Literature DB >> 17970595

Cytotoxic sesquiterpene lactones from Pseudoelephantopus spicatus.

Yu-Liang Yang1, Sue-Ming Chang, Ching-Chung Wu, Pei-Wen Hsieh, Shu-Li Chen, Fang-Rong Chang, Wen-Chun Hung, Hamad H Issa, Yang-Chang Wu.   

Abstract

Five new sesquiterpene lactones, spicatolides D-H (1-5), along with four known compounds, pitocarphin D (6), 8 alpha-acetoxy-10 alpha-hydroxy-13-O-methylhirsutinolide (7), spicatolide A (8), and 13-O-methylvernojalcanolide 8-O-acetate (9), were isolated from an ethyl acetate extract of the aerial parts of Pseudoelephantopus spicatus. The structures of the new compounds were elucidated on the basis of spectroscopic data interpretation. All of the compounds isolated were evaluated for their cytotoxic effects against five human cancer cell lines. Compounds 1, 3, and 4 showed cytotoxicity (IC50 < 5 micro g/mL) against the Hep3B and MCF-7 cancer cell lines.

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Year:  2007        PMID: 17970595     DOI: 10.1021/np070331q

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  1 in total

1.  Toward an integrated route to the vernonia allenes and related sesquiterpenoids.

Authors:  Da Xu; Michael A Drahl; Lawrence J Williams
Journal:  Beilstein J Org Chem       Date:  2011-07-05       Impact factor: 2.883

  1 in total

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