3,5-Dimethyl-1-thiocarbamoylpyrazole and its Pd(II) complexes: Synthesis, spectral studies and antitumor activity


Autoria(s): Rocha, F. V.; Barra, C. V.; Netto, Adelino Vieira de Godoy; Mauro, Antonio Eduardo; Carlos, I. Z.; Frem, Regina Célia Galvão; Ananias, S. R.; Quilles, M. B.; Stevanato, A.; da Rocha, M. C.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/05/2010

Resumo

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Complexes of the type [PdX(2)(tdmPz)] {X = Cl(-)(1) Br(-)(2); l(-)(3); SCN(-)(4); tdmPz = 1-thiocarbamoy1-3,5-dimethylpyrazole} have been synthesized and characterized. Compound 1 was formed from the reaction between [PdCl(2)(CH(3)CN)(2)] and 1-thiocarbamoy1-3,5-dimethylpyrazole. Complexes 2, 3 and 4 were obtained by metathesis of the chloro groups from 1 by bromide, iodide and thiocyanate ions, respectively. All the compounds and cisplatin have been tested in vitro by WIT assay for their cytotoxicity against three murine cancer cell lines: mammary adenocarcinoma (LM3 and LMM3) and lung adenocarcinoma (LP07) as well towards normal murine peritoneal exudate cells (PEC). Promising cytotoxic effect against LM3 has been found for 3 showing IC(50) equal to 24.5 mu M which is comparable to the value obtained for cisplatin (30.3 mu M). (C) 2010 Elsevier Masson SAS. All rights reserved.

Formato

1698-1702

Identificador

http://dx.doi.org/10.1016/j.ejmech.2009.12.073

European Journal of Medicinal Chemistry. Paris: Elsevier France-editions Scientifiques Medicales Elsevier, v. 45, n. 5, p. 1698-1702, 2010.

0223-5234

http://hdl.handle.net/11449/7337

10.1016/j.ejmech.2009.12.073

WOS:000276695200002

Idioma(s)

eng

Publicador

Elsevier France-editions Scientifiques Medicales Elsevier

Relação

European Journal of Medicinal Chemistry

Direitos

closedAccess

Palavras-Chave #Pd(II) complexes #1-Thiocarbamoyl-3,5-dimethylpyrazole #Spectroscopy #Antitumor activity
Tipo

info:eu-repo/semantics/article