Journal
JOURNAL OF INORGANIC BIOCHEMISTRY
Volume 100, Issue 1, Pages 124-132Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2005.10.009
Keywords
oxythiamine complexes; vitamin B-1 antagonist; X-ray structure; Zn, Cd and Hg complexes; N-15 NMR spectroscopy
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The reaction of oxythiamine chloride hydrochloride (HOxTCl center dot HCl) with ZnCl2, CdCl2 and HgCl2 in ethanol yielded the complexes [ZnCl3(HOxT)], [CdCl3(HOxT)] and [HgCl3(HOxT)]. In water, the reaction with CdCl2 afforded [CdCl2(OxT)], but reaction with ZnCl2 or HgCl2 yielded unidentified products. The four new complexes were characterized by mass spectrometry and IR spectroscopy in the solid state and by H-1, C-13 and N-15 nuclear magnetic resonance (NMR) spectroscopy in hexadeuterated dimethylsulfoxide (DMSO-d(6)), and three were also studied by X-ray diffractometry. In [ZnCl3(HOxT)] and [HgCl3(HOxT)] the oxythiamine ligand is bound to the metal via N(1') and adopts the V conformation exhibited by thiamine in biological contexts. The infrared (IR) spectrum of [CdCl3(HOxT)] suggests a similar coordination mode. In [CdCl2(OxT)] each OxT zwitterion coordinates to one Cd(II) ion via its N(1') atom and to another via its N(3') and O atoms, giving rise to a polymeric chain along the x-axis. The coordination number of the metal is made up to six by Cd center dot center dot center dot Cl interactions, two of which link the polymeric chains in pairs. This seems to be the first metal complex containing the oxythiamine ligand as a zwitterion, with the N(3')-H/O(4'alpha)-H group deprotonated. Neither HOxTCl nor its zinc(II) complex showed any significant activity in vitro against HeLa cells. (C) 2005 Elsevier Inc. All rights reserved.
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