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dc.contributor.authorMoro, Antonio C.-
dc.contributor.authorMauro, Antonio Eduardo-
dc.contributor.authorNetto, Adelino Vieira de Godoy-
dc.contributor.authorAnanias, Sandra R.-
dc.contributor.authorQuilles, Marcela B.-
dc.contributor.authorCarlos, Iracilda Z.-
dc.contributor.authorPavan, Fernando R.-
dc.contributor.authorLeite, Clarice Q. F.-
dc.contributor.authorHoerner, Manfredo-
dc.date.accessioned2014-05-20T13:23:57Z-
dc.date.accessioned2016-10-25T16:44:48Z-
dc.date.available2014-05-20T13:23:57Z-
dc.date.available2016-10-25T16:44:48Z-
dc.date.issued2009-11-01-
dc.identifierhttp://dx.doi.org/10.1016/j.ejmech.2009.06.032-
dc.identifier.citationEuropean Journal of Medicinal Chemistry. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 44, n. 11, p. 4611-4615, 2009.-
dc.identifier.issn0223-5234-
dc.identifier.urihttp://hdl.handle.net/11449/7324-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/7324-
dc.description.abstractThe reactions between [Pd(C-2,N-dmba)(mu-X)](2) (dmba = N,N-dimethylbenzylamine: X = Cl, Br) and thiourea (tu) in the 1:2 molar ratio at room temperature resulted in the mononuclear compounds [Pd(C-2,N-dmba)(Cl)(tu)] (1) and [Pd(C-2,N-dmba)(Br)(tu)] (2), which were characterized by elemental analyses and infrared (IR), H-1- and C-13{H-1} NMR spectroscopies. The crystal and molecular structures of 2 were determined by single-crystal X-ray diffraction. In vitro cytotoxicity assays of the compounds 1, 2, tu, dmba and cisplatin were carried out using two murine tumor cell lines, namely mammary adenocarcinoma (LM3) and lung adenocarcinoma (LP07). The compounds 1, 2, tu and dmba were also tested against Mycobacterium tuberculosis and their MIC values were determined. (C) 2009 Elsevier Masson SAS. All rights reserved.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent4611-4615-
dc.language.isoeng-
dc.publisherElsevier France-editions Scientifiques Medicales Elsevier-
dc.sourceWeb of Science-
dc.subjectCyclopalladated complexen
dc.subjectCrystal structureen
dc.subjectcytotoxicity assaysen
dc.subjectMycobacterium tuberculosisen
dc.subjectAntitumoren
dc.subjectThioureaen
dc.titleAntitumor and antimycobacterial activities of cyclopalladated complexes: X-ray structure of [Pd(C-2,N-dmba)(Br)(tu)] (dmba = N,N-dimethylbenzylamine, tu = thiourea)en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade Federal de Santa Maria (UFSM)-
dc.description.affiliationUNESP, Inst Quim, Dept Quim Geral & Inorgan, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUNESP, Fac Ciencias Farmaceut, Dept Anal Clin, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUNESP, Fac Ciencias Farmaceut, Dept Ciencias Biol, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniversidade Federal de Santa Maria (UFSM), Ctr Ciencias Nat & Exatas, Dept Quim, BR-97105900 Santa Maria, RS, Brazil-
dc.description.affiliationUnespUNESP, Inst Quim, Dept Quim Geral & Inorgan, BR-14801970 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP, Fac Ciencias Farmaceut, Dept Anal Clin, BR-14801902 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP, Fac Ciencias Farmaceut, Dept Ciencias Biol, BR-14800900 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/j.ejmech.2009.06.032-
dc.identifier.wosWOS:000271225800041-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofEuropean Journal of Medicinal Chemistry-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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