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Bioinorg Chem Appl. 2003; 1(3-4): 271–284.
PMCID: PMC2267062
Synthesis, Characterization and Antitumor Activity of cis-bis(acylthioureato) platinum(II) Complexes, cis-[PtL2] [HL1=N,N-Diphenyl-N'-Benzoylthiourea or HL2=N,N-diphenyl-N'-(p-nitrobenzoyl)thiourea]
Wilfredo Hernández,1 Evgenia Spodine,corresponding author1 Juan Carlos Muñoz,2 Lothar Beyer,3 Uwe Schröder,3 Jorge Ferreira,4 and Mario Pavani4
1 Universidad de Chile, Facultad de Ciencias Químicas y Farmacéuticas, Santiago 1, Casilla 233, Chile,
2 Universidad de Chile, Facultad de Ciencias Físicas y Matemáticas, Santiago 1, Casilla 233, Chile,
3 Universität Leipzig, Institut für Anorganische Chemie, Johannisallee 29, Leipzig, D-04103, Germany,
4 Universidad de Chile, Instituto de Ciencias Biomédicas, Programa de Farmacología Clínica y Molecular, Facultad de Medicina, Santiago 1, Casilla 233, Chile,
Evgenia Spodine, espodine/at/ciq.uchile.cl.
corresponding authorCorresponding author.
Abstract
A low-molecular weight chromium-containing fraction of the material resulting from dichromate reduction by bovine liver homogenate was investigated by NMR and ES-MS. The ES-MS spectrum showed a readily detectable peak at m/z 786.1. The same molecular weight reasonably agreed with the relatively low diffusion coefficient measured by NMR-DOSY experiments on the main species observed in the 1H NMR spectrum. At least two downfield shifted and broad paramagnetic signals were apparent in the 1H NMR spectrum. Temperature dependence of chemical shift was exploited in order to estimate the diamagnetic shift of the signals in the diamagnetic region of the spectrum. 2D TOCSY, NOESY, COSY and 1H-13C HMQC spectra revealed the presence of aromatic protons (which were assigned as His residues), Gly and some other short chain amino-acids. Combinations of the molecular masses of such components together with acetate (which is present in the solution) and chromium atoms allowed a tentative proposal of a model for the compound.
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