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Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants

The generation of excess reactive oxygen species (ROS) in mitochondria is responsible for much of the oxidative stress associated with ageing (aging), and mitochondrial dysfunction is part of the pathology of neurodegeneration and type 2 diabetes. Lipophilic pyridinium ions are known to accumulate i...

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Detalles Bibliográficos
Autores principales: Robertson, Linsey, Hartley, Richard C.
Formato: Texto
Lenguaje:English
Publicado: Pergamon Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722452/
https://www.ncbi.nlm.nih.gov/pubmed/19693262
http://dx.doi.org/10.1016/j.tet.2009.04.083
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author Robertson, Linsey
Hartley, Richard C.
author_facet Robertson, Linsey
Hartley, Richard C.
author_sort Robertson, Linsey
collection PubMed
description The generation of excess reactive oxygen species (ROS) in mitochondria is responsible for much of the oxidative stress associated with ageing (aging), and mitochondrial dysfunction is part of the pathology of neurodegeneration and type 2 diabetes. Lipophilic pyridinium ions are known to accumulate in mitochondria and this paper describes a general route for the preparation of nitrone-containing N-arylpyridinium salts having a range of lipophilicities, as potential therapeutic antioxidants. The compatibility of nitrones with the Zincke reaction is the key to their synthesis. Their trapping of carbon-centred radicals and the EPR spectra of the resulting nitroxides are reported.
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spelling pubmed-27224522009-08-18 Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants Robertson, Linsey Hartley, Richard C. Tetrahedron Article The generation of excess reactive oxygen species (ROS) in mitochondria is responsible for much of the oxidative stress associated with ageing (aging), and mitochondrial dysfunction is part of the pathology of neurodegeneration and type 2 diabetes. Lipophilic pyridinium ions are known to accumulate in mitochondria and this paper describes a general route for the preparation of nitrone-containing N-arylpyridinium salts having a range of lipophilicities, as potential therapeutic antioxidants. The compatibility of nitrones with the Zincke reaction is the key to their synthesis. Their trapping of carbon-centred radicals and the EPR spectra of the resulting nitroxides are reported. Pergamon Press 2009-07-04 /pmc/articles/PMC2722452/ /pubmed/19693262 http://dx.doi.org/10.1016/j.tet.2009.04.083 Text en © 2009 Elsevier Ltd. https://creativecommons.org/licenses/by/3.0/Open Access under CC BY 3.0 (https://creativecommons.org/licenses/by/3.0/) license
spellingShingle Article
Robertson, Linsey
Hartley, Richard C.
Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
title Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
title_full Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
title_fullStr Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
title_full_unstemmed Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
title_short Synthesis of N-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
title_sort synthesis of n-arylpyridinium salts bearing a nitrone spin trap as potential mitochondria-targeted antioxidants
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722452/
https://www.ncbi.nlm.nih.gov/pubmed/19693262
http://dx.doi.org/10.1016/j.tet.2009.04.083
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