羟甲基
抗菌剂
海绵
立体化学
拉伤
最小抑制浓度
微生物学
化学
细菌
抗菌活性
生物
植物
遗传学
解剖
作者
Ming‐Hong Chen,Wenlong Zhang,Li Chen,Ru Lin,Yang Xie,Dongsheng Fang,Yun-Yang Lian,Hong Jiang
标识
DOI:10.1080/14786419.2018.1509333
摘要
Chemical investigation of a marine-derived actinomycete strain Verrucosispora sp. FIM06025 isolated from a marine sponge sample collected from the East China Sea, resulted in the discovery of two new alkaloids, (2-(hydroxymethyl)-3-(2-(hydroxymethyl)-3-methylaziridin-1-yl) (2-hydroxyphenyl) methanone (1) and 2-(1-hydroxyethyl)-3,4-dihydrobenzo [f] [1,4]oxazepin-5(2H)-one (2). The structures of compounds 1 and 2 were determined by the detailed analysis of 1D, 2D NMR and HR-TOF-MS data, along with literature data analysis. The bioefficacy investigations revealed that compound 1 exhibited a broad spectrum of antimicrobial activity with MIC (minimum inhibitory concentration) values ranging from 3.4 to 200 μg·mL−1 against H. pylori, P. aeroginosa, A. baumanniiin, E. coli and K. pneumonia, S. aureus, C. albicans and E. faecium, however, compound 2, up to 200 μg/mL, displayed no antibacterial activity against these bacteria.
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