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噁唑烷酮:一种有前途的抗菌药物开发骨架。

Oxazolidinone: A promising scaffold for the development of antibacterial drugs.

机构信息

Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, Zhengzhou, 450018, China; School of Pharmaceutical Sciences & Key Laboratory of Advanced Drug Preparation Technologies, Zhengzhou University, Zhengzhou, 450001, China.

Department of Obstetrics and Gynecology, Zhengzhou Key Laboratory of Endometrial Disease Prevention and Treatment Zhengzhou China, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, China.

出版信息

Eur J Med Chem. 2023 Mar 15;250:115239. doi: 10.1016/j.ejmech.2023.115239. Epub 2023 Mar 1.

Abstract

Due to the long-term and widespread use of antibiotics in clinic, the problem of bacterial resistance is increasingly serious, and the development of new drugs to treat drug-resistant bacteria has gradually become the mainstream direction of antibiotic research. The oxazolidinone-containing drugs linezolid, tedizolid phosphate and contezolid have been approved to the market, which are effective against a variety of Gram-positive bacterium infections. Moreover, there are also many antibiotics containing oxazolidinone fragment under clinical investigation that show good pharmacokinetic and pharmacodynamic properties with unique mechanism of action against resistant bacteria. In this review, we summarized the oxazolidinone-based antibiotics already on the market or in clinical trials and the representative bioactive molecules, and mainly focused on their structural optimizations, development strategies and structure-activity relationships in hope of insight into the reasonable design for medical chemists to develop new oxazolidinone antibiotics with highly potency and fewer side effects.

摘要

由于抗生素在临床上的长期广泛使用,细菌耐药问题日益严重,开发治疗耐药菌的新药逐渐成为抗生素研究的主流方向。含恶唑烷酮的药物利奈唑胺、替地唑胺磷酸盐和康替唑胺已获准上市,可有效治疗多种革兰氏阳性菌感染。此外,还有许多含有恶唑烷酮片段的抗生素正在临床研究中,它们具有独特的作用机制,对耐药菌具有良好的药代动力学和药效学特性。本综述总结了已上市或处于临床试验阶段的基于恶唑烷酮的抗生素以及代表性的生物活性分子,并主要关注它们的结构优化、开发策略和构效关系,以期为医学化学家合理设计具有高效、低副作用的新型恶唑烷酮抗生素提供思路。

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