Publicação: Phenolic Derivatives from Fruits of Dipteryx lacunifera DUCKE and Evaluation of Their Antiradical Activities
dc.contributor.author | Vieira Junior, Gerardo Magela [UNESP] | |
dc.contributor.author | Sotssa, Cleyton Marcos de A. | |
dc.contributor.author | Cavalheiro, Alberto José [UNESP] | |
dc.contributor.author | Lago, Joao Henrique G. | |
dc.contributor.author | Chaves, Mariana H. | |
dc.contributor.institution | Universidade Federal de São Paulo (UNIFESP) | |
dc.contributor.institution | Universidade Federal do Piauí (UFPI) | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.date.accessioned | 2014-05-20T14:20:56Z | |
dc.date.available | 2014-05-20T14:20:56Z | |
dc.date.issued | 2008-01-01 | |
dc.description.abstract | The 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.affiliation | Univ Fed São Paulo, Dept Ciencias Exatas & Terra, BR-09972270 Diadema, SP, Brazil | |
dc.description.affiliation | Univ Fed Piaui, Ctr Ciencias Nat, BR-05599970 Teresina, PI, Brazil | |
dc.description.affiliation | Univ Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil | |
dc.description.affiliationUnesp | Univ Estadual Paulista, Inst Quim, BR-14800900 Araraquara, SP, Brazil | |
dc.description.sponsorship | Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.format.extent | 2159-2167 | |
dc.identifier | http://dx.doi.org/10.1002/hlca.200890233 | |
dc.identifier.citation | Helvetica Chimica Acta. Weinheim: Wiley-v C H Verlag Gmbh, v. 91, n. 11, p. 2159-2167, 2008. | |
dc.identifier.doi | 10.1002/hlca.200890233 | |
dc.identifier.issn | 0018-019X | |
dc.identifier.lattes | 2518006820764120 | |
dc.identifier.uri | http://hdl.handle.net/11449/26277 | |
dc.identifier.wos | WOS:000261485200018 | |
dc.language.iso | eng | |
dc.publisher | Wiley-v C H Verlag Gmbh | |
dc.relation.ispartof | Helvetica Chimica Acta | |
dc.relation.ispartofjcr | 1.081 | |
dc.rights.accessRights | Acesso restrito | pt |
dc.source | Web of Science | |
dc.title | Phenolic Derivatives from Fruits of Dipteryx lacunifera DUCKE and Evaluation of Their Antiradical Activities | en |
dc.type | Artigo | pt |
dcterms.license | http://olabout.wiley.com/WileyCDA/Section/id-815640.html | |
dcterms.rightsHolder | Wiley-v C H Verlag Gmbh | |
dspace.entity.type | Publication | |
relation.isOrgUnitOfPublication | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
relation.isOrgUnitOfPublication.latestForDiscovery | bc74a1ce-4c4c-4dad-8378-83962d76c4fd | |
unesp.author.lattes | 2518006820764120[3] | |
unesp.author.orcid | 0000-0001-8214-9957[3] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Química, Araraquara | pt |
unesp.department | Química Orgânica - IQAR | pt |
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