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分子杂交策略设计的喹诺酮类抗菌化合物进展

宋润喆 郑刚

石油化工2024,Vol.53Issue(12):1827-1835,9.
石油化工2024,Vol.53Issue(12):1827-1835,9.DOI:10.3969/j.issn.1000-8144.2024.12.020

分子杂交策略设计的喹诺酮类抗菌化合物进展

Progress in the design of quinolone antibacterial compounds based on molecular hybridization strategy

宋润喆 1郑刚1

作者信息

  • 1. 中石化(北京)化工研究院有限公司,北京 100013
  • 折叠

摘要

Abstract

Quinolone compounds are widely used in the clinical treatment of bacterial infections,and some quinolone derivatives are the first choice for treating specific infections.With the long-term use of antibacterial agents,it is necessary to develop antibacterial agents with new structures.The molecular hybridization strategy was adopted to combine two bioactive fragments to obtain new compounds with higher target activities or multiple targets to improve the overall activities of agents in vivo to the disease and achieve better effects.This paper reviewed the mechanism of action and structure-activity relationship of quinolones,the progress in novel quinolone antibacterial compounds obtained by the molecular hybridization strategy,and the research progress in the optimization of quinolone antibacterial compounds.

关键词

喹诺酮类/抗菌/分子杂交

Key words

quinolone/antibacterial/molecular hybridization

分类

化学化工

引用本文复制引用

宋润喆,郑刚..分子杂交策略设计的喹诺酮类抗菌化合物进展[J].石油化工,2024,53(12):1827-1835,9.

石油化工

OA北大核心CSTPCD

1000-8144

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