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Selective small-molecule EPAC activators
The cellular signalling enzymes, EPAC1 and EPAC2, have emerged as key intracellular sensors of the secondary messenger cyclic 3′,5′-adenosine monophosphate (cyclic adenosine monophosphate) alongside protein kinase A. Interest has been galvanised in recent years thanks to the emergence of these speci...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824682/ https://www.ncbi.nlm.nih.gov/pubmed/31671184 http://dx.doi.org/10.1042/BST20190254 |
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author | Luchowska-Stańska, Urszula Morgan, David Yarwood, Stephen J. Barker, Graeme |
author_facet | Luchowska-Stańska, Urszula Morgan, David Yarwood, Stephen J. Barker, Graeme |
author_sort | Luchowska-Stańska, Urszula |
collection | PubMed |
description | The cellular signalling enzymes, EPAC1 and EPAC2, have emerged as key intracellular sensors of the secondary messenger cyclic 3′,5′-adenosine monophosphate (cyclic adenosine monophosphate) alongside protein kinase A. Interest has been galvanised in recent years thanks to the emergence of these species as potential targets for new cardiovascular disease therapies, including vascular inflammation and insulin resistance in vascular endothelial cells. We herein summarise the current state-of-the-art in small-molecule EPAC activity modulators, including cyclic nucleotides, sulphonylureas, and N-acylsulphonamides. |
format | Online Article Text |
id | pubmed-6824682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68246822019-11-12 Selective small-molecule EPAC activators Luchowska-Stańska, Urszula Morgan, David Yarwood, Stephen J. Barker, Graeme Biochem Soc Trans Review Articles The cellular signalling enzymes, EPAC1 and EPAC2, have emerged as key intracellular sensors of the secondary messenger cyclic 3′,5′-adenosine monophosphate (cyclic adenosine monophosphate) alongside protein kinase A. Interest has been galvanised in recent years thanks to the emergence of these species as potential targets for new cardiovascular disease therapies, including vascular inflammation and insulin resistance in vascular endothelial cells. We herein summarise the current state-of-the-art in small-molecule EPAC activity modulators, including cyclic nucleotides, sulphonylureas, and N-acylsulphonamides. Portland Press Ltd. 2019-10-31 2019-10-11 /pmc/articles/PMC6824682/ /pubmed/31671184 http://dx.doi.org/10.1042/BST20190254 Text en © 2019 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Articles Luchowska-Stańska, Urszula Morgan, David Yarwood, Stephen J. Barker, Graeme Selective small-molecule EPAC activators |
title | Selective small-molecule EPAC activators |
title_full | Selective small-molecule EPAC activators |
title_fullStr | Selective small-molecule EPAC activators |
title_full_unstemmed | Selective small-molecule EPAC activators |
title_short | Selective small-molecule EPAC activators |
title_sort | selective small-molecule epac activators |
topic | Review Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824682/ https://www.ncbi.nlm.nih.gov/pubmed/31671184 http://dx.doi.org/10.1042/BST20190254 |
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