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廖尚高, 王珍, 李靖, 刘影, 李月婷, 张丽娟, 龙庆德, 王永林. 南川斑鸠菊中的抗肿瘤倍半萜内酯[J]. 中国天然药物, 2012, 10(3): 230-233.
引用本文: 廖尚高, 王珍, 李靖, 刘影, 李月婷, 张丽娟, 龙庆德, 王永林. 南川斑鸠菊中的抗肿瘤倍半萜内酯[J]. 中国天然药物, 2012, 10(3): 230-233.
LIAO Shang-Gao, WANG Zhen, LI Jing, LIU Ying, LI Yue-Ting, ZHANG Li-Juan, LONG Qing-De, WANG Yong-Lin. Cytotoxic sesquiterpene lactones from Vernonia bockiana[J]. Chinese Journal of Natural Medicines, 2012, 10(3): 230-233.
Citation: LIAO Shang-Gao, WANG Zhen, LI Jing, LIU Ying, LI Yue-Ting, ZHANG Li-Juan, LONG Qing-De, WANG Yong-Lin. Cytotoxic sesquiterpene lactones from Vernonia bockiana[J]. Chinese Journal of Natural Medicines, 2012, 10(3): 230-233.

南川斑鸠菊中的抗肿瘤倍半萜内酯

Cytotoxic sesquiterpene lactones from Vernonia bockiana

  • 摘要: 目的:研究南川斑鸠菊中的抗肿瘤活性成分方法:采用层析柱和制备高效液相进行化合物分离,运用1H和13C NMR及MS等波谱分析技术鉴定化合物结构;采用MTT法进行7个化合物对人骨髓白血病细胞(HL-60)的体外细胞毒实验。结果:分离得到6个倍半萜内酯8-(4-hydroxymethacryloyloxy)-10-hydroxy-13-methoxyhirsutinolide (1), 8-methacryloyloxy-10-hydroxy-13-O-methylhirsutinolide (2), piptocarphin A (3), 8-4-hydroxymethacryloyloxy-10-hydroxyhisutinolide-13-O-acetate (4), piptocarphin F (5)以及8-acetoxy-10-hydroxy-13-O-methylhirsutinolide (6)和1个inone苷saussureosides B (7); 6个倍半萜内酯(1-6)具有抑制人骨髓白血病细胞(HL-60)的活性(IC503.87-12.5molL-1),但inone苷saussureosides B (7)对HL-60没有抑制活性。结论:化合物1, 2, 6和7首次从该植物中得到;南川斑鸠菊中的倍半萜内酯类化合物具有抗肿瘤活性。

     

    Abstract: AIM: To investigate antitumor compounds from Vernonia bockiana. METHODS: The compounds were isolated by column chromatography and preparative HPLC. Their structures were elucidated by 1H and 13C NMR spectroscopic methods and MS experiments. The antitumor activity was evaluated by testing their cytotoxicity against the human promyelomonocyte leukemic cell line HL-60 by the MTT method. RESULTS: Six sesquiterpene lactones, 8-(4-hydroxymethacryloyloxy)-10-hydroxy-13-methoxyhirsutinolide (1), 8-methacryloyloxy-10-hydroxy-13-O-methylhirsutinolide (2), piptocarphin A (3), 8-4-hydroxymethacryloyloxy- 10-hydroxyhisutinolide-13-O-acetate (4), piptocarphin F (5), and 8-acetoxy-10-hydroxy-13-O-methylhirsutinolide (6), and one known inone glycoside, saussureosides B (7), were isolated from the whole plant of V. bockiana. The six sesquiterpene lactones showed cytotoxic activity (IC50 3.87-12.5 molL-1) against the human leukemic cell line HL-60 while the inone glycoside 7 was inactive in the test. CONCLUSION: Compounds 1, 2, 6, and 7 were obtained for the first time from this plant; The sesquiterpene lactones present in V. bockiana were active as antitumor agents against the human leukemic cell line HL-60.

     

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