Publication:
Three non-phenolic diarylheptanoids with anti-inflammatory activity from Curcuma xanthorrhiza

dc.contributor.authorP. Claesonen_US
dc.contributor.authorA. Panthongen_US
dc.contributor.authorP. Tuchindaen_US
dc.contributor.authorV. Reutrakulen_US
dc.contributor.authorD. Kanjanapothien_US
dc.contributor.authorW. C. Tayloren_US
dc.contributor.authorT. Santisuken_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-08-10T08:53:56Z
dc.date.available2018-08-10T08:53:56Z
dc.date.issued1993-11-02en_US
dc.description.abstractBioassay-guided fractionation of a hexane extract of the rhizomes of Curcuma xanthorrhiza Roxb. (Zingiberaceae) led to the isolation of three non-phenolic diarylheptanoids, identified mainly by high-field 1H-NMR as trans-trans-1,7-diphenyl-1,3-heptadien-4-one (alnustone), trans-1,7-diphenyl-1-hepten-5-ol, and trans,trans-1,7-diphenyl-1,3-heptadien-5-ol. The latter is reported for the first time as a plant constituent. Germacrone, curzerenone, and cinnamaldehyde were also isolated and identified. The three diarylheptanoids all exerted significant anti-inflammatory activity in the assay of carrageenin-induced hind paw edema in rats.en_US
dc.identifier.citationPlanta Medica. Vol.59, No.5 (1993), 451-454en_US
dc.identifier.doi10.1055/s-2006-959730en_US
dc.identifier.issn00320943en_US
dc.identifier.other2-s2.0-0027519772en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/22511
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027519772&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleThree non-phenolic diarylheptanoids with anti-inflammatory activity from Curcuma xanthorrhizaen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0027519772&origin=inwarden_US

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