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Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels
Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na(V) ) channels. Since there is an urgent need for small molecule Na(V) channel ligands as novel therapeutics, clathrodin could represent an interesting lead compound. Therefore, clathrodin was reinvestigated fo...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4012458/ https://www.ncbi.nlm.nih.gov/pubmed/24714127 http://dx.doi.org/10.3390/md12042132 |
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author | Peigneur, Steve Žula, Aleš Zidar, Nace Chan-Porter, Fiona Kirby, Robert Madge, David Ilaš, Janez Kikelj, Danijel Tytgat, Jan |
author_facet | Peigneur, Steve Žula, Aleš Zidar, Nace Chan-Porter, Fiona Kirby, Robert Madge, David Ilaš, Janez Kikelj, Danijel Tytgat, Jan |
author_sort | Peigneur, Steve |
collection | PubMed |
description | Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na(V) ) channels. Since there is an urgent need for small molecule Na(V) channel ligands as novel therapeutics, clathrodin could represent an interesting lead compound. Therefore, clathrodin was reinvestigated for its potency and Na(V) channel subtype selectivity. Clathrodin and its synthetic analogues were subjected to screening on a broad range of Na(V) channel isoforms, both in voltage clamp and patch clamp conditions. Even though clathrodin was not found to exert any activity, some analogues were capable of modulating the Na(V) channels, hereby validating the pyrrole-2-aminoimidazole alkaloid structure as a core structure for future small molecule-based Na(V) channel modulators. |
format | Online Article Text |
id | pubmed-4012458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-40124582014-05-07 Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels Peigneur, Steve Žula, Aleš Zidar, Nace Chan-Porter, Fiona Kirby, Robert Madge, David Ilaš, Janez Kikelj, Danijel Tytgat, Jan Mar Drugs Article Clathrodin is a marine alkaloid and believed to be a modulator of voltage-gated sodium (Na(V) ) channels. Since there is an urgent need for small molecule Na(V) channel ligands as novel therapeutics, clathrodin could represent an interesting lead compound. Therefore, clathrodin was reinvestigated for its potency and Na(V) channel subtype selectivity. Clathrodin and its synthetic analogues were subjected to screening on a broad range of Na(V) channel isoforms, both in voltage clamp and patch clamp conditions. Even though clathrodin was not found to exert any activity, some analogues were capable of modulating the Na(V) channels, hereby validating the pyrrole-2-aminoimidazole alkaloid structure as a core structure for future small molecule-based Na(V) channel modulators. MDPI 2014-04-04 /pmc/articles/PMC4012458/ /pubmed/24714127 http://dx.doi.org/10.3390/md12042132 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Peigneur, Steve Žula, Aleš Zidar, Nace Chan-Porter, Fiona Kirby, Robert Madge, David Ilaš, Janez Kikelj, Danijel Tytgat, Jan Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels |
title | Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels |
title_full | Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels |
title_fullStr | Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels |
title_full_unstemmed | Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels |
title_short | Action of Clathrodin and Analogues on Voltage-Gated Sodium Channels |
title_sort | action of clathrodin and analogues on voltage-gated sodium channels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4012458/ https://www.ncbi.nlm.nih.gov/pubmed/24714127 http://dx.doi.org/10.3390/md12042132 |
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