Structure and cytotoxic evaluation of five 12-oxygenated eremophilanes from Ligularia lingiana

Volume: 70, Issue: 35, Pages: 5878 - 5883
Published: Sep 1, 2014
Abstract
Five new 12-oxygenated eremophilane sesquiterpenoids bearing a B-ring enone system were isolated from Ligularia lingiana S.W. Liu (Asteraceae) collected in China. Compound 5 was a Diels-Alder adduct of 3 alpha-angeloyloxy-7 beta H-8-oxoeremophila-9,11(13)-dien-12-al and the monoterpene, ocimene. Compound I showed cytotoxic activities against HeLa, HL60, Jurkat, and NIH-3T3 cells at IC50 0.0407, 0.440, 0.313, and 3.48 mu M, respectively. (C) 2014...
Paper Details
Title
Structure and cytotoxic evaluation of five 12-oxygenated eremophilanes from Ligularia lingiana
Published Date
Sep 1, 2014
Volume
70
Issue
35
Pages
5878 - 5883
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