Anticomplementary activity of stilbenes from medicinal plants |
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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 |
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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 |
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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. |
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Keywords: | Anticomplementary activity Stilbenes Resveratrol Oxyresveratrol 3,5-Dihydroxy-4-methoxystilbene Rhapontigenin Rhaponticin Piceid 2,3,4′ ,5-Tetrahydroxy stilbene-2-O-β -glucoside 2,3,4′ ,5-Tetrahydroxystilbene-2-O-β -glucosyl-4′ -O-β -gluco-side |
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