Synthesis and purine receptor affinity of 6-oxopurine nucleosides and nucleotides containing (N)-methanocarba-pseudoribose rings

Citation
G. Ravi et al., Synthesis and purine receptor affinity of 6-oxopurine nucleosides and nucleotides containing (N)-methanocarba-pseudoribose rings, BIOORG MED, 11(17), 2001, pp. 2295-2300
Citations number
16
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
ISSN journal
0960894X → ACNP
Volume
11
Issue
17
Year of publication
2001
Pages
2295 - 2300
Database
ISI
SICI code
0960-894X(20010903)11:17<2295:SAPRAO>2.0.ZU;2-6
Abstract
6-Oxopurine derivatives containing a northern (N) methanocarba modification (i.e., fused cyclopropane and cyclopentane rings in place of the ribose) w ere synthesized and the adenosine receptor affinity measured. Guanine or hy poxanthine was coupled at the 7-position, or 1,3-diblitylxanthine was coupl ed at the 9-position. The pseudoribose ring was also substituted at the 5 ' -position with an N-methyluronamide or with phosphate groups. Published by Elsevier Science Ltd.