Song Bai, Miaohe Zhang, Miao Li, Shouyin Tang, Suran Wan, Fang Wang, Xian Wei, Lijun Chen, Shuang Feng, Rong Wu
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引用次数: 0
Abstract
A series of novel coumarin derivatives have been synthesized by successfully combining the coumarin backbone with benzylamine groups using active splicing technology and chemical synthesis. These derivatives demonstrated excellent antibacterial activity in vitro with the A5 compound being particularly prominent. Through three-dimensional quantitative structure-activity relationships (3D-QSAR) analysis, it was found that the introduction of electron-donating group at the R1 position and a larger group at the R2 position could enhance the antibacterial activity, and the action mechanism of compound A5 was studied. The experimental results showed that A5 could increase the permeability of the bacterial membrane, thus disrupting the Xoo membrane and effectively inhibiting bacterial growth. This finding not only reveals the antibacterial mechanism of A5, but also provides an important scientific basis for the development of new antibacterial agents.
期刊介绍:
Chemistry & Biodiversity serves as a high-quality publishing forum covering a wide range of biorelevant topics for a truly international audience. This journal publishes both field-specific and interdisciplinary contributions on all aspects of biologically relevant chemistry research in the form of full-length original papers, short communications, invited reviews, and commentaries. It covers all research fields straddling the border between the chemical and biological sciences, with the ultimate goal of broadening our understanding of how nature works at a molecular level.
Since 2017, Chemistry & Biodiversity is published in an online-only format.