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萘啶衍生物的抗菌活性。

Antimicrobial Activity of Naphthyridine Derivatives.

作者信息

Wójcicka Anna, Mączyński Marcin

机构信息

Department of Organic Chemistry and Pharmaceutical Technology, Faculty of Pharmacy, Wroclaw Medical University, 211A Borowska Str., 50-556 Wroclaw, Poland.

出版信息

Pharmaceuticals (Basel). 2024 Dec 17;17(12):1705. doi: 10.3390/ph17121705.

Abstract

To combat the problem of the increasing drug resistance of microorganisms, it is necessary to constantly search for new medicinal substances that will demonstrate more effective mechanisms of action with a limited number of side effects. Naphthyridines are N-heterocyclic compounds containing a fused system of two pyridine rings, occurring in the form of six structural isomers with different positions of nitrogen atoms, which exhibit a wide spectrum of pharmacological activity, in particular antimicrobial properties. This review presents most of the literature data about the synthetic and natural naphthyridine derivatives that have been reported to possess antimicrobial activity.

摘要

为应对微生物耐药性不断增加的问题,有必要持续寻找新的药用物质,这些物质将展现出更有效的作用机制且副作用有限。萘啶是含有两个吡啶环稠合体系的N-杂环化合物,以六种结构异构体的形式存在,氮原子位置不同,具有广泛的药理活性,尤其是抗菌特性。本综述呈现了已报道具有抗菌活性的合成和天然萘啶衍生物的大部分文献数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d22/11678664/70600908dd15/pharmaceuticals-17-01705-g001.jpg

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