Zhang Yao-Chun, Zhou Liang, Ng Ka-Yun
Department of Pharmacy, National University of Singapore, Singapore, Singapore.
J Asian Nat Prod Res. 2009;11(4):294-8. doi: 10.1080/10286020902727520.
A new sesquiterpene lactone glucoside, 11,13-dihydroixerinoside (1), together with the five known sesquiterpene lactones, ixerinoside (2), ixerin Z (3), 11,13alpha-dihydroixerin Z (4), ixerin Z1 (5), and 3-hydroxydehydroleucodin (6), respectively, were isolated from the whole plants of Ixeris sonchifolia Hance. The compounds were identified by spectral analysis and comparison with spectroscopic data reported in the literatures. When the in vitro cytotoxic activities of compounds 1-6 were evaluated against A549 human non-small cell lung cancer cells, all six compounds exhibited cytotoxic activity against A549 cells, with compounds 2, 3, and 6 showing good activities (inhibitory concentration (IC(50) values < 30 microg/ml) that are comparable with well-established chemotherapeutic drug, 5-fluorouracil.
从苦荬菜全草中分别分离得到一种新的倍半萜内酯苷,11,13 - 二氢苦荬菜苷(1),以及五种已知的倍半萜内酯,即苦荬菜苷(2)、苦荬菜素Z(3)、11,13α - 二氢苦荬菜素Z(4)、苦荬菜素Z1(5)和3 - 羟基脱氢亮叶桉内酯(6)。通过光谱分析并与文献报道的光谱数据进行比较对这些化合物进行了鉴定。当评估化合物1 - 6对A549人非小细胞肺癌细胞的体外细胞毒活性时,所有六种化合物均对A549细胞表现出细胞毒活性,其中化合物2、3和6显示出良好的活性(抑制浓度(IC(50)值< 30μg/ml),与成熟的化疗药物5 - 氟尿嘧啶相当。