Zhan Guanqun, Qu Xiaolan, Liu Junjun, Tong Qingyi, Zhou Junfei, Sun Bin, Yao Guangmin
Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
School of Pharmaceutical Sciences, Taishan Medical University, Tai-An 271016, People's Republic of China.
Sci Rep. 2016 Sep 23;6:33990. doi: 10.1038/srep33990.
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 IC 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.
泽菲卡定碱A(1)是从葱莲(石蒜科)中分离得到的首个天然存在的咪唑并[1,2-f]菲啶生物碱。通过光谱分析和核磁共振计算阐明了1的结构,并提出了泽菲卡定碱A(1)可能的生物合成途径。泽菲卡定碱A(1)对五种癌细胞系表现出显著的细胞毒性,IC值范围为1.98至7.03 μM,与正常的Beas-2B细胞相比,选择性指数高达10。进一步的研究表明,泽菲卡定碱A(1)通过激活半胱天冬酶-3、上调Bax、下调Bcl-2以及降解PARP表达来诱导白血病细胞凋亡。此外,泽菲卡定碱A(1)显示出乙酰胆碱酯酶(AChE)抑制活性,泽菲卡定碱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。