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dc.contributor.authorIttipon Siridechakornen_US
dc.contributor.authorWisanu Maneeraten_US
dc.contributor.authorTawanun Sripisuten_US
dc.contributor.authorThunwadee Ritthiwigromen_US
dc.contributor.authorSarot Cheenprachaen_US
dc.contributor.authorSurat Laphookhieoen_US
dc.date.accessioned2018-09-04T09:44:18Z-
dc.date.available2018-09-04T09:44:18Z-
dc.date.issued2014-01-01en_US
dc.identifier.issn18767486en_US
dc.identifier.issn18743900en_US
dc.identifier.other2-s2.0-84896311465en_US
dc.identifier.other10.1016/j.phytol.2014.02.004en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84896311465&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/53149-
dc.description.abstractThe genus Garcinia is a well known rich source of bioactive xanthones and benzophenones. Some species of this genus also produce flavonoids and biphenyls as minor constituents. In this study, two new biphenyls, doitungbiphenyls A (1) and B (2), along with two biphenyls, schomburgbiphenyl (3) and nigrolineabiphenyl B (4); and four xanthones, 1,3,6-trihydroxy-8-isoprenyl-7- methoxyxanthone (5), morusignin K (6), 1,5-dihydroxyxanthone (7), and 1,7-dihydroxyxanthone (8), were isolated from the acetone extract of the twigs of a Garcinia sp. Their structures were characterized extensively by 1D and 2D NMR spectroscopy and HR-EI-MS. The cytotoxicity of the two new biphenyls against the oral cavity cancer (KB) and the breast cancer (MCF7) cell lines was also evaluated. © 2014 Phytochemical Society of Europe.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleBiphenyl and xanthone derivatives from the twigs of a Garcinia sp. (Clusiaceae)en_US
dc.typeJournalen_US
article.title.sourcetitlePhytochemistry Lettersen_US
article.volume8en_US
article.stream.affiliationsMae Fah Luang Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Phayaoen_US
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