Cytotoxic sesquiterpenes from Ligularia platyglossa

Liu, Jian-Qun, Zhang, Mian, Zhang, Chao-Feng, Qi, Huan-Yang, Bashall, Alan, Bligh, S.W. Annie and Wang, Zhengtao (2008) Cytotoxic sesquiterpenes from Ligularia platyglossa. Phytochemistry, 69 (11). pp. 2231-2236. ISSN 0031-9422

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Official URL: http://dx.doi.org/10.1016/j.phytochem.2008.05.018

Abstract

Four sesquiterpene lactones including an eremophilenolide dimer, named as biligulaplenolide, 1, 8?-hydroxy-1-oxo-(14?,15? eremophil-7(11),9(10)-dien-12,8?-olide, 2, 1-hydroxy-2-oxo-(14?,15? eremophil-1(10),7(11),8(9)-trien-12,8-olide, 3, 4?,8?,9?-trihydroxy- 5??-7(11)-eudesmen-12,8?-olide, 4, along with two known ones, 10?-hydroxy-1-oxo-eremophil-7(11),8(9)-dien-12,8-olide, 5, and furanoeremophil-1(10)-ene-2,9-dione, 6, were isolated from the underground organs of Ligularia platyglossa (Franch.) Hand.-Mazz. Their structures were elucidated by spectroscopic methods including single-crystal X-ray diffraction analysis (2 and 3). Their in vitro cytotoxicities against seven cancer cell lines (BGC-823, A549, HL-60, B16, SMMC-7721, BEL7402, Hela) were evaluated. Compounds 2, 3, 5 showed cytotoxic activities on HL-60 cancer cells with IC50 in the range of 24.0 to 51.1 ?M, whereas compound 3 exhibited only weak cytotoxic activity against the B16, BEL7402 and Hela cancer cells. Flow cytometric analysis indicated that compound 3 induces Hela cells to apoptotic death after 48 h treatment with 0.38 mM of this compound.

Item Type: Article
Subjects: University of Westminster > Science and Technology > Life Sciences, School of (No longer in use)
Depositing User: Rachel Wheelhouse
Date Deposited: 25 Feb 2013 13:29
Last Modified: 25 Feb 2013 13:29
URI: http://westminsterresearch.wmin.ac.uk/id/eprint/12166

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