine Blanchet,Hana Douafer,Jean Michel Brunel,Brent R. Copp
出处
期刊:ChemMedChem
[Wiley]
日期:2020-10-30
卷期号:16 (3): 513-523
被引量:14
标识
DOI:10.1002/cmdc.202000359
摘要
Abstract The discovery of new antibiotic adjuvants is an attractive option for overcoming antimicrobial resistance. We have previously reported the discovery of a bis‐6‐bromoindolglyoxylamide derivative of spermine as being able to enhance the action of antibiotics against Gram‐negative bacteria but suffers from being cytotoxic and red‐blood cell haemolytic. A series of analogues was prepared exploring variation of the indolglyoxylamide unit, to include indole‐3‐acrylic, indole‐3‐acetic and indole‐3‐carboxylate units, and evaluated for antibiotic enhancing properties against a range of Gram‐negative bacteria, and for intrinsic antimicrobial, cytotoxic and haemolytic properties. Two spermine derivatives, bearing 5‐bromo‐indole‐3‐acetic acid ( 17 ) and 5‐methoxy‐indole‐3‐acrylic acid ( 14 ) end groups were found to exhibit good to moderate antibiotic adjuvant activities for doxycycline towards the Gram‐negative bacteria Pseudomonas aeruginosa , Escherichia coli and Klebsiella pneumoniae , but with more modest intrinsic antimicrobial activity and greatly reduced cytotoxic and haemolytic properties. The mechanism of action of the latter derivative identified its ability to disrupt the outer membranes of bacteria and to inhibit the AcrAB‐TolC efflux pump directly or by inhibiting the proton gradient.
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