Transnitrosation of nitrosothiols: Characterization of an elusive intermediate

We report an investigation of the reaction between (S)-nitroso-L-cysteine ethyl ester and L-cysteine ethyl ester as a model of physiologically relevant transnitrosation processes. Our theoretical and experimental evidence clearly supports the existence of a nitroxyl disulfide intermediate in solutio...

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Autores principales: Perissinotti, Laura L., Turjanski, Adrián Gustavo, Estrin, Dario Ariel, Doctorovich, Fabio Ariel
Publicado: 2005
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v127_n2_p486_Perissinotti
http://hdl.handle.net/20.500.12110/paper_00027863_v127_n2_p486_Perissinotti
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spelling paper:paper_00027863_v127_n2_p486_Perissinotti2023-06-08T14:22:41Z Transnitrosation of nitrosothiols: Characterization of an elusive intermediate Perissinotti, Laura L. Turjanski, Adrián Gustavo Estrin, Dario Ariel Doctorovich, Fabio Ariel nitrosocysteine ethylester thiol derivative unclassified drug article chemical reaction kinetics geometry nitrogen nuclear magnetic resonance nitrosation nuclear magnetic resonance spectroscopy proton nuclear magnetic resonance thermodynamics transnitrosation Cysteine Kinetics Magnetic Resonance Spectroscopy Models, Molecular Nitrosation Nitroso Compounds Thermodynamics We report an investigation of the reaction between (S)-nitroso-L-cysteine ethyl ester and L-cysteine ethyl ester as a model of physiologically relevant transnitrosation processes. Our theoretical and experimental evidence clearly supports the existence of a nitroxyl disulfide intermediate in solution. Copyright © 2005 American Chemical Society. Fil:Perissinotti, L.L. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Turjanski, A.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Estrin, D.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Doctorovich, F. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2005 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v127_n2_p486_Perissinotti http://hdl.handle.net/20.500.12110/paper_00027863_v127_n2_p486_Perissinotti
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic nitrosocysteine ethylester
thiol derivative
unclassified drug
article
chemical reaction kinetics
geometry
nitrogen nuclear magnetic resonance
nitrosation
nuclear magnetic resonance spectroscopy
proton nuclear magnetic resonance
thermodynamics
transnitrosation
Cysteine
Kinetics
Magnetic Resonance Spectroscopy
Models, Molecular
Nitrosation
Nitroso Compounds
Thermodynamics
spellingShingle nitrosocysteine ethylester
thiol derivative
unclassified drug
article
chemical reaction kinetics
geometry
nitrogen nuclear magnetic resonance
nitrosation
nuclear magnetic resonance spectroscopy
proton nuclear magnetic resonance
thermodynamics
transnitrosation
Cysteine
Kinetics
Magnetic Resonance Spectroscopy
Models, Molecular
Nitrosation
Nitroso Compounds
Thermodynamics
Perissinotti, Laura L.
Turjanski, Adrián Gustavo
Estrin, Dario Ariel
Doctorovich, Fabio Ariel
Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
topic_facet nitrosocysteine ethylester
thiol derivative
unclassified drug
article
chemical reaction kinetics
geometry
nitrogen nuclear magnetic resonance
nitrosation
nuclear magnetic resonance spectroscopy
proton nuclear magnetic resonance
thermodynamics
transnitrosation
Cysteine
Kinetics
Magnetic Resonance Spectroscopy
Models, Molecular
Nitrosation
Nitroso Compounds
Thermodynamics
description We report an investigation of the reaction between (S)-nitroso-L-cysteine ethyl ester and L-cysteine ethyl ester as a model of physiologically relevant transnitrosation processes. Our theoretical and experimental evidence clearly supports the existence of a nitroxyl disulfide intermediate in solution. Copyright © 2005 American Chemical Society.
author Perissinotti, Laura L.
Turjanski, Adrián Gustavo
Estrin, Dario Ariel
Doctorovich, Fabio Ariel
author_facet Perissinotti, Laura L.
Turjanski, Adrián Gustavo
Estrin, Dario Ariel
Doctorovich, Fabio Ariel
author_sort Perissinotti, Laura L.
title Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
title_short Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
title_full Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
title_fullStr Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
title_full_unstemmed Transnitrosation of nitrosothiols: Characterization of an elusive intermediate
title_sort transnitrosation of nitrosothiols: characterization of an elusive intermediate
publishDate 2005
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00027863_v127_n2_p486_Perissinotti
http://hdl.handle.net/20.500.12110/paper_00027863_v127_n2_p486_Perissinotti
work_keys_str_mv AT perissinottilaural transnitrosationofnitrosothiolscharacterizationofanelusiveintermediate
AT turjanskiadriangustavo transnitrosationofnitrosothiolscharacterizationofanelusiveintermediate
AT estrindarioariel transnitrosationofnitrosothiolscharacterizationofanelusiveintermediate
AT doctorovichfabioariel transnitrosationofnitrosothiolscharacterizationofanelusiveintermediate
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