首页> 美国卫生研究院文献>Scientific Reports >Zephycandidine A the First Naturally Occurring Imidazo12-fphenanthridine Alkaloid from Zephyranthes candida Exhibits Significant Anti-tumor and Anti-acetylcholinesterase Activities
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Zephycandidine A the First Naturally Occurring Imidazo12-fphenanthridine Alkaloid from Zephyranthes candida Exhibits Significant Anti-tumor and Anti-acetylcholinesterase Activities

机译:Zephycandidine A第一个天然存在的天然假丝酵母咪唑并12-f菲啶生物碱具有重要的抗肿瘤和抗乙酰胆碱酯酶活性

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摘要

Zephycandidine A (1), the first naturally occurring imidazo[1,2-f]phenanthridine alkaloid, was isolated from Zephyranthes candida (Amaryllidaceae). The structure of 1 was elucidated by spectroscopic analyses and NMR calculation, and a plausible biogenetic pathway for zephycandidine A (1) was proposed. Zephycandidine A (1) exhibited significant cytotoxicity against five cancer cell lines with IC50 values ranging from 1.98 to 7.03 μM with selectivity indices as high as 10 when compared to the normal Beas-2B cell. Further studies suggested that zephycandidine A (1) induces apoptosis in leukemia cells by the activation of caspase-3, upregulation of Bax, downregulation of Bcl-2, and degradation of PARP expression. In addition, zephycandidine A (1) showed acetylcholinesterase (AChE) inhibitory activity, and the docking studies of zephycandidine A (1) and galanthamine (2) with AChE revealed that interactions with W286 and Y337 are necessary.
机译:Zephycandidine A(1)是第一个天然存在的咪唑并[1,2-f]菲啶生物碱,是从Zephyranthes candida(Amaryllidaceae)中分离出来的。通过光谱分析和NMR计算阐明了1的结构,并提出了一个有效的Zephycandidine A(1)的生物遗传途径。 Zephycandidine A(1)对五种癌细胞系表现出明显的细胞毒性,与正常的Beas-2B细胞相比,IC50值在1.98至7.03μm之间,选择性指数高达10。进一步的研究表明,zephycandidine A(1)通过激活caspase-3,Bax的上调,Bcl-2的下调以及PARP表达的降解来诱导白血病细胞凋亡。此外,zephycandidine A(1)具有乙酰胆碱酯酶(AChE)抑制活性,zephycandidine A(1)和加兰他敏(2)与AChE的对接研究表明与W286和Y337的相互作用是必要的。

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