| Literature DB >> 20738103 |
Yoshihide Usami1, Kyoko Nakagawa-Goto, Jing-Yu Lang, Yoon Kim, Chin-Yu Lai, Masuo Goto, Nobuko Sakurai, Masahiko Taniguchi, Toshiyuki Akiyama, Susan L Morris-Natschke, Kenneth F Bastow, Gordon Cragg, David J Newman, Mihoyo Fujitake, Koichi Takeya, Mien-Chie Hung, Eva Y-H P Lee, Kuo-Hsiung Lee.
Abstract
A new quassinoid, designated 2'-(R)-O-acetylglaucarubinone (1), and seven known quassinoids (2-8) were isolated, using bioactivity-guided separation, from the bark of Odyendyea gabonensis (Pierre) Engler [syn. Quassia gabonensis Pierre]. The structure of 1 was determined by spectroscopic analysis and by semisynthesis from glaucarubolone. Complete (1)H and (13)C NMR assignments of compounds 1-8 were also established from detailed analysis of two-dimensional NMR spectra, and the reported configurations in odyendene (7) and odyendane (8) were corrected. Compound 1 showed potent cytotoxicity against multiple cancer cell lines. Further investigation using various types of breast and ovarian cancer cell lines suggested that 1 does not target the estrogen receptor or progesterone receptor. When tested against mammary epithelial proliferation in vivo using a Brca1/p53-deficient mice model, 1 also caused significant reduction in mammary duct branching.Entities:
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Year: 2010 PMID: 20738103 PMCID: PMC2954497 DOI: 10.1021/np100406d
Source DB: PubMed Journal: J Nat Prod ISSN: 0163-3864 Impact factor: 4.050