dc.contributorUniversidade Estadual Paulista (Unesp)
dc.contributorUniversidade Federal do Piauí (UFPI)
dc.contributorUniversidade Federal do Ceará (UFC)
dc.date.accessioned2014-05-20T14:20:15Z
dc.date.accessioned2022-10-05T15:20:06Z
dc.date.available2014-05-20T14:20:15Z
dc.date.available2022-10-05T15:20:06Z
dc.date.created2014-05-20T14:20:15Z
dc.date.issued2010-01-01
dc.identifierChemistry & Biodiversity. Weinheim: Wiley-v C H Verlag Gmbh, v. 7, n. 1, p. 205-215, 2010.
dc.identifier1612-1872
dc.identifier1612-1880
dc.identifierhttp://hdl.handle.net/11449/26084
dc.identifier10.1002/cbdv.200800342
dc.identifierWOS:000274264000014
dc.identifier2-s2.0-75449106161
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3899119
dc.description.abstractAn EtOH extract of the leaves of Casearia sylvestris afforded new clerodane diterpene, casearin X, together with the known compounds casearins B, D, L, and O, and caseargrewiin F Casearin X degraded to the corresponding dialdehyde when stored in CDCl(3). The diterpenes isolated were cytotoxic to human cancer cell lines, with caseargrewiin F being the most active and the new clerodane, casearin X, the second active compound with IC(50) values comparable to the positive control doxorubicin. All isolated diterpenes showed lower activities against normal human cells than against cancer cell lines, which might indicate a possible selective action on cancer cells. Casearin X dialdehyde was not cytotoxic to cancer cells indicating that the occurrence of these CO groups at C(18) and C(19) is incompatible with the cytotoxic activity.
dc.languageeng
dc.publisherWiley-v C H Verlag Gmbh
dc.relationChemistry & Biodiversity
dc.relation1.617
dc.relation0,531
dc.relation0,531
dc.rightsAcesso restrito
dc.sourceWeb of Science
dc.titleCasearin X, Its Degradation Product and Other Clerodane Diterpenes from Leaves of Casearia sylvestris: Evaluation of Cytotoxicity against Normal and Tumor Human Cells
dc.typeArtigo


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