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针对生物膜形成的抗菌剂的发现:amycolasporins 的全合成与研究。

Discovery of antibacterial agents targeting biofilm formation: total synthesis and investigation of amycolasporins.

机构信息

Institute of Microbial Pharmaceuticals, College of Life and Health Sciences, Northeastern University, Shenyang 110819, China.

出版信息

Org Biomol Chem. 2022 Aug 31;20(34):6831-6843. doi: 10.1039/d2ob01166b.

Abstract

Three monoterpene alkaloids amycolasporin A and (±) amycolasporins B and C have been synthesized for the first time from commercially available materials in yields of 31%, 14% and 21%, respectively. Their six analogues (18, 19, 30a and 30d-30f) were synthesized through a similar protocol. Meanwhile, the antibacterial activity of all synthesized molecules was evaluated, showing different levels of bioactivity. Among them, analogue 30d was screened as the most effective antibacterial candidate against (MIC value, 12.5 μg mL) and . (MIC value, 12.5 μg mL). Further investigation showed that 30d obviously inhibited biofilm formation and disrupted the preformed biofilm of . and . by promoting intracellular ROS release.

摘要

三种单萜生物碱 amycolasporin A 和(±)amycolasporins B 和 C 首次从商业可得的材料中以 31%、14%和 21%的产率合成。它们的六个类似物(18、19、30a 和 30d-30f)通过类似的方案合成。同时,评估了所有合成分子的抗菌活性,显示出不同水平的生物活性。其中,类似物 30d 被筛选为针对 (MIC 值,12.5 μg mL)和 的最有效抗菌候选物。进一步的研究表明,30d 通过促进细胞内 ROS 释放,明显抑制 生物膜的形成并破坏 生物膜的形成。

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