Authors
Charles Gauthier, Jean Legault, Serge Lavoie, Simon Rondeau, Samuel Tremblay, André Pichette
Publication date
2009/1/23
Journal
Journal of natural products
Volume
72
Issue
1
Pages
72-81
Publisher
American Chemical Society and American Society of Pharmacognosy
Description
The naturally occurring cytotoxic saponin 28-O-β-d-glucopyranosylbetulinic acid 3β-O-α-l-arabinopyranoside (3) was easily synthesized along with seven bidesmosidic saponins starting from the lupane-type triterpenoids betulin (1) and betulinic acid (2). As highlighted by the preliminary cytotoxicity evaluation against A549, DLD-1, MCF7, and PC-3 human cancer cell lines, the bidesmosidic betulin saponin 22a, bearing α-l-rhamnopyranoside moieties at both C-3 and C-28 positions, was determined to be a potent cytotoxic agent (IC50 1.8−1.9 μM).
Total citations
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Scholar articles
C Gauthier, J Legault, S Lavoie, S Rondeau… - Journal of natural products, 2009