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)(...

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Main Authors: C. Petit, V. Bernardes-Genisson, P. Hoffmann, J.-P. Souchard, S. Labidalle
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 1999-11-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011
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author C. Petit
V. Bernardes-Genisson
P. Hoffmann
J.-P. Souchard
S. Labidalle
author_facet C. Petit
V. Bernardes-Genisson
P. Hoffmann
J.-P. Souchard
S. Labidalle
author_sort C. Petit
collection DOAJ
description 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.
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spelling doaj.art-eb3a148de90a4d8db84cc025132fcc7a2022-12-21T22:50:44ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research0100-879X1414-431X1999-11-0132111407141210.1590/S0100-879X1999001100011Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activitiesC. PetitV. Bernardes-GenissonP. HoffmannJ.-P. SouchardS. LabidalleNovel 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011nitric oxideS-nitrosothiols (thionitrites)antioxidantperoxynitrite
spellingShingle C. Petit
V. Bernardes-Genisson
P. Hoffmann
J.-P. Souchard
S. Labidalle
Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
Brazilian Journal of Medical and Biological Research
nitric oxide
S-nitrosothiols (thionitrites)
antioxidant
peroxynitrite
title Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
title_full Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
title_fullStr Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
title_full_unstemmed Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
title_short Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
title_sort novel donors of nitric oxide derived of s nitrosocysteine possessing antioxidant activities
topic nitric oxide
S-nitrosothiols (thionitrites)
antioxidant
peroxynitrite
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011
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AT phoffmann noveldonorsofnitricoxidederivedofsnitrosocysteinepossessingantioxidantactivities
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