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.authorDe Almeida, K. J.
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.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-29T07:26:06Z
dc.date.available2022-04-29T07:26:06Z
dc.date.issued2015-07-02
dc.description.abstractThis work reports on the synthesis and characterization of complexes of the type cis-[Pt(L)<inf>2</inf>X<inf>2</inf>], 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<sup>-</sup> or I<sup>-</sup>. 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 NH<inf>2</inf> 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.en
dc.description.affiliationInstituto de Química, Universidade Federal de Uberlândia, Campus Santa Mônica, Av. João Naves de Ávila, 2121
dc.description.affiliationDepartamento de Química, Universidade Federal de Minas Gerais, Campus Pampulha
dc.description.affiliationDepartamento de Química, Universidade Federal de São Carlos
dc.description.affiliationDepartamento de Química, Universidade Federal de Juiz de Fora
dc.description.affiliationDepartamento de Ciências Biológicas, Universidade Estadual Paulista, Campus Araraquara
dc.description.affiliationDepartamento de Química, Universidade de Federal de Lavras
dc.description.affiliationUnespDepartamento de Ciências Biológicas, Universidade Estadual Paulista, Campus Araraquara
dc.format.extent146-153
dc.identifierhttp://dx.doi.org/10.1016/j.poly.2015.06.025
dc.identifier.citationPolyhedron, v. 98, p. 146-153.
dc.identifier.doi10.1016/j.poly.2015.06.025
dc.identifier.issn0277-5387
dc.identifier.scopus2-s2.0-84933520888
dc.identifier.urihttp://hdl.handle.net/11449/228000
dc.language.isoeng
dc.relation.ispartofPolyhedron
dc.sourceScopus
dc.subjectCarbazate
dc.subjectComputational modeling
dc.subjectCytotoxic activity
dc.subjectHydrazide
dc.subjectPlatinum complexes
dc.titlePlatinum(II) complexes with carbazates and hydrazides: Synthesis, spectral characterization, computational modeling, and biological studiesen
dc.typeArtigo
unesp.departmentCiências Biológicas - FCFpt

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