Roy Michael C, Chang Fang-Rong, Huang Hsiao-Chu, Chiang Michael Y-N, Wu Yang-Chang
Graduate Institute of Natural Products, Kaohsiung Medical University, Kaohsiung 807, Taiwan, Republic of China.
J Nat Prod. 2005 Oct;68(10):1494-9. doi: 10.1021/np0501740.
A series of cardenolides and related compounds have been isolated from the aerial parts and roots of the ornamental milkweed, Asclepias curassavica. Their structures were determined by spectroscopic and chemical methods. Among them, three derivatives of calactinic acid methyl ester (13-15), 19-nor-16 alpha-acetoxy-10 beta-hydroxyasclepin (16), 20 beta,21-dihydroxypregna-4,6-dien-3-one (19), and 3,4-seco-urs-20(30)-en-3-oic acid (22) are new compounds. The relative configuration of calactinic acid methyl ester (12) has been confirmed by X-ray diffraction analysis on its derivative 13. Most of the cardenolides obtained showed pronounced cytotoxicity against four cancer cell lines (IC(50) 0.01 to 2.0 microg/mL).
从观赏植物马利筋(Asclepias curassavica)的地上部分和根部分离出了一系列强心甾内酯及相关化合物。通过光谱和化学方法确定了它们的结构。其中,三种卡拉actinic酸甲酯衍生物(13 - 15)、19 - 去甲- 16α-乙酰氧基- 10β-羟基马利筋苷(16)、20β,21 - 二羟基孕甾- 4,6 - 二烯- 3 - 酮(19)和3,4 - 裂环乌苏- 20(30) - 烯- 3 - 酸(22)是新化合物。通过对卡拉actinic酸甲酯(12)的衍生物13进行X射线衍射分析,证实了其相对构型。所获得的大多数强心甾内酯对四种癌细胞系显示出显著的细胞毒性(IC(50)为0.01至2.0微克/毫升)。