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3,5-diacetyl-1,2,4-triazol bis(4N-substituted thiosemicarbazone) palladium(II) complexes: synthesis, structure, antiproliferative activity and low toxicity on normal kidney cells
Authors:Matesanz Ana I  Hernández Carolina  Rodríguez Ana  Souza Pilar
Affiliation:
  • a Departamento de Química Inorgánica (Módulo 07), Facultad de Ciencias, c/ Francisco Tomás y Valiente n° 7, Universidad Autónoma de Madrid, 28049-Madrid, Spain
  • b Departamento de Química Inorgánica, Orgánica y Bioquímica, Facultad de Ciencias del Medio Ambiente, Avd. Carlos III s/n, Universidad de Castilla-La Mancha, 45071-Toledo, Spain
  • c Departamento de Química Inorgánica, Orgánica y Bioquímica, ETS Ingenieros Industriales, Avd. Camilo José Cela n° 3, Universidad de Castilla-La Mancha, 13071-Ciudad Real, Spain
  • Abstract:Treatment of 4N-monosubstituted bis(thiosemicarbazone) ligands of 3,5-diacetyl-1,2,4-triazol series with lithium tetrachloridopalladate gave the dinuclear complexes of general formula [Pd(μ-H3L1-5)]2, but using dichloridobistriphenylphosphinepalladium(II) salt, the first mononuclear bis(thiosemicarbazone)-palladium-triphenylphosphine complexes of the 3,5-diacetyl-1,2,4-triazol series, [Pd(H3L1-5)PPh3], have been obtained. All the compounds have been characterized by elemental analysis and by IR and NMR spectroscopy, and the crystal and molecular structures of dinuclear complexes [Pd(μ-H3L3)]2 and [Pd(μ-H3L5)]2 as well as mononuclear complexes [Pd(H3L1)PPh3], [Pd(H3L2)PPh3], [Pd(H3L3)PPh3] and [Pd(H3L4)PPh3] have been determined by X-ray crystallography. The new compounds synthesized have been evaluated for antiproliferative activity in vitro against NCI-H460, A2780 and A2780cisR human cancer cell lines. Subsequent toxicity study, on normal renal LLC-PK1 cells, shows that all compounds investigated exhibit very low toxicity on kidney cells with respect to cisplatin.
    Keywords:Antitumour agents   Palladium complexes   Renal toxicity   Thiosemicarbazone   1,2,4-Triazol   X-ray diffraction
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