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dc.contributor.authorAlmeida, Carolane de Macêdo-
dc.contributor.authorNascimento, Érica Cristina Moreno-
dc.contributor.authorMartins, João Batista Lopes-
dc.contributor.authorMota, Tales Henrique Andrade da-
dc.contributor.authorOliveira, Diêgo Madureira de-
dc.contributor.authorGatto, Claudia Cristina-
dc.date.accessioned2024-07-15T15:38:55Z-
dc.date.available2024-07-15T15:38:55Z-
dc.date.issued2023-07-14-
dc.identifier.citationALMEIDA, Carolane M. et al. Crystal design, antitumor activity and molecular docking of novel Palladium(II) and Gold(III) complexes with a Thiosemicarbazone ligand. International Journal of Molecular Sciences, [S. l.], v. 24, n. 14, 11442, 2023.pt_BR
dc.identifier.urihttp://repositorio.unb.br/handle/10482/48852-
dc.language.isoengpt_BR
dc.publisherMDPIpt_BR
dc.rightsAcesso Abertopt_BR
dc.titleCrystal design, antitumor activity and molecular docking of novel Palladium(II) and Gold(III) complexes with a Thiosemicarbazone ligandpt_BR
dc.typeArtigopt_BR
dc.subject.keywordComplexos metálicospt_BR
dc.subject.keywordAtividade antitumoralpt_BR
dc.subject.keywordTiossemicarbazonapt_BR
dc.subject.keywordSuperfície de Hirshfeldpt_BR
dc.subject.keywordDocking molecularpt_BR
dc.rights.license© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).-
dc.description.abstract1The current research describes the synthesis and characterization of 2-acetylpyridine N(4)-cyclohexyl-thiosemicarbazone ligand (HL) and their two metal complexes, [Au(L)Cl][AuCl2] (1) and [Pd(L)Cl]·DMF (2). The molecular structures of the compounds were determined by physicochemical and spectroscopic methods. Single crystal X-ray diffraction was employed in the structural elucidation of the new complexes. The complexes showed a square planar geometry to the metal center Au(III) and Pd(II), coordinated with a thiosemicarbazone molecule by the NNS-donor system and a chloride ion. Complex (1) also shows the [AuCl2 ] − counter-ion in the asymmetric unit, and complex (2) has one DMF solvent molecule. These molecules play a key role in the formation of supramolecular structures due to different interactions. Noncovalent interactions were investigated through the 3D Hirshfeld surface by the dnorm function and the 2D fingerprint plots. The biological activity of the compounds was evaluated in vitro against the human glioma U251 cells. The cytotoxicity results revealed great antitumor activity in complex (1) compared with complex (2) and the free ligand. Molecular docking simulations were used to predict interactions and properties with selected proteins and DNA of the synthesized compounds.pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-8677-3239pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0001-9299-9410pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-6044-1954pt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-3736-6861pt_BR
dc.contributor.affiliationUniversity of Brasilia, Institute of Chemistry, Laboratory of Inorganic Synthesis and Crystallographypt_BR
dc.contributor.affiliationUniversity of Brasilia, Institute of Chemistry, Laboratory of Computational Chemistrypt_BR
dc.contributor.affiliationUniversity of Brasilia, Institute of Chemistry, Laboratory of Computational Chemistrypt_BR
dc.contributor.affiliationUniversity of Brasilia, Faculty UnB Ceilândia, Multidisciplinary Laboratory of Human Healthpt_BR
dc.contributor.affiliationUniversity of Brasilia, Faculty UnB Ceilândia, Multidisciplinary Laboratory of Human Healthpt_BR
dc.contributor.affiliationUniversity of Brasilia, Institute of Chemistry, Laboratory of Inorganic Synthesis and Crystallographypt_BR
dc.description.unidadeInstituto de Química (IQ)pt_BR
dc.description.unidadeFaculdade de Ciências e Tecnologias em Saúde (FCTS) – Campus UnB Ceilândiapt_BR
dc.description.unidadeColegiado de Bases Biológicas e da Saúde (FCTS-BASES)pt_BR
dc.description.ppgPrograma de Pós-Graduação em Químicapt_BR
dc.description.ppgPrograma de Pós-Graduação em Ciências e Tecnologias em Saúdept_BR
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