Flavone glucosides from <i>Artemisia juncea</i> release_dcd7zr5vzveqjpqpuscissabq4

by Bakhodir S. Okhundedaev, Markus Bacher, Rimma F. Mukhamatkhanova, Ildar J. Shamyanov, Gokhan Zengin, Stefan Böhmdorfer, Nilufar Z. Mamadalieva, Thomas Rosenau

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abstracts [{'sha1': '3e5bb0dd0abe25ca93d1389a8ea0ffb8873666f6', 'content': 'A new flavone glucoside, 4′,5-dihydroxy-3′,5′,6-trimethoxyflavone-7-<i>O</i>-β-D-glucoside was obtained from aerial parts of <i>Artemisia juncea</i>, 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 <i>A. juncea</i> 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 CHCl<sub>3</sub> fraction.', 'mimetype': 'text/plain', 'lang': 'en'}]
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release_date 2018-11-13
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release_type article-journal
release_year 2018
revision e0e49bd2-a99c-4bfe-85b5-59266e2a6546
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title Flavone glucosides from <i>Artemisia juncea</i>
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datacite.subjects [{'subject': 'Biochemistry'}, {'subject': 'Genetics'}, {'subject': 'Physiology'}, {'subject': 'Pharmacology'}, {'schemeUri': 'http://www.abs.gov.au/ausstats/abs@.nsf/0/6BB427AB9696C225CA2574180004463E', 'subject': '39999 Chemical Sciences not elsewhere classified', 'subjectScheme': 'FOR'}, {'subject': 'Sociology'}, {'subject': 'Hematology'}]
release_month 11