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Alkaloids from Stems of Esenbeckia leiocarpa Engl. (Rutaceae) as Potential Treatment for Alzheimer Disease

dc.contributor.authorCardoso-Lopes, Elaine Monteiro
dc.contributor.authorMaier, James Andreas
dc.contributor.authorda Silva, Marcelo Rogerio
dc.contributor.authorRagasini, Luis Octavio [UNESP]
dc.contributor.authorSimote, Simone Yasue [UNESP]
dc.contributor.authorLopes, Norberto Peporine
dc.contributor.authorPirani, Jose Rubens
dc.contributor.authorBolzani, Vanderlan da Silva [UNESP]
dc.contributor.authorMarx Young, Maria Claudia
dc.contributor.institutionInst Bot
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T14:20:32Z
dc.date.available2014-05-20T14:20:32Z
dc.date.issued2010-12-01
dc.description.abstractEsenbeckia leiocarpa Engl. (Rutaceae), popularly known as guaranta, goiabeira, is a native tree from Brazil. Bioactivity-guided fractionation of the ethanol stems extract afforded the isolation of six alkaloids: leiokinine A, leptomerine, kokusaginine, skimmianine, maculine and flindersiamine. All isolated compounds were tested for acetyl cholinesterase inhibition, in vitro and displayed anticholinesterasic activity. The alkaloid leptomerine showed the highest activity (IC(50) = 2.5 mu M), similar to that of the reference compound galanthamine (IC(50) = 1.7 mu M). The results showed for the first time the presence of alkaloids leptomerine and skimmianine in E. leiocarpa (Engl.) with potent anticholinesterasic activity.en
dc.description.affiliationInst Bot, Sect Plant Physiol & Biochem, BR-01061970 São Paulo, Brazil
dc.description.affiliationSão Paulo State Univ, Inst Chem, BR-14801970 Araraquara, SP, Brazil
dc.description.affiliationUniv São Paulo, Dept Chem & Phys, BR-14040903 Ribeirao Preto, SP, Brazil
dc.description.affiliationUniv São Paulo, Dept Bot, Biosci Inst, BR-05422970 São Paulo, Brazil
dc.description.affiliationUnespSão Paulo State Univ, Inst Chem, BR-14801970 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.description.sponsorshipIdFAPESP: 03/02176-7
dc.format.extent9205-9213
dc.identifierhttp://dx.doi.org/10.3390/molecules15129205
dc.identifier.citationMolecules. Basel: Mdpi Ag, v. 15, n. 12, p. 9205-9213, 2010.
dc.identifier.doi10.3390/molecules15129205
dc.identifier.fileWOS000285709000045.pdf
dc.identifier.issn1420-3049
dc.identifier.lattes4484083685251673
dc.identifier.urihttp://hdl.handle.net/11449/26167
dc.identifier.wosWOS:000285709000045
dc.language.isoeng
dc.publisherMdpi Ag
dc.relation.ispartofMolecules
dc.relation.ispartofjcr3.098
dc.relation.ispartofsjr0,855
dc.rights.accessRightsAcesso aberto
dc.sourceWeb of Science
dc.subjectEsenbeckia leiocarpaen
dc.subjectRutaceaeen
dc.subjectalkaloidsen
dc.subjectacetylcholinesterase inhibitorsen
dc.titleAlkaloids from Stems of Esenbeckia leiocarpa Engl. (Rutaceae) as Potential Treatment for Alzheimer Diseaseen
dc.typeArtigo
dcterms.licensehttp://www.mdpi.com/about/openaccess
dcterms.rightsHolderMdpi Ag
dspace.entity.typePublication
unesp.author.lattes4484083685251673
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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