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Issue 13, 1995
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Chemoenzymatic synthesis of analogues of the second messenger candidate cyclic adenosine 5′-diphosphate ribose

Abstract

A broad substrate specificity for adenosine 5′-diphosphate ribosyl cyclase is demonstrated by cyclisation of ribose-and purine-modified nicotinamide adenine dinucleotide analogues to mimics of cyclic adenosine 5′-diphosphate ribose, generating a straightforward route for structural modification of this important Ca2+-mobilising nucleotide.

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Article information


J. Chem. Soc., Chem. Commun., 1995, 1359-1360
Article type
Paper

Chemoenzymatic synthesis of analogues of the second messenger candidate cyclic adenosine 5′-diphosphate ribose

G. A. Ashamu, A. Galione and B. V. L. Potter, J. Chem. Soc., Chem. Commun., 1995, 1359
DOI: 10.1039/C39950001359

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