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Phenolic Derivatives from Fruits of Dipteryx lacunifera DUCKE and Evaluation of Their Antiradical Activities

dc.contributor.authorVieira Junior, Gerardo Magela [UNESP]
dc.contributor.authorSotssa, Cleyton Marcos de A.
dc.contributor.authorCavalheiro, Alberto José [UNESP]
dc.contributor.authorLago, Joao Henrique G.
dc.contributor.authorChaves, Mariana H.
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniversidade Federal do Piauí (UFPI)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T14:20:56Z
dc.date.available2014-05-20T14:20:56Z
dc.date.issued2008-01-01
dc.description.abstractThe fruits of Dipteryx lacunifera, known as 'fava de morcego' and 'garampara', comprise pleasant tasting kernels that contain high amounts of fatty acids (mainly oleic acid) and are commonly consumed by inhabitants of the northeast of Brazil. In the present study, the crude EtOH extract of the fruit kernels was separated into hexane-, Et(2)O-, AcOEt-, and H(2)O-soluble fractions. The Et(2)O fraction was found to exhibit the highest 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical-scavenging activity in vitio, and was subjected to further fractionation. Column chromatography over silica gel and Sephadex LH-20, followed by preparative HPLC-C(18), afforded (-)-eriodictyol (1), (-)-butin (2), luteolin (3), 3',4',7- trihydroxyflavone(4), butein (5). and sulfuretin (6). The antiradical activities of compounds 1, 2, 4, and 6. together with the positive controls rutin,. butylated hydroxy toluene (BHT), and tert-butylhydroquinone (TBHQ), were evaluated with the DPPH assay and were found to decrease in the order rutin > 4 > 1 > 6 > 2 > TBHQ > BHT.en
dc.description.affiliationUniv Fed São Paulo, Dept Ciencias Exatas & Terra, BR-09972270 Diadema, SP, Brazil
dc.description.affiliationUniv Fed Piaui, Ctr Ciencias Nat, BR-05599970 Teresina, PI, Brazil
dc.description.affiliationUniv Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.format.extent2159-2167
dc.identifierhttp://dx.doi.org/10.1002/hlca.200890233
dc.identifier.citationHelvetica Chimica Acta. Weinheim: Wiley-v C H Verlag Gmbh, v. 91, n. 11, p. 2159-2167, 2008.
dc.identifier.doi10.1002/hlca.200890233
dc.identifier.issn0018-019X
dc.identifier.lattes2518006820764120
dc.identifier.urihttp://hdl.handle.net/11449/26277
dc.identifier.wosWOS:000261485200018
dc.language.isoeng
dc.publisherWiley-v C H Verlag Gmbh
dc.relation.ispartofHelvetica Chimica Acta
dc.relation.ispartofjcr1.081
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.titlePhenolic Derivatives from Fruits of Dipteryx lacunifera DUCKE and Evaluation of Their Antiradical Activitiesen
dc.typeArtigopt
dcterms.licensehttp://olabout.wiley.com/WileyCDA/Section/id-815640.html
dcterms.rightsHolderWiley-v C H Verlag Gmbh
dspace.entity.typePublication
relation.isOrgUnitOfPublicationbc74a1ce-4c4c-4dad-8378-83962d76c4fd
relation.isOrgUnitOfPublication.latestForDiscoverybc74a1ce-4c4c-4dad-8378-83962d76c4fd
unesp.author.lattes2518006820764120[3]
unesp.author.orcid0000-0001-8214-9957[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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