4.7 Article

Synthesis and spectroscopy of CoII, NiII, CuII and ZnII complexes derived from 3,5-disubstituted-1H-pyrazole derivative: A special emphasis on DNA binding and cleavage studies

Journal

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 45, Issue 2, Pages 455-462

Publisher

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.ejmech.2009.10.026

Keywords

3,5-Dichloroformyl-1H-pyrazole; Quinoxaline; Gel-electrophoresis; DNA; Biogram

Funding

  1. University Grants Commission, New Delhi, India
  2. Karnatak University, Dharwad, Karnataka, India

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A series of novel Co-II, Ni-II, Cu-II and Zn-II complexes of 1H-pyrazole-3,5-dicarboxylic(2'-hydroxy-3'-hydrazinequinoxaline) has been prepared and characterized by the spectral and analytical techniques. Cull ion reacts with the ligand LH3 and forms the complex in one compartment of the ligand whereas, the other compartment remains free. In Co-II, Ni-II and Zn-II complexes both compartments of LH3 are involved in the coordination. DNA binding/cleavage studies were revealed the stronger binding capability of the present Ni-II complex, confirmed by the absorbance, viscometric and gel-electrophoresis studies. Similarly, remaining complexes do the same in the ligand field with lesser binding constants, subsequently, no complex was found to cleave the DNA. Finally, Cu-II complex shows growth inhibitory activity against biogram. (C) 2009 Elsevier Masson SAS. All rights reserved.

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