Iguchi Tomoki, Kuroda Minpei, Naito Rei, Watanabe Tomoyuki, Matsuo Yukiko, Yokosuka Akihito, Mimaki Yoshihiro
School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1, Horinouchi, Hachioji, Tokyo 192-0392, Japan.
Molecules. 2017 Jul 25;22(8):1243. doi: 10.3390/molecules22081243.
Previous phytochemical studies of the bulbs of , an ornamental perennial plant native to South Africa, resulted in the isolation of 29 new cholestane glycosides, some of which were structurally unique and showed potent cytotoxic activity against cultured tumor cell lines. Therefore, we aimed to perform further phytochemical examinations of methanolic extracts obtained from bulbs, isolating 12 new cholestane rhamnosides (-) and seven known compounds (-). The structures of the new compounds (-) were identified via NMR-based structural characterization methods, and through a sequence of chemical transformations followed by spectroscopic and chromatographic analysis. The cytotoxic activity of the isolated compounds (-) and the derivatives ( and ) against HL-60 human promyelocytic leukemia cells and A549 human lung adenocarcinoma cells was evaluated. Compounds -, , and showed cytotoxicity against both HL-60 and A549 cells. Compound showed potent cytotoxicity with an IC value of 0.16 µM against HL-60 cells and induced apoptotic cell death via a mitochondrion-independent pathway.
,一种原产于南非的观赏性多年生植物,此前对其鳞茎进行的植物化学研究分离出了29种新的胆甾烷糖苷,其中一些结构独特,对培养的肿瘤细胞系显示出强大的细胞毒性活性。因此,我们旨在对从 鳞茎中获得的甲醇提取物进行进一步的植物化学研究,分离出12种新的胆甾烷鼠李糖苷(-)和7种已知化合物(-)。通过基于核磁共振的结构表征方法,以及一系列化学转化,随后进行光谱和色谱分析,确定了新化合物(-)的结构。评估了分离出的化合物(-)及其衍生物( 和 )对HL-60人早幼粒细胞白血病细胞和A549人肺腺癌细胞的细胞毒性活性。化合物 -、 和 对HL-60和A549细胞均显示出细胞毒性。化合物 对HL-60细胞显示出强大的细胞毒性,IC值为0.16 μM,并通过非线粒体依赖性途径诱导凋亡细胞死亡。