| Literature DB >> 18693295 |
Joo-Hee Kwon1, Min-Jung Chang, Hyo-Won Seo, Jeong-Hun Lee, Byung-Sun Min, MinKyun Na, Jin Cheol Kim, Mi Hee Woo, Jae Sue Choi, Hyeong Kyu Lee, KiHwan Bae.
Abstract
Five pentacyclic triterpenoids (1-5) and a sterol (6) were isolated from the stem-bark of Styrax japonica. The six compounds, 1-6, were determined to be 3beta-acetoxy-28-hydroxyolean-12-ene (1), 3beta-acetoxyolean-12-en-28-acid (2), 3beta-acetoxyolean-12-en-28-aldehyde (3), 3beta-acetoxy-17beta-hydroxy-28-norolean-12-ene (4), taraxerol (5) and stigmasterol (6), respectively, by spectroscopic means, including the 2D-NMR technique. Compound 4 is a newly discovered natural compound. The protein tyrosine phosphatase 1B (PTP1B) inhibitory activities of the isolated compounds (1-6) were determined in vitro. Among the isolated compounds, 3beta-acetoxyolean-12-en-28-acid (2) and 3beta-acetoxyolean-12-en-28-aldehyde (3) had the most potent inhibitory PTP1B activity, with IC50 values of 7.8 and 9.3 microm, respectively. (c) 2008 John Wiley & Sons, Ltd.Entities:
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Year: 2008 PMID: 18693295 DOI: 10.1002/ptr.2484
Source DB: PubMed Journal: Phytother Res ISSN: 0951-418X Impact factor: 5.878