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dc.contributor.authorFlausino, Otavio-
dc.contributor.authorSantos, Luciana de Avila-
dc.contributor.authorVerli, Hugo-
dc.contributor.authorPereira, Ana Maria-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.contributor.authorNunes-de-Souza, Ricardo Luiz-
dc.date.accessioned2014-05-20T15:23:14Z-
dc.date.accessioned2016-10-25T17:57:08Z-
dc.date.available2014-05-20T15:23:14Z-
dc.date.available2016-10-25T17:57:08Z-
dc.date.issued2007-01-01-
dc.identifierhttp://dx.doi.org/10.1021/np060254j-
dc.identifier.citationJournal of Natural Products. Washington: Amer Chemical Soc, v. 70, n. 1, p. 48-53, 2007.-
dc.identifier.issn0163-3864-
dc.identifier.urihttp://hdl.handle.net/11449/34065-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/34065-
dc.description.abstractOne new erythrinian alkaloid derivative, (+)-11 alpha-hydroxyerythravine (1), and the known (+)-erythravine (2) and (+)-alpha-hydroxyerysotrine (3) were isolated from the flowers of Erythrina mulungu. Their structures were determined by spectroscopic/spectrometric data interpretation of H-1, C-13, and 2D NMR and MS experiments. The relative configuration was established by NOESY analysis, while the conformation adopted by these molecules was evaluated through molecular modeling studies and coupling constants obtained by NMR analysis. Furthermore, the anxiolytic effects of the E. mulungu aqueous alcoholic crude extract and of the purified alkaloids were evaluated using the elevated T-maze test.en
dc.format.extent48-53-
dc.language.isoeng-
dc.publisherAmer Chemical Soc-
dc.sourceWeb of Science-
dc.titleAnxiolytic effects of erythrinian alkaloids from Erythrina mulunguen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniv Ribeirao Preto-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.contributor.institutionUniversidade Federal do Rio Grande do Sul (UFRGS)-
dc.description.affiliationSão Paulo State Univ, Inst Chem, NuBBE, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniv Ribeirao Preto, Dept Vegetal Biotechnol, BR-14096380 Ribeirao Preto, Brazil-
dc.description.affiliationUniv São Paulo, FFCLRP, Dept Psychobiol, BR-14040901 Ribeirao Preto, Brazil-
dc.description.affiliationSão Paulo State Univ, Pharmacol Lab, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUniv Fed Rio Grande Sul, Fac Pharm, BR-90610000 Porto Alegre, RS, Brazil-
dc.description.affiliationUniv Fed Rio Grande Sul, Ctr Biotechnol, BR-91500970 Porto Alegre, RS, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Inst Chem, NuBBE, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Pharmacol Lab, BR-14801902 Araraquara, SP, Brazil-
dc.identifier.doi10.1021/np060254j-
dc.identifier.wosWOS:000243734900011-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Natural Products-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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