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高效小分子氨基喹啉醌类化合物抗耐药 和 。

Highly Active Small Aminated Quinolinequinones against Drug-Resistant and .

机构信息

Department of Chemistry, Engineering Faculty, Istanbul University-Cerrahpasa, Avcilar, Istanbul 34320, Turkey.

Department of Chemistry, Gebze Technical University, Gebze, Kocaeli 41400, Turkey.

出版信息

Molecules. 2022 May 3;27(9):2923. doi: 10.3390/molecules27092923.

Abstract

Two subseries of aminated quinolinequinones (AQQs, -) containing electron-withdrawing group (EWG) or electron-donating group (EDG) in aryl amine moiety were successfully synthesized. Antimicrobial activity assessment indicates that some of the AQQs (- and -) with an EDG in aryl amine exhibited strong antibacterial activity against Gram-positive bacterial strains, including Staphylococcus aureus (ATCC 29213) and Enterococcus faecalis (ATCC 29212). In contrast, with an EWG in aryl amine displayed excellent antifungal activity against fungi Candida albicans (ATCC 10231) with a MIC value of 1.22 μg/mL. To explore the mode of action, the selected AQQs ( and ) were further evaluated in vitro to determine their antimicrobial activity against each of 20 clinically obtained resistant strains of Gram-positive bacteria by performing antibiofilm activity assay and time-kill curve assay. In addition, in silico studies were carried out to determine the possible mechanism of action observed in vitro. The data obtained from these experiments suggests that these molecules could be used to target pathogens in different modes of growth, such as planktonic and biofilm.

摘要

成功合成了两个含吸电子基团(EWG)或供电子基团(EDG)的氨基喹啉醌(AQQ)亚系列。抗菌活性评估表明,一些在芳胺部分具有 EDG 的 AQQ(-和-)对革兰氏阳性菌菌株具有很强的抗菌活性,包括金黄色葡萄球菌(ATCC 29213)和粪肠球菌(ATCC 29212)。相比之下,在芳胺部分具有 EWG 的 显示出对真菌白色念珠菌(ATCC 10231)的优异抗真菌活性,MIC 值为 1.22 μg/mL。为了探索作用模式,进一步评估了选定的 AQQ(和)在体外对 20 种临床获得的耐革兰氏阳性菌进行抗生物膜活性测定和时间杀伤曲线测定,以确定它们对每种耐药菌株的抗菌活性。此外,还进行了计算机研究以确定体外观察到的可能作用机制。这些实验获得的数据表明,这些分子可用于以不同的生长模式靶向病原体,例如浮游生物和生物膜。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439a/9104734/ce6a956f80c2/molecules-27-02923-g001.jpg

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