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Utilize este identificador para citar ou criar um link para este item: http://acervodigital.unesp.br/handle/11449/17530
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dc.contributor.authorSeito, Leonardo Noboru-
dc.contributor.authorTasca Goiz Ruiz, Ana Lucia-
dc.contributor.authorVendramini-Costa, Debora-
dc.contributor.authorTinti, Sirlene Valerio-
dc.contributor.authorde Carvalho, Joao Ernesto-
dc.contributor.authorBastos, Jairo Kenupp-
dc.contributor.authorDi Stasi, Luiz Claudio-
dc.date.accessioned2014-05-20T13:49:14Z-
dc.date.accessioned2016-10-25T17:01:46Z-
dc.date.available2014-05-20T13:49:14Z-
dc.date.available2016-10-25T17:01:46Z-
dc.date.issued2011-10-01-
dc.identifierhttp://dx.doi.org/10.1002/ptr.3438-
dc.identifier.citationPhytotherapy Research. Malden: Wiley-blackwell, v. 25, n. 10, p. 1447-1450, 2011.-
dc.identifier.issn0951-418X-
dc.identifier.urihttp://hdl.handle.net/11449/17530-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/17530-
dc.description.abstractThe present study isolated three major active flavonoids, two flavones named 4',5,7-trimethoxy-luteolin (1) and 6-hydroxy-5,7-dimethoxyflavone (2) and the flavanone 5-hydroxy-6,7-dimethoxyflavanone (3) from Zeyheria montana dichloromethane leaf extract. Isolation and purification were conducted with the application of column chromatography and structures were assigned by spectral analysis. All compounds were evaluated for cytotoxic activities against human tumor cell lines UACC-62 (melanoma), MCF-7 (breast), NCI-ADR/RES (breast expressing phenotype multiple drug resistance), 786-0 (renal), NCI-H460 (lung, non-small cells), PC-3 (prostate), OVCAR-3 (ovarian), HT-29 (colon) and K562 (leukemia) in vitro. All compounds were active in different degrees on several tumor cell lines and flavanone 3 showed cytotoxicity against almost all cell lines, particularly against human NCI-ADR/RES and K562 cell lines. In conclusion, three antiproliferative compounds were isolated for the first time from Zeyheria montana and its leaves were characterized as an important source of methoxylated flavones and flavanone as potential antitumor compounds. Copyright (C) 2011 John Wiley & Sons, Ltd.en
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.format.extent1447-1450-
dc.language.isoeng-
dc.publisherWiley-Blackwell-
dc.sourceWeb of Science-
dc.subjectZeyheria Montanaen
dc.subjectBignoniaceaeen
dc.subjectflavonoidsen
dc.subjectantiproliferative activityen
dc.subjectflavonesen
dc.subjectflavanonesen
dc.titleAntiproliferative Activity of Three Methoxylated Flavonoids Isolated from Zeyheria montana Mart. (Bignoniaceae) Leavesen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUniv Estadual Paulista UNESP, Lab Phytomed, Dept Pharmacol, Inst Biociencias, BR-18618000 Botucatu, SP, Brazil-
dc.description.affiliationUniv Estadual Campinas, Ctr Pluridisciplinar Pesquisas Quim Biol & Agr, UNICAMP, BR-13083970 Campinas, SP, Brazil-
dc.description.affiliationUniv São Paulo, Lab Farmacognosia, Fac Ciencias Farmaceut Ribeirao Preto, BR-14040903 Ribeirao Preto, SP, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista UNESP, Lab Phytomed, Dept Pharmacol, Inst Biociencias, BR-18618000 Botucatu, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 03/09324-1-
dc.description.sponsorshipIdCNPq: 399176/2006-09-
dc.identifier.doi10.1002/ptr.3438-
dc.identifier.wosWOS:000295962500005-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofPhytotherapy Research-
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