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‘Click cyclic ADP-ribose’: a neutral second messenger mimic
Analogues of the potent Ca(2+) releasing second messenger cyclic ADP-ribose (cADPR) with a 1,2,3-triazole pyrophosphate bioisostere were synthesised by click-mediated macrocyclisation. The ability to activate Ca(2+) release was surprisingly retained, and hydrolysis of cADPR by CD38 could also be inh...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Royal Society of Chemistry
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047616/ https://www.ncbi.nlm.nih.gov/pubmed/24452494 http://dx.doi.org/10.1039/c3cc49249d |
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author | Swarbrick, Joanna M. Graeff, Richard Garnham, Clive Thomas, Mark P. Galione, Antony Potter, Barry V. L. |
author_facet | Swarbrick, Joanna M. Graeff, Richard Garnham, Clive Thomas, Mark P. Galione, Antony Potter, Barry V. L. |
author_sort | Swarbrick, Joanna M. |
collection | PubMed |
description | Analogues of the potent Ca(2+) releasing second messenger cyclic ADP-ribose (cADPR) with a 1,2,3-triazole pyrophosphate bioisostere were synthesised by click-mediated macrocyclisation. The ability to activate Ca(2+) release was surprisingly retained, and hydrolysis of cADPR by CD38 could also be inhibited, illustrating the potential of this approach to design drug-like signalling pathway modulators. |
format | Online Article Text |
id | pubmed-4047616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-40476162014-06-06 ‘Click cyclic ADP-ribose’: a neutral second messenger mimic Swarbrick, Joanna M. Graeff, Richard Garnham, Clive Thomas, Mark P. Galione, Antony Potter, Barry V. L. Chem Commun (Camb) Chemistry Analogues of the potent Ca(2+) releasing second messenger cyclic ADP-ribose (cADPR) with a 1,2,3-triazole pyrophosphate bioisostere were synthesised by click-mediated macrocyclisation. The ability to activate Ca(2+) release was surprisingly retained, and hydrolysis of cADPR by CD38 could also be inhibited, illustrating the potential of this approach to design drug-like signalling pathway modulators. Royal Society of Chemistry 2014-03-07 2014-01-23 /pmc/articles/PMC4047616/ /pubmed/24452494 http://dx.doi.org/10.1039/c3cc49249d Text en This journal is © The Royal Society of Chemistry 2014 https://creativecommons.org/licenses/by-nc/2.0/uk/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/ (https://creativecommons.org/licenses/by-nc/2.0/uk/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Chemistry Swarbrick, Joanna M. Graeff, Richard Garnham, Clive Thomas, Mark P. Galione, Antony Potter, Barry V. L. ‘Click cyclic ADP-ribose’: a neutral second messenger mimic |
title | ‘Click cyclic ADP-ribose’: a neutral second messenger mimic
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title_full | ‘Click cyclic ADP-ribose’: a neutral second messenger mimic
|
title_fullStr | ‘Click cyclic ADP-ribose’: a neutral second messenger mimic
|
title_full_unstemmed | ‘Click cyclic ADP-ribose’: a neutral second messenger mimic
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title_short | ‘Click cyclic ADP-ribose’: a neutral second messenger mimic
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title_sort | ‘click cyclic adp-ribose’: a neutral second messenger mimic |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4047616/ https://www.ncbi.nlm.nih.gov/pubmed/24452494 http://dx.doi.org/10.1039/c3cc49249d |
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