Chem. J. Chinese Universities ›› 2006, Vol. 27 ›› Issue (5): 859.

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Sesquiterpene Lactones from Cyathocline purpurea

LI Zu-Qiang1*, MA Guo-Yi2, LUO Lei3, ZHANG Xi-Tai2   

  1. 1. Experimental Center, College of Chemistry and Material Engineering, Yunnan University, Kunming 650091, China;
    2. Faculty of Pharmacy, the University of Sydney, NSW, Australia;
    3. Chemical & Engineering College, Yunnan Normal University, Kunming 650092, China
  • Received:2005-06-29 Online:2006-05-10 Published:2006-05-10
  • Contact: LI Zu-Qiang, E-mail: ZuqiangLi@ynu.edu.cn

Abstract:

Cyathocline purpurea(Buch-Ham ex D Don) O Ktze is a folk drug used to treat inflammations and pulmonary tuberculosis in Yunnan Province. Cytotoxicity screening of extracts and its fractions from C. purpurea was carried out by L1210 cell. Isolation of chemical constituents by column chromatography was undertaken in step with cytotoxicity test. The structures of constituents were identified by spectroscopic and chemical methods. The chloroform and ethyl acetate extracts possess cytotoxic activity with IC50′s being 3.5 and 2.8 μg/mL, respectively. Three sesquiterpene lactones were established as Santamarin(compound 1), 9β-acetoxycostunolide(compound 2) and 9β-acetoxypathenolide(compound 3). Their IC50 were 0.41, 0.89, 0.59 μg/mL by L1210 cell respectively. The three constituents were obtained for the first time from this plant. They are all anticancer active constituents. The last one is a new compound.

Key words: Cyathocline purpurea; Cytotoxicity; Sesquiterpene lactone; 9β-Acetoxycostunolide; 9β-Acetoxypathenolide

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