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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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. |
format | Online Article Text |
id | pubmed-6899611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mayerrobertj nucleophilicityofglutathionealinktomichaelacceptorreactivities AT ofialarminr nucleophilicityofglutathionealinktomichaelacceptorreactivities |