Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/58328
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dc.contributor.authorWongvarit Panidthananonen_US
dc.contributor.authorTanawat Chaowaskuen_US
dc.contributor.authorBoonchoo Sritularaken_US
dc.contributor.authorKittisak Likhitwitayawuiden_US
dc.date.accessioned2018-09-05T04:22:46Z-
dc.date.available2018-09-05T04:22:46Z-
dc.date.issued2018-01-01en_US
dc.identifier.issn14203049en_US
dc.identifier.other2-s2.0-85049451194en_US
dc.identifier.other10.3390/molecules23071600en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85049451194&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/58328-
dc.description.abstract© 2018 by the authors. Phytochemical investigations of the leaves and stems of Pseuduvaria fragrans led to the isolation of a new benzophenone C-glucoside named pseuduvarioside (1), together with six known compounds including (−)-guaiol (2), (+)-isocorydine (3), cyathocaline (4), isoursoline (5), N-trans-coumaroyltyramine (6), and N-trans-feruloyltyramine (7). Their structures were characterized by NMR spectroscopy and mass spectrometry. All of the isolates were evaluated for inhibitory activity against the enzyme α-glucosidase. N-trans-coumaroyltyramine and N-trans-feruloyltyramine showed higher activity than the drug acarbose. Kinetic studies revealed that both tyramine-derived amides were uncompetitive inhibitors of the enzyme.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleA new benzophenone C-glucoside and other constituents of pseuduvaria fragrans and their α-glucosidase inhibitory activityen_US
dc.typeJournalen_US
article.title.sourcetitleMoleculesen_US
article.volume23en_US
article.stream.affiliationsChulalongkorn Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
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