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β-内酰胺酶抑制剂的最新研究进展。

Recent advances in the development of β-lactamase inhibitors.

机构信息

Department of Medicinal Chemistry, Jungwon University, Goesan, 28420, Republic of Korea.

出版信息

J Microbiol. 2020 Aug;58(8):633-647. doi: 10.1007/s12275-020-0285-z. Epub 2020 Jul 27.

Abstract

β-Lactam antibiotics are the most commonly prescribed antibiotics worldwide; however, antimicrobial resistance (AMR) is a global challenge. The β-lactam resistance in Gram-negative bacteria is due to the production of β-lactamases, including extended-spectrum β-lactamases, metallo-β-lactamases, and carbapenem-hydrolyzing class D β-lactamases. To restore the efficacy of BLAs, the most successful strategy is to use them in combination with β-lactamase inhibitors (BLI). Here we review the medically relevant β-lactamase families and penicillins, diazabicyclooctanes, boronic acids, and novel chemical scaffold-based BLIs, in particular approved and under clinical development.

摘要

β-内酰胺类抗生素是全球应用最广泛的抗生素;然而,抗菌药物耐药性(AMR)是一个全球性挑战。革兰氏阴性菌的β-内酰胺类抗生素耐药性是由于β-内酰胺酶的产生,包括超广谱β-内酰胺酶、金属β-内酰胺酶和碳青霉烯水解酶 D 类β-内酰胺酶。为了恢复 BLAs 的疗效,最成功的策略是将它们与β-内酰胺酶抑制剂(BLI)联合使用。在这里,我们综述了与医学相关的β-内酰胺酶家族和青霉素、二氮杂双环辛烷、硼酸和新型基于化学结构骨架的 BLIs,特别是已批准和正在临床开发中的药物。

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