Publication:
Diterpenoids from the roots of Croton oblongifolius

dc.contributor.authorWitoon Youngsa-aden_US
dc.contributor.authorNattaya Ngamrojanavanichen_US
dc.contributor.authorChulabhorn Mahidolen_US
dc.contributor.authorSomsak Ruchirawaten_US
dc.contributor.authorHunsa Prawaten_US
dc.contributor.authorPrasat Kittakoopen_US
dc.contributor.otherChulabhorn Research Instituteen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherChulabhorn Graduate Instituteen_US
dc.contributor.otherThe Institute of Science and Technology for Research and Development, Mahidol Universityen_US
dc.date.accessioned2018-08-24T01:36:58Z
dc.date.available2018-08-24T01:36:58Z
dc.date.issued2007-11-01en_US
dc.description.abstractTwo new clerodane diterpenes, methyl 15,16-epoxy-3,13(16),14-ent- clerodatrien-18,19-olide-17-carboxylate (1) and dimethyl 15,16-epoxy-12-oxo-3, 13(16),14-ent-clerodatriene-17,18-dicarboxylate (2), together with seven known compounds (3-9), were isolated from the roots of Croton oblongifolius. The isolated compounds showed only mild cytotoxic activity against HuCCA-1, KB, HeLa, MDA-MB231, and T47D cell lines with IC50 values ranging from 10 to 50 μg/mL. © Georg Thieme Verlag KG Stuttgart.en_US
dc.identifier.citationPlanta Medica. Vol.73, No.14 (2007), 1491-1494en_US
dc.identifier.doi10.1055/s-2007-990247en_US
dc.identifier.issn00320943en_US
dc.identifier.other2-s2.0-36949003723en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/23969
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=36949003723&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleDiterpenoids from the roots of Croton oblongifoliusen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=36949003723&origin=inwarden_US

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