Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.

Novel 8-substituted base and sugar-modified analogues of the Ca(2+) mobilizing second messenger cyclic adenosine 5'-diphosphate ribose (cADPR) were synthesized using a chemoenzymatic approach and evaluated for activity in sea urchin egg homogenate (SUH) and in Jurkat T-lymphocytes; conformation...

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Main Authors: Moreau, C, Ashamu, G, Bailey, VC, Galione, A, Guse, A, Potter, B
Format: Journal article
Language:English
Published: 2011
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author Moreau, C
Ashamu, G
Bailey, VC
Galione, A
Guse, A
Potter, B
author_facet Moreau, C
Ashamu, G
Bailey, VC
Galione, A
Guse, A
Potter, B
author_sort Moreau, C
collection OXFORD
description Novel 8-substituted base and sugar-modified analogues of the Ca(2+) mobilizing second messenger cyclic adenosine 5'-diphosphate ribose (cADPR) were synthesized using a chemoenzymatic approach and evaluated for activity in sea urchin egg homogenate (SUH) and in Jurkat T-lymphocytes; conformational analysis investigated by (1)H NMR spectroscopy revealed that a C2'endo/syn conformation of the "southern" ribose is crucial for agonist or antagonist activity at the SUH-, but not at the T cell-cADPR receptor.
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spelling oxford-uuid:4fb7f9c8-8eb4-4f89-9e07-d3df13f6d40e2022-03-26T16:09:05ZSynthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:4fb7f9c8-8eb4-4f89-9e07-d3df13f6d40eEnglishSymplectic Elements at Oxford2011Moreau, CAshamu, GBailey, VCGalione, AGuse, APotter, BNovel 8-substituted base and sugar-modified analogues of the Ca(2+) mobilizing second messenger cyclic adenosine 5'-diphosphate ribose (cADPR) were synthesized using a chemoenzymatic approach and evaluated for activity in sea urchin egg homogenate (SUH) and in Jurkat T-lymphocytes; conformational analysis investigated by (1)H NMR spectroscopy revealed that a C2'endo/syn conformation of the "southern" ribose is crucial for agonist or antagonist activity at the SUH-, but not at the T cell-cADPR receptor.
spellingShingle Moreau, C
Ashamu, G
Bailey, VC
Galione, A
Guse, A
Potter, B
Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.
title Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.
title_full Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.
title_fullStr Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.
title_full_unstemmed Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.
title_short Synthesis of cyclic adenosine 5'-diphosphate ribose analogues: a C2'endo/syn "southern" ribose conformation underlies activity at the sea urchin cADPR receptor.
title_sort synthesis of cyclic adenosine 5 diphosphate ribose analogues a c2 endo syn southern ribose conformation underlies activity at the sea urchin cadpr receptor
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