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Cytotoxic lignans from the stems of Styrax camporum (Styracaceae)

dc.contributor.authorTeles, Helder L. [UNESP]
dc.contributor.authorHemerly, J. P.
dc.contributor.authorPauletti, Patrícia M. [UNESP]
dc.contributor.authorPandolfi, José R. C. [UNESP]
dc.contributor.authorAraujo, Angela Regina [UNESP]
dc.contributor.authorValentini, Sandro Roberto [UNESP]
dc.contributor.authorYoung, M. Cláudia M.
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.contributor.authorSilva, Dulce H. S. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionInst Bot
dc.date.accessioned2014-05-20T13:24:32Z
dc.date.available2014-05-20T13:24:32Z
dc.date.issued2005-06-01
dc.description.abstractAn ethanolic extract from the stems of Styrax camporum Pohl (Styracaceae), a plant traditionally used for gastrointestinal diseases, was fractionated and subjected to flash chromatography and afforded two benzofuran lignans, egonol and homoegonol, and one furofuran lignan, (+/-) syringaresinol, which were identified by spectral data interpretation. Their cytotoxic activities against Hep-2 (larynx epidermoid carcinoma), HeLa (human cervix carcinoma) and C6 (rat glioma) cell lines were evaluated using the MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide) assay at several concentrations for 24 h. Activities could be observed for egonol against C6 (IC50 = 3.2 mu g/mL) and Hep-2 (IC50 = 3.6 mu g/mL) cell lines, and for homoegonol against C6 (IC50 = 4.9 mu g/mL) and HeLa (IC50 =- 5.3 mu g/mL) cells.en
dc.description.affiliationUNESP, Inst Quim, BR-14800900 Araraquara, Brazil
dc.description.affiliationUNIFESP, Escola Paulista Med, BR-14801902 Araraquara, Brazil
dc.description.affiliationUNESP, Fac Ciências Farmaceut, BR-14801902 Araraquara, Brazil
dc.description.affiliationInst Bot, Secao Fisiol & Bioquim Plantas, BR-01061970 São Paulo, Brazil
dc.description.affiliationUnespUNESP, Inst Quim, BR-14800900 Araraquara, Brazil
dc.description.affiliationUnespUNESP, Fac Ciências Farmaceut, BR-14801902 Araraquara, Brazil
dc.format.extent319-323
dc.identifierhttp://dx.doi.org/10.1080/14786410412331271979
dc.identifier.citationNatural Product Research. Abingdon: Taylor & Francis Ltd, v. 19, n. 4, p. 319-323, 2005.
dc.identifier.doi10.1080/14786410412331271979
dc.identifier.issn1478-6419
dc.identifier.lattes0037579054083160
dc.identifier.lattes4484083685251673
dc.identifier.lattes4702004904231248
dc.identifier.orcid0000-0001-7616-9652
dc.identifier.orcid0000-0002-1516-7765
dc.identifier.urihttp://hdl.handle.net/11449/7649
dc.identifier.wosWOS:000229394900003
dc.language.isoeng
dc.publisherTaylor & Francis Ltd
dc.relation.ispartofNatural Product Research
dc.relation.ispartofjcr1.928
dc.relation.ispartofsjr0,671
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectStyrax camporumpt
dc.subjectStyracaceaept
dc.subjectcytotoxic lignanspt
dc.subjectMTT assaypt
dc.titleCytotoxic lignans from the stems of Styrax camporum (Styracaceae)en
dc.typeArtigopt
dcterms.licensehttp://journalauthors.tandf.co.uk/permissions/reusingOwnWork.asp
dcterms.rightsHolderTaylor & Francis Ltd
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes0037579054083160[5]
unesp.author.lattes4484083685251673
unesp.author.lattes4702004904231248[9]
unesp.author.orcid0000-0001-7616-9652[5]
unesp.author.orcid0000-0002-1516-7765[9]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentQuímica Orgânica - IQARpt

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