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Flavone glucosides from Artemisia juncea
Authors:Bakhodir S Okhundedaev  Markus Bacher  Rimma F Mukhamatkhanova  Ildar J Shamyanov  Gokhan Zengin  Stefan Böhmdorfer
Institution:1. Institute of the Chemistry of Plant Substances of the Academy Sciences of Uzbekistan, Tashkent, Uzbekistan;2. Division of Chemistry of Renewables, Department of Chemistry, University of Natural Resources and Life Sciences, Vienna (BOKU University), Tulln, Austria;3. Department of Biology, Faculty of Science, University of Selcuk, Konya, Turkey
Abstract:A new flavone glucoside, 4′,5-dihydroxy-3′,5′,6-trimethoxyflavone-7-O-β-D-glucoside was obtained from aerial parts of Artemisia juncea, together with the known flavone eupatilin (5,7-dihydroxy-3′,4′,6-trimethoxyflavone). The compounds were comprehensively analytically characterized by IR, UV, NMR and HR-MS, and their chemical structures ascertained. The EtOAc fraction of A. juncea showed the strongest DPPH radical scavenging ability as well as reducing power (in CUPRAC and FRAP assays) and phosphomolybdenum activity. This fraction also exhibited the strongest inhibitory effects on tyrosinase. Additionally, the best antidiabetic effects were observed for eupatilin and the CHCl3 fraction.
Keywords:Artemisia juncea  flavones  flavonoid  4′  5-dihydroxy-3′  5′  6-trimethoxyflavone-7-O-β-D-glucoside  eupatilin  antioxidant  enzyme inhibitor
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