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http://hdl.handle.net/1843/71978
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DC Field | Value | Language |
---|---|---|
dc.creator | Darliane Aparecida Martins | pt_BR |
dc.creator | Lucius Flavius Ourives Bomfim Filho | pt_BR |
dc.creator | Cleiton Moreira da Silva | pt_BR |
dc.creator | Ângelo de Fátima | pt_BR |
dc.creator | Sônia Renaux Wanderley Louro | pt_BR |
dc.creator | Denise da Gama Jaen Batista | pt_BR |
dc.creator | Maria de Nazaré Correia Soeiro | pt_BR |
dc.creator | João Ernesto de Carvalho | pt_BR |
dc.creator | Letícia Regina de Souza Teixeira | pt_BR |
dc.date.accessioned | 2024-07-26T23:33:46Z | - |
dc.date.available | 2024-07-26T23:33:46Z | - |
dc.date.issued | 2017 | - |
dc.citation.volume | 28 | pt_BR |
dc.citation.issue | 1 | pt_BR |
dc.citation.spage | 87 | pt_BR |
dc.citation.epage | 97 | pt_BR |
dc.identifier.doi | http://dx.doi.org/10.5935/0103-5053.20160150 | pt_BR |
dc.identifier.issn | 0103-5053 | pt_BR |
dc.identifier.uri | http://hdl.handle.net/1843/71978 | - |
dc.description.resumo | Copper(II) complexes of the Schiff base ligands 2-((5-nitrofuran-2-yl)methyleneamino)phenol (HL1) and 2-(4-nitrobenzylideneamino)phenol (HL2) were prepared and characterized using physicochemical and spectroscopic techniques. In these complexes the Schiff base ligands acted as a bidentate donor bound to Cu2+ through the oxygen and nitrogen atoms in the deprotonated form. The electron paramagnetic resonance spectra, carried out on [CuCl(L1)(phen)].0.5H2O and [CuCl(L2)(phen)].2H2O complexes, showed the presence of only mononuclear forms. The Cu2+ complexes and ligands were evaluated for their in vitro trypanocidal activity. The complex [CuCl(L1)(phen)].0.5H2O was more active than the free Schiff base and also presented a superior effect to benznidazole, the reference drug. The antiproliferative activity of the Schiff bases and Cu2+ complexes were evaluated for their effect on seven tumor cell lines and showed a cytostatic and in some cases a cytotoxic effect. These compounds also presented binding properties to deoxyribonucleic acid (DNA) and moderate ability to quench the intrinsic fluorescence of albumins. | pt_BR |
dc.description.sponsorship | CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico | pt_BR |
dc.description.sponsorship | FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais | pt_BR |
dc.description.sponsorship | FAPERJ - Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro | pt_BR |
dc.description.sponsorship | Outra Agência | pt_BR |
dc.format.mimetype | pt_BR | |
dc.language | eng | pt_BR |
dc.publisher | Universidade Federal de Minas Gerais | pt_BR |
dc.publisher.country | Brasil | pt_BR |
dc.publisher.department | ICX - DEPARTAMENTO DE QUÍMICA | pt_BR |
dc.publisher.initials | UFMG | pt_BR |
dc.relation.ispartof | Journal of the Brazilian Chemical Society | pt_BR |
dc.rights | Acesso Aberto | pt_BR |
dc.subject | Schiff base | pt_BR |
dc.subject | Copper(II) complexes | pt_BR |
dc.subject | Biological activity | pt_BR |
dc.subject | DNA | pt_BR |
dc.subject | Albumin | pt_BR |
dc.subject.other | Schiff, Bases de | pt_BR |
dc.subject.other | Compostos de cobre | pt_BR |
dc.subject.other | Testes biológicos | pt_BR |
dc.subject.other | DNA | pt_BR |
dc.subject.other | Albumina | pt_BR |
dc.title | Copper(II) nitroaromatic schiff base complexes: synthesis, biological activity and their interaction with dna and albumins | pt_BR |
dc.type | Artigo de Periódico | pt_BR |
dc.url.externa | https://jbcs.sbq.org.br/default.asp?ed=247 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0001-5102-4633 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0001-9913-8971 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0003-2344-5590 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0001-5208-4144 | pt_BR |
dc.identifier.orcid | https://orcid.org/0000-0003-3790-572X | pt_BR |
Appears in Collections: | Artigo de Periódico |
Files in This Item:
File | Description | Size | Format | |
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Copper(II) Nitroaromatic Schiff Base Complexes- Synthesis, Biological Activity and (1).pdf | 555.21 kB | Adobe PDF | View/Open |
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