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dc.contributor.authorViegas, Cláudio
dc.contributor.authorPivatto, Marcos
dc.contributor.authorDe Rezende, Amanda [UNESP]
dc.contributor.authorHamerski, Lidilhone [UNESP]
dc.contributor.authorSilva, Dulce Helena Siqueira [UNESP]
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.date.accessioned2014-05-27T11:28:50Z
dc.date.available2014-05-27T11:28:50Z
dc.date.issued2013-04-02
dc.identifierhttp://dx.doi.org/10.5935/0103-5053.20130029
dc.identifier.citationJournal of the Brazilian Chemical Society, v. 24, n. 2, p. 230-235, 2013.
dc.identifier.issn0103-5053
dc.identifier.issn1678-4790
dc.identifier.urihttp://hdl.handle.net/11449/75053
dc.description.abstractThe phytochemical study of flowers and green fruits of Senna spectabilis furnished a new substituted 2,6-dialkylpiperidin-3-ol alkaloid, named (-)-7-hydroxycassine, along with five known piperidine alkaloids: (-)-cassine, (-)-spectaline, (-)-3-O-acetylspectaline, (-)-7-hydroxyspectaline and (-)-iso-6-spectaline. In addition to non-alkaloidal, chemical constituents from other chemical classes were also identified, including the steroid β-sitosterol, the flavonoids luteolin and 3-methoxyluteolin, the triterpene betulinic acid and trans-cinnamic acid. To our knowledge, compounds are being reported for the first time in this species. © 2013 Sociedade Brasileira de Quimica.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.format.extent230-235
dc.language.isoeng
dc.relation.ispartofJournal of the Brazilian Chemical Society
dc.sourceScopus
dc.subject(-)-7-hydroxycassine
dc.subjectPiperidine alkaloids
dc.subjectSenna spectabilis
dc.title7-Hydroxycassine: A new 2,6-dialkylpiperidin-3-ol alkaloid and other constituents isolated from flowers and fruits of senna spectabilis (Fabaceae)en
dc.typeArtigo
dcterms.licensehttp://jbcs.sbq.org.br/copyright
dc.contributor.institutionFederal University of Alfenas
dc.contributor.institutionFederal University of Uberlâdia
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.description.affiliationPhytochemistry and Medicinal Chemistry Laboratory (LFQM) Institute of Chemistry Federal University of Alfenas, 37130-000 Alfenas-MG
dc.description.affiliationInstitute of Chemistry Federal University of Uberlâdia, 38400-902 Uberlǎndia-MG
dc.description.affiliationOrganic Chemistry Department Institute of Chemistry São Paulo State University (UNESP) 'Júlio de Mesquita Filho', CP 355, 14801-970 Araraquara-SP
dc.description.affiliationUnespOrganic Chemistry Department Institute of Chemistry São Paulo State University (UNESP) 'Júlio de Mesquita Filho', CP 355, 14801-970 Araraquara-SP
dc.identifier.doi10.5935/0103-5053.20130029
dc.identifier.wosWOS:000317922100008
dc.rights.accessRightsAcesso aberto
dc.description.sponsorshipIdFAPESP: 03/02176-7
dc.identifier.scopus2-s2.0-84875416923
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
dc.identifier.file2-s2.0-84875416923.pdf
dc.identifier.lattes4702004904231248
dc.identifier.lattes4484083685251673
dc.identifier.orcid0000-0002-1516-7765
unesp.author.lattes4702004904231248[5]
unesp.author.lattes4484083685251673
unesp.author.orcid0000-0002-1516-7765[5]
dc.relation.ispartofjcr1.444
dc.relation.ispartofsjr0,357
dc.relation.ispartofsjr0,357
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