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Unusual entry to the novel 8-halo-N1-ribosyl hypoxanthine system by degradation of a cyclic adenosine-5'-diphosphate ribose analogue.
Moreau, Christelle; Woodman, Timothy J; Potter, Barry V L.
Affiliation
  • Moreau C; Wolfson Laboratory of Medicinal Chemistry, Department of Pharmacy and Pharmacology, University of Bath, Claverton Down, Bath, UK BA2 7AY.
Chem Commun (Camb) ; (10): 1127-9, 2006 Mar 14.
Article in En | MEDLINE | ID: mdl-16514461
ABSTRACT
Cyclic 8-bromo-inosine-5'-diphosphate ribose (8-Br-N1-cIDPR) was cleanly degraded at acidic pH by N9 ribosyl scission and subsequent pyrophosphate cleavage to give 8-bromo-N1-ribosyl hypoxanthine 5'-monophosphate (8-Br-N1-IMP), a novel class of mononucleotide, as the sole product.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Phosphates / Hypoxanthine / Cyclic ADP-Ribose Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2006 Document type: Article
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Phosphates / Hypoxanthine / Cyclic ADP-Ribose Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2006 Document type: Article
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