Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities
Autor(a) principal: | |
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Data de Publicação: | 1999 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Brazilian Journal of Medical and Biological Research |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011 |
Resumo: | 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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Brazilian Journal of Medical and Biological Research |
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Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activitiesnitric oxideS-nitrosothiols (thionitrites)antioxidantperoxynitriteNovel 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.Associação Brasileira de Divulgação Científica1999-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011Brazilian Journal of Medical and Biological Research v.32 n.11 1999reponame:Brazilian Journal of Medical and Biological Researchinstname:Associação Brasileira de Divulgação Científica (ABDC)instacron:ABDC10.1590/S0100-879X1999001100011info:eu-repo/semantics/openAccessPetit,C.Bernardes-Genisson,V.Hoffmann,P.Souchard,J.-P.Labidalle,S.eng1999-12-01T00:00:00Zoai:scielo:S0100-879X1999001100011Revistahttps://www.bjournal.org/https://old.scielo.br/oai/scielo-oai.phpbjournal@terra.com.br||bjournal@terra.com.br1414-431X0100-879Xopendoar:1999-12-01T00:00Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC)false |
dc.title.none.fl_str_mv |
Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities |
title |
Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities |
spellingShingle |
Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities Petit,C. nitric oxide S-nitrosothiols (thionitrites) antioxidant peroxynitrite |
title_short |
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_sort |
Novel donors of nitric oxide derived of S-nitrosocysteine possessing antioxidant activities |
author |
Petit,C. |
author_facet |
Petit,C. Bernardes-Genisson,V. Hoffmann,P. Souchard,J.-P. Labidalle,S. |
author_role |
author |
author2 |
Bernardes-Genisson,V. Hoffmann,P. Souchard,J.-P. Labidalle,S. |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Petit,C. Bernardes-Genisson,V. Hoffmann,P. Souchard,J.-P. Labidalle,S. |
dc.subject.por.fl_str_mv |
nitric oxide S-nitrosothiols (thionitrites) antioxidant peroxynitrite |
topic |
nitric oxide S-nitrosothiols (thionitrites) antioxidant peroxynitrite |
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. |
publishDate |
1999 |
dc.date.none.fl_str_mv |
1999-11-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X1999001100011 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0100-879X1999001100011 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
publisher.none.fl_str_mv |
Associação Brasileira de Divulgação Científica |
dc.source.none.fl_str_mv |
Brazilian Journal of Medical and Biological Research v.32 n.11 1999 reponame:Brazilian Journal of Medical and Biological Research instname:Associação Brasileira de Divulgação Científica (ABDC) instacron:ABDC |
instname_str |
Associação Brasileira de Divulgação Científica (ABDC) |
instacron_str |
ABDC |
institution |
ABDC |
reponame_str |
Brazilian Journal of Medical and Biological Research |
collection |
Brazilian Journal of Medical and Biological Research |
repository.name.fl_str_mv |
Brazilian Journal of Medical and Biological Research - Associação Brasileira de Divulgação Científica (ABDC) |
repository.mail.fl_str_mv |
bjournal@terra.com.br||bjournal@terra.com.br |
_version_ |
1754302930106712064 |