化学
天然产物
系列(地层学)
抗真菌
化学合成
抗菌剂
生物活性
组合化学
产品(数学)
广谱
肽
立体化学
结构-活动关系
集合(抽象数据类型)
肽合成
有机化学
生物系统
生化工程
铅化合物
生物化学
作者
Raghu Bolisetti,Karl A. Hansford,Johannes Zuegg,Alysha G. Elliott,Louise I. M. Friberg,M Cooper,Mark A. T. Blaskovich
标识
DOI:10.1021/acs.jmedchem.5c02335
摘要
The octapeptins are a set of 18 closely related natural product cyclic lipopeptides with broad spectrum activity against Gram-negative bacteria, including polymyxin-resistant strains. Within this class, only four congeners have been synthesized and/or tested in pure form, prompting us to investigate all 18 individual members. Here, we describe their chemical synthesis, which required the preparation of a series of chiral β-hydroxy fatty acids followed by solid-phase peptide synthesis and solution-phase cyclization. The series was tested against a panel of polymyxin-sensitive and -resistant Gram-negative pathogens, with minimum inhibitory concentrations of 2-8 μg/mL for most members. Oct-B5 and Oct-C0, two analogues possessing structural features disparate from those of the rest of the series, were shown to be inactive against the same panel of bacteria. Antifungal activity was also tested. This study demonstrates the first systematic synthesis and antimicrobial testing of a complete set of octapeptin natural product lipopeptides.
科研通智能强力驱动
Strongly Powered by AbleSci AI