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Platinum(II) complexes with carbazates and hydrazides: Synthesis, spectral characterization, computational modeling, and biological studies

dc.contributor.authorRodrigues, M. A.
dc.contributor.authorMarzano, I. M.
dc.contributor.authorRibeiro, G. H.
dc.contributor.authorColina-Vegas, L.
dc.contributor.authorPivatto, M.
dc.contributor.authorFontes, A. P. S.
dc.contributor.authorRibeiro, C. M. [UNESP]
dc.contributor.authorPavan, F. R. [UNESP]
dc.contributor.authorAlmeida, K. J. de
dc.contributor.authorBatista, A. A.
dc.contributor.authorPereira-Maia, E. C.
dc.contributor.authorGuerra, W.
dc.contributor.institutionUniversidade Federal de Uberlândia (UFU)
dc.contributor.institutionUniversidade Federal de Minas Gerais (UFMG)
dc.contributor.institutionUniversidade Federal de São Carlos (UFSCar)
dc.contributor.institutionUniv Fed Juiz de Fora
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal de Lavras (UFLA)
dc.date.accessioned2018-11-26T16:17:05Z
dc.date.available2018-11-26T16:17:05Z
dc.date.issued2015-09-25
dc.description.abstractThis work reports on the synthesis and characterization of complexes of the type cis-[Pt(L)(2)X-2], where L = 4-methoxybenzylcarbazate (4-MC), benzyl carbazate (BC), 4-fluorophenoxyacetic acid hydrazide (4-FH), 3-methoxybenzoic acid hydrazide (3-MH), ethyl carbazate (EC), tert-butyl carbazate (TC), (4-hydroxy-phenyl)-acetic acid hydrazide (4-HH), and X = Cl- or l(-). The structures of the platinum(II) complexes were optimized and theoretical data show good agreement with the experimental results, suggesting that the ligands are coordinated via the NH2 groups. The cytotoxic activity of three representative compounds was evaluated in a chronic myelogenous leukemia cell line and health cell line from mouse (L929). The platinum complex with 4-fluorophenoxyacetic acid hydrazide was more active than the free ligand and carboplatin therefore it may be considered a promising antitumor agent. In addition, the platinum complexes with 4-methoxybenzylcarbazate (4-MC) and benzyl carbazate (BC) exhibited good activity. On the other hand, microbiological assays against Mycobacterium tuberculosis showed that all complexes and organic compounds are not very active. (C) 2015 Elsevier Ltd. All rights reserved.en
dc.description.affiliationUniv Fed Uberlandia, Inst Quim, BR-38400902 Uberlandia, MG, Brazil
dc.description.affiliationUniv Fed Minas Gerais, Dept Quim, BR-31270901 Belo Horizonte, MG, Brazil
dc.description.affiliationUniv Fed Sao Carlos, Dept Quim, BR-13565905 Sao Carlos, SP, Brazil
dc.description.affiliationUniv Fed Juiz de Fora, Dept Quim, BR-36036900 Juiz De Fora, MG, Brazil
dc.description.affiliationUniv Estadual Paulista, Dept Ciencias Biol, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUniv Fed Lavras, Dept Quim, BR-37200000 Lavras, MG, Brazil
dc.description.affiliationUnespUniv Estadual Paulista, Dept Ciencias Biol, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipRMQ (Rede Mineira de Quimica, Brazil)
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG)
dc.description.sponsorshipINCT-Catalise
dc.description.sponsorshipIdFAPEMIG: APQ-00330-14
dc.format.extent146-153
dc.identifier.citationPolyhedron. Oxford: Pergamon-elsevier Science Ltd, v. 98, p. 146-153, 2015.
dc.identifier.fileWOS000362143900020.pdf
dc.identifier.issn0277-5387
dc.identifier.urihttp://hdl.handle.net/11449/160874
dc.identifier.wosWOS:000362143900020
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofPolyhedron
dc.relation.ispartofsjr0,472
dc.rights.accessRightsAcesso abertopt
dc.sourceWeb of Science
dc.subjectPlatinum complexes
dc.subjectHydrazide
dc.subjectCarbazate
dc.subjectComputational modeling
dc.subjectCytotoxic activity
dc.titlePlatinum(II) complexes with carbazates and hydrazides: Synthesis, spectral characterization, computational modeling, and biological studiesen
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
unesp.departmentCiências Biológicas - FCFpt

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