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On the cytotoxic activity of Pd(II) complexes of N,N-disubstituted-N'-acyl thioureas.
Plutín, Ana M; Mocelo, Raúl; Alvarez, Anislay; Ramos, Raúl; Castellano, Eduardo E; Cominetti, Marcia R; Graminha, Angelica E; Ferreira, Antonio G; Batista, Alzir A.
Afiliación
  • Plutín AM; Laboratorio de Síntesis Orgánica, Facultad de Química, Universidad de La Habana, La Habana, Cuba. Electronic address: anap@fq.uh.cu.
  • Mocelo R; Laboratorio de Síntesis Orgánica, Facultad de Química, Universidad de La Habana, La Habana, Cuba.
  • Alvarez A; Laboratorio de Síntesis Orgánica, Facultad de Química, Universidad de La Habana, La Habana, Cuba.
  • Ramos R; Laboratorio de Síntesis Orgánica, Facultad de Química, Universidad de La Habana, La Habana, Cuba.
  • Castellano EE; Instituto de Química de São Carlos, Universidade de São Paulo, São Carlos, SP, Brazil.
  • Cominetti MR; Departamento de Gerontologia, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • Graminha AE; Departamento de Química, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • Ferreira AG; Departamento de Química, Universidade Federal de São Carlos, São Carlos, SP, Brazil.
  • Batista AA; Departamento de Química, Universidade Federal de São Carlos, São Carlos, SP, Brazil. Electronic address: daab@ufscar.br.
J Inorg Biochem ; 134: 76-82, 2014 May.
Article en En | MEDLINE | ID: mdl-24561278
The rational design of anticancer drugs is one of the most promising strategies for increasing their cytotoxicity and for minimizing their toxicity. Manipulation of the structure of ligands or of complexes represents a strategy for which is possible to modify the potential mechanism of their action against the cancer cells. Here we present the cytotoxicity of some new palladium complexes and our intention is to show the importance of non-coordinated atoms of the ligands in the cytotoxicity of the complexes. New complexes of palladium (II), with general formulae [Pd(PPh3)2(L)]PF6 or [PdCl(PPh3)(L)], where L=N,N-disubstituted-N'-acyl thioureas, were synthesized and characterized by elemental analysis, molar conductivity, melting points, IR, NMR((1)H, (13)C and (31)P{(1)H}) spectroscopy. The spectroscopic data are consistent with the complexes containing an O, S chelated ligand. The structures of complexes with N,N-dimethyl-N'-benzoylthiourea, N,N-diphenyl-N'-benzoylthiourea, N,N-diethyl-N'-furoylthiourea, and N,N-diphenyl-N'-furoylthiourea were determined by X-ray crystallography, confirming the coordination of the ligands with the metal through sulfur and oxygen atoms, forming distorted square-planar structures. The N,N-disubstituted-N'-acyl thioureas and their complexes were screened with respect to their antitumor cytotoxicity against DU-145 (human prostate cancer cells), MDA-MB-231 (human breast cancer cells) and their toxicity against the L929 cell line (health cell line from mouse).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paladio / Tiourea / Citotoxinas / Complejos de Coordinación / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: J Inorg Biochem Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Paladio / Tiourea / Citotoxinas / Complejos de Coordinación / Antineoplásicos Límite: Animals / Humans Idioma: En Revista: J Inorg Biochem Año: 2014 Tipo del documento: Article Pais de publicación: Estados Unidos