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Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities

Deprotonated glutathione is among the most potent biological nucleophiles and plays an important physiological role in cellular detoxification by forming covalent conjugates with Michael acceptors. The electrophilicity E of various Michael acceptors was characterized recently according to the Patz–M...

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Autores principales: Mayer, Robert J., Ofial, Armin R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899611/
https://www.ncbi.nlm.nih.gov/pubmed/31560405
http://dx.doi.org/10.1002/anie.201909803
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author Mayer, Robert J.
Ofial, Armin R.
author_facet Mayer, Robert J.
Ofial, Armin R.
author_sort Mayer, Robert J.
collection PubMed
description Deprotonated glutathione is among the most potent biological nucleophiles and plays an important physiological role in cellular detoxification by forming covalent conjugates with Michael acceptors. The electrophilicity E of various Michael acceptors was characterized recently according to the Patz–Mayr relation lg k (2)=s (N)(N+E). We now determined the nucleophilic reactivity (N, s (N)) of glutathione (GSH) in aqueous solution at 20 °C to connect published GSH reactivities (k (GSH)) with Mayr's electrophilicity scale (E). In this way, electrophilicities E of more than 70 Michael acceptors could be estimated, which can now be used to systematically predict novel reactions with the multitude of nucleophiles whose nucleophilicity parameters N/s (N) are known.
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spelling pubmed-68996112019-12-19 Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities Mayer, Robert J. Ofial, Armin R. Angew Chem Int Ed Engl Communications Deprotonated glutathione is among the most potent biological nucleophiles and plays an important physiological role in cellular detoxification by forming covalent conjugates with Michael acceptors. The electrophilicity E of various Michael acceptors was characterized recently according to the Patz–Mayr relation lg k (2)=s (N)(N+E). We now determined the nucleophilic reactivity (N, s (N)) of glutathione (GSH) in aqueous solution at 20 °C to connect published GSH reactivities (k (GSH)) with Mayr's electrophilicity scale (E). In this way, electrophilicities E of more than 70 Michael acceptors could be estimated, which can now be used to systematically predict novel reactions with the multitude of nucleophiles whose nucleophilicity parameters N/s (N) are known. John Wiley and Sons Inc. 2019-10-31 2019-12-02 /pmc/articles/PMC6899611/ /pubmed/31560405 http://dx.doi.org/10.1002/anie.201909803 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Mayer, Robert J.
Ofial, Armin R.
Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities
title Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities
title_full Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities
title_fullStr Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities
title_full_unstemmed Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities
title_short Nucleophilicity of Glutathione: A Link to Michael Acceptor Reactivities
title_sort nucleophilicity of glutathione: a link to michael acceptor reactivities
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899611/
https://www.ncbi.nlm.nih.gov/pubmed/31560405
http://dx.doi.org/10.1002/anie.201909803
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