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Prenylated flavanones from Derris reticulata

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dc.contributor.authorChulabhorn Mahidolen_US
dc.contributor.authorHunsa Prawaten_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.authorKittisak Lihkitwitayawuiden_US
dc.contributor.authorLong Ze Linen_US
dc.contributor.authorGeoffrey A. Cordellen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUniversity of Illinois at Chicagoen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.date.accessioned2018-07-04T07:39:24Z
dc.date.available2018-07-04T07:39:24Z
dc.date.issued1997-06-01en_US
dc.description.abstractTwo new pyranoflavanones, 2''',3'''-epoxylupinifolin and dereticulatin, together with the known flavonoid lupinifolin, were identified from the stems of Derris reticulata. The structures and NMR spectral data were assigned by the use of 2D NMR technology and chemical transformations. All of the isolates showed cytotoxic activity in the P-388 cell line.en_US
dc.identifier.citationPhytochemistry. Vol.45, No.4 (1997), 825-829en_US
dc.identifier.doi10.1016/S0031-9422(97)00001-0en_US
dc.identifier.issn00319422en_US
dc.identifier.other2-s2.0-0030926132en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/17860
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0030926132&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titlePrenylated flavanones from Derris reticulataen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0030926132&origin=inwarden_US

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