School of Pharmaceutical Sciences, College of Medical, Pharmaceutical and Health Sciences , Kanazawa University , Kanazawa , 920-1192 , Japan.
Natural Products Research Laboratories, UNC Eshelman School of Pharmacy , University of North Carolina at Chapel Hill , Chapel Hill , North Carolina 27599-7568 , United States.
J Nat Prod. 2018 Aug 24;81(8):1884-1891. doi: 10.1021/acs.jnatprod.8b00411. Epub 2018 Aug 14.
Alangium longiflorum is currently in extinction crisis, which will likely severely hamper further phytochemical investigation of this plant species from new collections. A crude extract of leaves of A. longiflorum (N33539), collected for the U.S. National Cancer Institute in 1989, showed potent cancer cell line antiproliferative activity. A phytochemical study resulted in the isolation of 17 secondary metabolites, including two new tetrahydroisoquinoline alkaloids, 8-hydroxytubulosine (1) and 2'- O- trans-sinapoylisoalangiside (2), as well as a new sinapolyloxylupene derivative (3). Using in-house assays and NCI-60 panel screening, compound 1 displayed broad-spectrum inhibitory activity at submicromolar levels against most tested tumor cell lines, except for drug-transporter-overexpressing cells. Compound 1 caused accumulation of sub-G1 cells with no effect on cell cycle progression, suggesting that this substance is an apoptosis inducer.
冬桃目前处于灭绝危机中,这可能严重阻碍从新采集样本中对该植物物种的进一步植物化学研究。1989 年美国国家癌症研究所采集的冬桃叶粗提物(N33539)显示出对癌细胞系有很强的抗增殖活性。植物化学研究导致分离出 17 种次生代谢物,包括两种新的四氢异喹啉生物碱,8-羟基育亨宾(1)和 2'-O-反式芥子酰异阿郎碱(2),以及一种新的芥子酰氧化紫胶衍生物(3)。使用内部检测和 NCI-60 小组筛选,化合物 1 在亚微摩尔水平对大多数测试的肿瘤细胞系表现出广谱抑制活性,除了对药物转运蛋白过表达的细胞。化合物 1 引起亚 G1 期细胞的积累,对细胞周期进程没有影响,表明该物质是一种凋亡诱导剂。