夫西地酸
吖啶
枯草芽孢杆菌
金黄色葡萄球菌
真菌
微生物学
抗生素
细菌
生物
立体化学
化学
植物
遗传学
作者
Chuan Tian,Han Gao,Xiao-Ping Peng,Gang Li,Hong‐Xiang Lou
标识
DOI:10.1080/10286020.2020.1866559
摘要
Fusidic acid, a representative member of fungal fusidane triterpenoids, has been clinically used as an antibiotic. In the present study, fusidic acid (1), and its known analogs 16-desacetylfusidic acid (2) and 3β,20-dihydroxy-protosta-16,24-dien-29-oic acid (4), together with one new derivative acremonidiol A (3), were isolated from the endophytic fungus, Acremonium pilosum F47. Their structures were determined by MS and NMR. The spectroscopic data of 2 are firstly reported here. The antibacterial efficacies of 1-4 were evaluated against four selected Gram-positive or Gram-negative bacteria. As expected, only compound 1 showed strong inhibitory effect on Gram-positive bacteria Staphylococcus aureus and Bacillus subtilis.
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