Synthesis, Structural Characterization, and Biological Evaluation of Oxorhenium(V) Complexes with a Novel Type of Thiosemicarbazones Derived from N-[N `,N `-Dialkylamino(thiocarbonyl)]benzimidoyl Chlorides
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2009
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Resumo |
Reactions of N-[N`,N`-diethylamino(thiocarbonyl)]benzimidoyl chloride with 4,4-dialkylthiosemicarbazides give a novel class of thiosemicarbazides/thiosemicarbazones, H(2)L, which causes a remarkable reduction of cell growth in in vitro experiments. These strong antiproliferative effects are also observed for oxorhenium(V) complexes of the general composition [ReOCl(L)], which are formed by reactions of the potentially tridentate ligands with (NBu(4))[ReOCl(4)]. A systematic substitution of the alkyl groups in the thiosemicarbazone building blocks of the ligands do not significantly influence the biological activity of the metal complexes, while the replacement of the chloro ligand by a PPh(3) ligand (by the replacement of the oxo unit by a nitrido ligand) completely terminated the cytotoxicity of the metal complexes. government of Vietnam government of Vietnam DFG - Deutsche Forschungsgemeinschaft DFG - Deutsche Forschungsgemeinschaft[FOR 630] DAAD DAAD Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) CAPES FAPESP Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) |
Identificador |
INORGANIC CHEMISTRY, v.48, n.19, p.9356-9364, 2009 0020-1669 http://producao.usp.br/handle/BDPI/31829 10.1021/ic901160v |
Idioma(s) |
eng |
Publicador |
AMER CHEMICAL SOC |
Relação |
Inorganic Chemistry |
Direitos |
restrictedAccess Copyright AMER CHEMICAL SOC |
Palavras-Chave | #2-ACETYLPYRIDINE THIOSEMICARBAZONES #DERIVATIVES #AGENTS #CELLS #1-ACETYLISOQUINOLINE #2-ACETYLQUINOLINE #INHIBITORS #INVITRO #ACID #Chemistry, Inorganic & Nuclear |
Tipo |
article original article publishedVersion |