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含1,2,3-三唑的杂化物对耐甲氧西林金黄色葡萄球菌(MRSA)具有潜在抗菌活性。

1,2,3-Triazole-containing hybrids with potential antibacterial activity against methicillin-resistant Staphylococcus aureus (MRSA).

作者信息

Xu Zhi

机构信息

Guizhou University of Traditional Chinese Medicine, Guiyang, 550025, PR China.

出版信息

Eur J Med Chem. 2020 Nov 15;206:112686. doi: 10.1016/j.ejmech.2020.112686. Epub 2020 Aug 5.

Abstract

Methicillin-resistant Staphylococcus aureus (MRSA), as a classic reason for genuine skin and flimsy tissues diseases, is a worldwide general wellbeing risk and has already tormented humanity for a long history, creating a critical need for the development of new classes of antibacterials. 1,2,3-Triazole moiety, readily interact with diverse enzymes and receptors in organisms through weak bond interaction, is among the most common frameworks present in the bioactive molecules. 1,2,3-Triazole derivatives, especially 1,2,3-triazole-containing hybrids, possess broad-spectrum activity against a panel of clinically important bacteria including drug-resistant pathogens, so rational design of 1,2,3-triazole derivatives may open a door for the opportunities on the development of novel anti-MRSA agents. This review is an endeavour to highlight the current scenario of 1,2,3-triazole-containing hybrids with potential anti-MRSA activity, covering articles published between 2010 and 2020.

摘要

耐甲氧西林金黄色葡萄球菌(MRSA)作为引起皮肤和软组织疾病的典型病原体,是一种全球性的公共卫生威胁,长期以来一直困扰着人类,因此迫切需要开发新型抗菌药物。1,2,3-三唑部分能够通过弱键相互作用与生物体内的多种酶和受体轻松相互作用,是生物活性分子中最常见的结构框架之一。1,2,3-三唑衍生物,尤其是含1,2,3-三唑的杂合物,对包括耐药病原体在内的一系列临床重要细菌具有广谱活性,因此合理设计1,2,3-三唑衍生物可能为新型抗MRSA药物的开发带来机遇。本综述旨在突出含1,2,3-三唑杂合物具有潜在抗MRSA活性的当前研究状况,涵盖2010年至2020年间发表的文章。

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