立体化学
脚手架
细胞毒性T细胞
化学
生物
体外
工程类
生物化学
生物医学工程
作者
Shanwen Zhang,Qing Xie,Changli Sun,Xinpeng Tian,Chun Gui,Xiangjing Qin,Hua Zhang,Jianhua Ju
标识
DOI:10.1021/acs.jnatprod.9b00654
摘要
Three new kendomycin analogues, kendomycins B–D (1–3), were discovered from the marine-derived actinomycete Verrucosispora sp. SCSIO 07399. The structures of 1–3 were elucidated using diverse spectroscopic data analyses, X-ray crystallography, and semisynthetic derivatization. In vitro antimicrobial assays revealed that 1–3 all display good antibacterial activities against six Gram-positive bacteria with MIC values ranging from 0.5 to 8.0 μg/mL. Additionally, 1–3 were found to be moderately cytotoxic against MGC803, A549, HeLa, HepG2, MCF-7, and RKO human tumor cell lines; IC50 values ranged from 2.2 to 44 μM.
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