1141934-36-2Relevant academic research and scientific papers
N6-cycloalkyl- And n6-bicycloalkyl-c5'(c 2')-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice
Franchetti, Palmarisa,Cappellacci, Loredana,Vita, Patrizia,Petrelli, Riccardo,Lavecchia, Antonio,Kachler, Sonja,Klotz,Marabese, Ida,Luongo, Livio,Maione, Sabatino,Grifantini, Mario
experimental part, p. 2393 - 2406 (2010/04/30)
To further investigate new potent and selective human A1 adenosine receptor agonists, we have synthesized a series of 5'-chloro-5'-deoxy- and 5'-(2-fluorophenylthio)-5'-deoxy-N6-cycloalkyl(bicycloalkyl)- substituted adenosine and 2'-C-methylade
