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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/7462
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dc.contributor.authorde Souza, Rodrigo A.-
dc.contributor.authorStevanato, Alessandra-
dc.contributor.authorTreu-Filho, Oswaldo-
dc.contributor.authorNetto, Adelino Vieira de Godoy-
dc.contributor.authorMauro, Antonio Eduardo-
dc.contributor.authorCastellano, Eduardo E.-
dc.contributor.authorCarlos, Iracilda Z.-
dc.contributor.authorPavan, Fernando R.-
dc.contributor.authorLeite, Clarice Q. F.-
dc.date.accessioned2014-05-20T13:24:14Z-
dc.date.accessioned2016-10-25T16:44:58Z-
dc.date.available2014-05-20T13:24:14Z-
dc.date.available2016-10-25T16:44:58Z-
dc.date.issued2010-11-01-
dc.identifierhttp://dx.doi.org/10.1016/j.ejmech.2010.07.057-
dc.identifier.citationEuropean Journal of Medicinal Chemistry. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 45, n. 11, p. 4863-4868, 2010.-
dc.identifier.issn0223-5234-
dc.identifier.urihttp://hdl.handle.net/11449/7462-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/7462-
dc.description.abstractComplexes of the type trans-[PdX2(isn)(2)] {X = Cl (1), N-3 (2), SCN (3), NCO (4); isn = isonicotinamide} were synthesized and evaluated for in vitro antimycobacterial and antitumor activities. The coordination mode of the isonicotinamide and the pseudohalide ligands was inferred by IR spectroscopy. Single crystal X-ray diffraction determination on 2 showed that coordination geometry around Pd(II) is nearly square planar, with the ligands in a trans configuration. All the compounds demonstrated better in vitro activity against Mycobacterium tuberculosis than isonicotinamide and pyrazinamide. Among the complexes, compound 2 was found to be the most active with MIC of 35.89 mu M. Complexes 1-4 were also screened for their in vitro antitumor activity towards LM3 and LP07 murine cancer cell lines. (C) 2010 Elsevier Masson SAS. All rights reserved.en
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent4863-4868-
dc.language.isoeng-
dc.publisherElsevier France-editions Scientifiques Medicales Elsevier-
dc.sourceWeb of Science-
dc.subjectPalladium(II) complexesen
dc.subjectIsonicotinamideen
dc.subjectCytotoxicity assaysen
dc.subjectAntimycobacterialen
dc.subjectAntitumor activityen
dc.titleAntimycobacterial and antitumor activities of Palladium(II) complexes containing isonicotinamide (isn): X-ray structure of trans-[Pd(N-3)(2)(isn)(2)]en
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUNESP São Paulo State Univ, Inst Quim Araraquara, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUniv São Paulo, Inst Fis São Carlos, BR-13560970 São Carlos, SP, Brazil-
dc.description.affiliationUNESP São Paulo State Univ, Fac Ciencias Farmaceut, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Inst Quim Araraquara, BR-14800900 Araraquara, SP, Brazil-
dc.description.affiliationUnespUNESP São Paulo State Univ, Fac Ciencias Farmaceut, BR-14800900 Araraquara, SP, Brazil-
dc.identifier.doi10.1016/j.ejmech.2010.07.057-
dc.identifier.wosWOS:000283911300020-
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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