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Cytotoxic sesquiterpenes from Ligularia platyglossa by Jian-Qun Liu; Mian Zhang; Chao-Feng Zhang; Huan-Yang Qi; Alan Bashall; S.W. Annie Bligh; Zheng-Tao Wang is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

What is Cytotoxic sesquiterpenes from Ligularia platyglossa about?

Four sesquiterpene lactones including an eremophilenolide dimer, named as biligulaplenolide, 1, 8bhydroxy-1-oxo-(14a,15a eremophil-7(11),9(10)-dien-12,8a-olide, 2, 1-hydroxy-2-oxo-(14a,15a eremophil-1(10),7(11),8(9)-trien-12,8-olide, 3, 4a,8b,9a-trihydroxy-5aY-7(11)-eudesmen-12,8a-olide, 4, along with two known ones, 10a-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 IC 50 in the range of 24.0 to 51.1 lM, 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.

Who reads Cytotoxic sesquiterpenes from Ligularia platyglossa?

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Jian-Qun Liu; Mian Zhang; Chao-Feng Zhang; Huan-Yang Qi; Alan Bashall; S.W. Annie Bligh; Zheng-Tao Wang
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0031-9422)
Published
2008
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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