Issue 12, 2008

Synthesis, crystal structure, theoretical calculation and cytotoxic effect of new Pt(ii), Pd(ii) and Cu(ii) complexes with pyridine-pyrazoles derivatives

Abstract

The synthesis, structure and cytotoxic activity of Pt(II), Pd(II) and Cu(II) complexes of the general formula MLCl2 (M = Pt, Pd, Cu) 2–4 and (CuLCl2)25 where L is pyrazole-based chelate ligand 3-methyl-1-(2-pyridinyl)-1H-chromene[4,3-c]pyrazol-4-one 1 are described. The complexes were characterized by elemental analysis, infrared and 1H NMR spectroscopy, as well as electrospray mass spectrometry. Compounds 3 and 5 were also studied using X-ray diffraction. In addition, geometries, partial atomic charges, and lipophilicity, which determines their ability to penetrate through cells membranes, were obtained computationally. Complexes 2–4 exhibit square-planar geometries around the metal(II) centers and adopt cis configuration. Complex 5 is a dimer with distorted tetragonal pyramidal configuration at both Cu(II) centers, which are connected by two μ2-chloro bridges in axial positions. The cytotoxic effect of these complexes was examined on HL-60 and NALM-6 human leukemia cells and melanoma WM-115 cells. The Pt-complex cis-2 exhibited moderate cytotoxic activity against leukemic cells, but relatively high activity toward melanoma cells with cytotoxicity of IC50 = 16.6 μM at a level comparable to that of cisplatin (18.2 μM).

Graphical abstract: Synthesis, crystal structure, theoretical calculation and cytotoxic effect of new Pt(ii), Pd(ii) and Cu(ii) complexes with pyridine-pyrazoles derivatives

Supplementary files

Article information

Article type
Paper
Submitted
16 May 2008
Accepted
01 Jul 2008
First published
10 Sep 2008

New J. Chem., 2008,32, 2238-2244

Synthesis, crystal structure, theoretical calculation and cytotoxic effect of new Pt(II), Pd(II) and Cu(II) complexes with pyridine-pyrazoles derivatives

E. Budzisz, I. Lorenz, P. Mayer, P. Paneth, L. Szatkowski, U. Krajewska, M. Rozalski and M. Miernicka, New J. Chem., 2008, 32, 2238 DOI: 10.1039/B808301K

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