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CHEN Wei, LUO Xiao-Hua, WANG Zhuo, ZHANG Ying-Ying, LIU Li-Ping, WANG Hong-Bing. A new biflavone glucoside from the roots of Stellera chamaejasme[J]. 中国天然药物, 2015, 13(7): 550-553.
引用本文: CHEN Wei, LUO Xiao-Hua, WANG Zhuo, ZHANG Ying-Ying, LIU Li-Ping, WANG Hong-Bing. A new biflavone glucoside from the roots of Stellera chamaejasme[J]. 中国天然药物, 2015, 13(7): 550-553.
CHEN Wei, LUO Xiao-Hua, WANG Zhuo, ZHANG Ying-Ying, LIU Li-Ping, WANG Hong-Bing. A new biflavone glucoside from the roots of Stellera chamaejasme[J]. Chinese Journal of Natural Medicines, 2015, 13(7): 550-553.
Citation: CHEN Wei, LUO Xiao-Hua, WANG Zhuo, ZHANG Ying-Ying, LIU Li-Ping, WANG Hong-Bing. A new biflavone glucoside from the roots of Stellera chamaejasme[J]. Chinese Journal of Natural Medicines, 2015, 13(7): 550-553.

A new biflavone glucoside from the roots of Stellera chamaejasme

A new biflavone glucoside from the roots of Stellera chamaejasme

  • 摘要: The present study investigated the chemical constituents of the roots of Stellera chamaejasme (Thymelaeaceae). One new biflavone glucoside (1), along with other thirteen known compounds (2-14), was isolated by repeated column chromatographic methods and their structures were elucidated on the basis of spectral analyses. The cytotoxic activities of selected compounds were evaluated against four human cancer cell lines (A549, BEL-7402, HCT-116, and MDA-MB-231) by the SRB assay method. Compound 9 showed remarkable cytotoxicity against BEL-7402 with IC50 value being 0.65 gmL-1; compounds 7, 8, and 12 exhibited significant cytotoxic activity against A549 with IC50 values being 2.38, 1.57, and 2.35 gmL-1, respectively.

     

    Abstract: The present study investigated the chemical constituents of the roots of Stellera chamaejasme (Thymelaeaceae). One new biflavone glucoside (1), along with other thirteen known compounds (2-14), was isolated by repeated column chromatographic methods and their structures were elucidated on the basis of spectral analyses. The cytotoxic activities of selected compounds were evaluated against four human cancer cell lines (A549, BEL-7402, HCT-116, and MDA-MB-231) by the SRB assay method. Compound 9 showed remarkable cytotoxicity against BEL-7402 with IC50 value being 0.65 gmL-1; compounds 7, 8, and 12 exhibited significant cytotoxic activity against A549 with IC50 values being 2.38, 1.57, and 2.35 gmL-1, respectively.

     

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