H.E.J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi 75270, Pakistan.
Phytochemistry. 2010 Dec;71(17-18):2205-9. doi: 10.1016/j.phytochem.2010.08.019. Epub 2010 Oct 31.
Phytochemical studies on the aerial parts of Withania somnifera L. Dunal. (Solanaceae) led to the isolation of a chlorinated steroidal lactone (27-acetoxy-4β,6α-dihydroxy-5β-chloro-1-oxowitha-2,24-dienolide), a diepoxy withanolide (5β,6β,14α,15α-diepoxy-4β,27-dihydroxy-1-oxowitha-2,24-dienolide), and withaferin A. Their structures were elucidated by using spectroscopic techniques. All three compounds exhibited a growth inhibition and cytotoxic activity against human lung cancer cell line (NCI-H460), with withaferin A being the most potent (GI(50)=0.18 μg/mL and LC(50)=0.45 μg/mL) among three compounds tested.
从睡茄(茄科)的地上部分的植物化学研究中分离得到一个氯化甾体内酯(27-乙酰氧基-4β,6α-二羟基-5β-氯-1-氧代沃塔-2,24-二烯醇内酯),一个双环氧醇(5β,6β,14α,15α-双环氧-4β,27-二羟基-1-氧代沃塔-2,24-二烯醇内酯)和沃塔林 A。通过光谱技术阐明了它们的结构。所有三种化合物均对人肺癌细胞系(NCI-H460)表现出生长抑制和细胞毒性活性,其中沃塔林 A 的活性最强(GI(50)=0.18μg/mL,LC(50)=0.45μg/mL)。