抗菌剂
灰葡萄孢菌
最小抑制浓度
环己酮
花色曲霉
镰刀菌
金黄色葡萄球菌
微生物学
天然产物
立体化学
抗菌活性
化学
生物
曲霉
细菌
植物
遗传学
作者
Sisi Liu,Rong Huang,Shou-Peng Zhang,Tangchang Xu,Kun Hu,Shao‐Hua Wu
出处
期刊:Fitoterapia
[Elsevier BV]
日期:2022-09-09
卷期号:162: 105297-105297
被引量:16
标识
DOI:10.1016/j.fitote.2022.105297
摘要
Two new nucleoside derivatives, kipukasins O (1) and P (2), one new cyclohexenone derivative, arthropsadiol D (5), and one new natural product, (+)-2,5-dimethyl-3(2H)-benzofuranone (6), together with eleven known compounds (3, 4, 7-15), were obtained from the culture broth of the endophytic fungus Aspergillus polyporicola R2 isolated from the roots of Synsepalum dulcificum. Among them, the absolute configuration of compound 5 was determined by quantum chemical calculations of NMR chemical shifts and ECD spectrum. The antimicrobial activities of these compounds were evaluated. Compound 11 exhibited obvious inhibitory activity against MRSA, Staphylococcus aureus, Salmonella typhimurium, Botrytis cinerea, and Fusarium graminearum with MIC values of 4, 4, 4, 32, and 16 μg/mL, respectively. Compound 12 exhibited antibacterial activity against S. typhimurium and MRSA with MIC values of 4 and 16 μg/mL. Compound 6 exhibited antifungal activity against F. graminearum with MIC value of 32 μg/mL.
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