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1.Institute of Marine Drugs, Guangxi Key Laboratory of Marine Drugs, Guangxi University of Chinese Medicine, Nanning 530200, China
An epipolythiodioxopiperazine alkaloid and diversified aromatic polyketides with cytotoxicity from the Beibu Gulf coral-derived fungus Emericella nidulans GXIMD 02509[J/OL]. 浙江大学学报(英文版)(B辑:生物医学和生物技术), 2023,1-7.
Miaoping LIN, Zhenzhou TANG, Jiaxi WANG, et al. An epipolythiodioxopiperazine alkaloid and diversified aromatic polyketides with cytotoxicity from the Beibu Gulf coral-derived fungus Emericella nidulans GXIMD 02509[J/OL]. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology), 2023,1-7.
An epipolythiodioxopiperazine alkaloid and diversified aromatic polyketides with cytotoxicity from the Beibu Gulf coral-derived fungus Emericella nidulans GXIMD 02509[J/OL]. 浙江大学学报(英文版)(B辑:生物医学和生物技术), 2023,1-7. DOI: 10.1631/jzus.ZUSB-D-22-00622-0-lhf-author.
Miaoping LIN, Zhenzhou TANG, Jiaxi WANG, et al. An epipolythiodioxopiperazine alkaloid and diversified aromatic polyketides with cytotoxicity from the Beibu Gulf coral-derived fungus Emericella nidulans GXIMD 02509[J/OL]. Journal of Zhejiang University-SCIENCE B (Biomedicine & Biotechnology), 2023,1-7. DOI: 10.1631/jzus.ZUSB-D-22-00622-0-lhf-author.
概要: 鉴定了化合物的化学结构。化合物,1,-,5,、,7,和,10,对786-O、SW1990和SW480等3株肿瘤细胞增殖具抑制活性,半抑制浓度IC,50,值为4.3–33.4 μmol/L。化合物emestrin J (,10,)具有一个二硫桥键,还能够显著抑制786-O细胞克隆及迁移,诱导786-O细胞凋亡并阻滞细胞分裂在G2/M期,是一个潜在具抗肿瘤活性的先导化合物。
巢裸胞壳菌海洋真菌芳香聚酮多硫代二酮哌嗪细胞毒
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