Síntese, atividade biológica e estudos de interação com biomoléculas de complexos metálicos de ligantes com interesse farmacológico
Ano de defesa: | 2016 |
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Autor(a) principal: | |
Orientador(a): | |
Banca de defesa: | |
Tipo de documento: | Tese |
Tipo de acesso: | Acesso aberto |
Idioma: | por |
Instituição de defesa: |
Universidade Federal de Minas Gerais
UFMG |
Programa de Pós-Graduação: |
Não Informado pela instituição
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Departamento: |
Não Informado pela instituição
|
País: |
Não Informado pela instituição
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Palavras-chave em Português: | |
Link de acesso: | http://hdl.handle.net/1843/SFSA-AVBMYG |
Resumo: | In the present work eight metal complexes were studied being four already related in the literature and, four new complexes. The new complexes were characterized using physicochemical and spectroscopic techniques: [CuCl2(H2O)(NOR)].H2O (1), [CuCl2(py)(NOR)].H2O(2), [CuCl(bipy)(NOR)]Cl.2H2O (3), [CuCl2(phen)(NOR)].3H2O (4), [AuS(CH3)2(NOR)]Cl (5), [Au(pyc)(NOR)2]2Cl.3H2O (6), [CuCl(L1)(phen)].0.5H2O (7) and [CuCl(L2)(phen)].2.5H2O (8),where NOR is the fluoroquinolone antibiotic norfloxacin, py = pyridine, bipy = 2,2- bipyridine, phen = 1,10-phenantroline, pyc = piridin-2-carboxilic acid and L1 and L2 represent the Schiff bases 2-((5-nitrofuran-2-il)metilamino)fenol and 2-(4-nitrobenzilidenoamino) fenol. Complexes 3, 4 and 7 showed promising activity against Tripanossoma cruzi, the causative agent of Chagas disease (0.94 - 16 µmol L-1), whereas 1-6 proved to be active againstdifferent bacteria strains. In some cases, however, the free NOR demonstrated superior activity. Complexes 7 and 8 were active against seven cancer cell lines in doses lower than 2 µg mL-1 (or 3.4 µmol L-1), whilst 7 also showed antifungal activity in some fungi strains.Complexes 1-8 interacted with DNA on a scale of weak to moderate (Kb 103-104). The interaction of complexes 1, 7 and 8 with DNA, which was perhaps due to intercalation, whilst the other complexes probably interacted with the DNA's external structure. Complexes 1-4, 7 and 8 Interacted with the bovine (BSA) and human (HSA) serum albumins.These interactions were moderate and occurred, at least in part, through a static mechanism. Complexes 5 and 6 interacted with HSA through a mainly dynamic and static mechanism respectively. The negative values of Gibbs free energy ([delta]G) showed that 5 and 6 interacted spontaneously with HSA. |