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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/26062
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dc.contributor.authorRegasini, Luis Octavio-
dc.contributor.authorCastro-Gamboa, Ian-
dc.contributor.authorSiqueira Silva, Dulce Helena-
dc.contributor.authorFurlan, Maysa-
dc.contributor.authorBarreiro, Eliezer Jesus-
dc.contributor.authorPinheiro Ferreira, Paulo Michel-
dc.contributor.authorPessoa, Claudia-
dc.contributor.authorCosta Lotufo, Leticia Veras-
dc.contributor.authorMoraes, Manoel Odorico de-
dc.contributor.authorMarx Young, Maria Claudia-
dc.contributor.authorBolzani, Vanderlan da Silva-
dc.date.accessioned2014-05-20T14:20:11Z-
dc.date.accessioned2016-10-25T17:41:29Z-
dc.date.available2014-05-20T14:20:11Z-
dc.date.available2016-10-25T17:41:29Z-
dc.date.issued2009-03-01-
dc.identifierhttp://dx.doi.org/10.1021/np800612x-
dc.identifier.citationJournal of Natural Products. Washington: Amer Chemical Soc, v. 72, n. 3, p. 473-476, 2009.-
dc.identifier.issn0163-3864-
dc.identifier.urihttp://hdl.handle.net/11449/26062-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/26062-
dc.description.abstractAs part of a bioprospecting program aimed at the discovery of potential anticancer drugs, two new guanidine-type alkaloids, nitensidines D and E (1, 2), and the known pterogynine (3), pterogynidine (4), and galegine (5), were isolated from the leaves of Pterogyne nitens. The structures of I and 2 were established on the basis of spectroscopic data interpretation. These compounds were tested against a small panel of human cancer cell lines. Compound 2 exhibited cytotoxicity for HL-60 (human myeloblastic leukemia) and SF-245 (human glioblastoma) cells.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.format.extent473-476-
dc.language.isoeng-
dc.publisherAmer Chemical Soc-
dc.sourceWeb of Science-
dc.titleCytotoxic Guanidine Alkaloids from Pterogyne nitensen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal do Rio de Janeiro (UFRJ)-
dc.contributor.institutionUniversidade Federal do Ceará (UFC)-
dc.contributor.institutionInst Bot-
dc.description.affiliationSão Paulo State Univ, Inst Chem, Nucley Bioassay Biosynth & Ecophys Nat Prod, UNESP, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUniv Fed Rio de Janeiro, LASSBio, Ctr Ciencias Saude, Fac Farm, BR-21944910 Rio de Janeiro, Brazil-
dc.description.affiliationUniversidade Federal do Ceará (UFC), LOE, Dept Fisiol & Farmacol, BR-60430270 Fortaleza, Ceara, Brazil-
dc.description.affiliationInst Bot, BR-01061970 São Paulo, Brazil-
dc.description.affiliationUnespSão Paulo State Univ, Inst Chem, Nucley Bioassay Biosynth & Ecophys Nat Prod, UNESP, BR-14801970 Araraquara, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 03/02176-7-
dc.identifier.doi10.1021/np800612x-
dc.identifier.wosWOS:000264627600025-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Natural Products-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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