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Trends in Heterocyclic Chemistry   Volumes    Volume 1 
Abstract
Superoxide dismutase mimicking activity of copper (II) complexes of bis-(methylthio) and methylthio amino derivatives of 1 - methylpyridinium-(and quinolinium)-2-dithioacetic acids and other heterocyclic ligands
William O. Foye, Krishnendu Ghosh
Pages: 9 - 17
Number of pages: 9
Trends in Heterocyclic Chemistry
Volume 1 

Copyright © 1990 Research Trends. All rights reserved

ABSTRACT
 
Bis (methylthio) and methylthio amino derivatives of 1-methylpyridinium (and quinolinium)-2-dithioacetic acids, found to have protective activity in mice vs. lethal doses of γ-radiation, were converted to Cu(II) complexes. The complexes were isolated as double salts with CuCl2, and some were sufficiently soluble to be assayed for superoxide dismutase (SOD) activity. This was done by measuring the inhibition of the superoxide reduction of nitroblue tetrazolium. A positive correlation was found in both the pyridinium and quinolinium series between the extent of SOD activity and the degree of radiation protection. This provides evidence for a mechanism of whole body radiation protection, based on the ability to dismutate superoxide. Copper complexes of a variety of other heterocyclic ligands showed much less ability to mimic SOD activity.
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