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Anticomplementary activity of stilbenes from medicinal plants
Authors:Sei-Ryang Oh  Shi Yong Ryu  Si Hyung Park  Keun Young Jung  Im Seon Lee  Kyung Seop An  Jung Joon Lee  Hyeong-Kyu Lee
Affiliation:(1) Korea Research Institute of Bioscience & Biotechnology, KIST, Yusong, P.O. Box 115, 305-600 Taejon, Korea;(2) Korea Research Institute of Chemical Technology, 305-606 Taejon, Korea
Abstract:
The anticomplementary activity of stilbenes from medicinal plants in Korea was investigatedin vitro. 3,5-Dihydroxy-4′-methoxystilbene (3) was most potent with IC50 value of 1.5×10−4 M followed by rhapontigenin (4), oxyresverastrol (2), 2,3,4′,5-tetrahydroxystilbene-2-O-β-glucoside (9), rhaponticin (8), resverastrol (1), and piceid (7). The activity was found to be increased by a methylation on a hydroxy group of C-4′ of1, but decreased by further methylation on hydroxy groups of C-3 and C-5 and glucosylation on any hydroxy group of1. Addition of hydroxy group on C-2′ of1 or C-3′ of3 was little affected on the anticomplementary activity but the activity was increased byO-glucosylation on C-2 of1.
Keywords:Anticomplementary activity  Stilbenes  Resveratrol  Oxyresveratrol  3,5-Dihydroxy-4-methoxystilbene  Rhapontigenin  Rhaponticin  Piceid  2,3,4′  ,5-Tetrahydroxy stilbene-2-O  -glucoside  2,3,4′  ,5-Tetrahydroxystilbene-2-O  -glucosyl-4′  -O  -gluco-side
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