Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities

Novel S-nitrosothiols possessing a phenolic function were investigated as nitric oxide (NO) donors. A study of NO release from these derivatives was carried out by electron spin resonance (ESR). All compounds gave rise to a characteristic three-line ESR signal in the presence of the complex [Fe(II)(MGD)2], revealing the formation of the complex [Fe(II)(MGD)2(NO)]. Furthermore, tests based on cytochrome c reduction were performed in order to study the ability of each phenolic disulfide, the final organic decomposition product of S-nitrosothiols, to trap superoxide radical anion (O2-). This study revealed a high reactivity of 1b and 3b towards O2-. For these two compounds, the respective inhibitory concentration (IC) 50 values were 92 µM and 43 µM.

Bibliographic Details

Main Authors:	Petit,C., Bernardes-Genisson,V., Hoffmann,P., Souchard,J.-P., Labidalle,S.
Format:	Digital revista
Language:	English
Published:	Associação Brasileira de Divulgação Científica 1999
Online Access:	http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011
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