赫拉
生物碱
真菌
二维核磁共振波谱
立体化学
K562细胞
曲霉
生物
细胞毒性T细胞
癌细胞系
化学
生物化学
植物
癌细胞
细胞
癌症
体外
遗传学
作者
Siwen Niu,Ziming Chen,Shengxiang Pei,Zongze Shao,Gaiyun Zhang,Bihong Hong
标识
DOI:10.1080/14786419.2021.1913587
摘要
Chemical investigation of the deep-sea-derived fungus Aspergillus sydowii MCCC 3A00324 led to the isolation of one new acremolin type alkaloid (acremolin D, 1) and five known alkaloids (2‒6). The planar structure of 1 was established by the extensive analyses of the NMR and HRESIMS data, while its absolute configuration was assigned by the comparison of the experimental and calculated ECD data. Acremolin D (1) represented the second analogue of acremolin found in nature. All compounds were evaluated for their cytotoxic activities against six human cancer cell lines (A549, Hela-S3, MCF-7, HepG2, K562, and SF-268). As a result, compounds 1 and 2 exhibited a certain inhibitory effects against the proliferation of the A549, Hela-S3, HepG2, and K562 cell lines at the concentration of 20 µM.[Formula: see text].
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