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Protein Tyrosine Phosphatase 1B inhibitory Activity of Anthraquinones and Stilbenes  

Na, Min-Kyun (College of Pharmacy, Yeungnam University)
Jin, Wen Yi (College of Pharmacy, Chungnam National University)
Min, Byung-Sun (College of Pharmacy, Catholic University of Daegu)
Ahn, Jong-Seog (Korea Research Institute of Bioscience and Biotechnology (KRIBB),)
Bae, Ki-Hwan (College of Pharmacy, Chungnam National University)
Publication Information
Natural Product Sciences / v.14, no.2, 2008 , pp. 143-146 More about this Journal
Abstract
Protein tyrosine phosphatase 1B (PTP1B) is emerging as a potential therapeutic target for the treatment of type-2 diabetes and obesity. To search for new types of PTP1B inhibitors, we have undertaken in vitro enzyme assay for some anthraquinones and stilbenes isolated from plants. Of the anthraquinones tested, physcion (1), 1-O-methylemodin (2), and emodin (3) showed high activities, with $IC_{50}$ values of 7.6, 7.0, and $3.8{\mu}g/mL$, respectively, while the anthraquinone glycosides, physcion-8-O-${\beta}$-D-glucopyranoside (4) and emodin-8- O-${\beta}$-D-glucopyranoside (5), were less active than their aglycones. All the stilbenens (6 - 15) slightly inhibited PTP1B activity at high concentration of $30{\mu}g/mL$. Our findings suggest that the hypoglycemic effect of anthraquinones may be associated with their PTP1B inhibitory activity.
Keywords
Protein tyrosine phosphatase 1B (PTP1B); anthraquinones; stilbenes; in vitro enzyme assay;
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Times Cited By KSCI : 3  (Citation Analysis)
Times Cited By SCOPUS : 1
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