N6-cycloalkyl- and N6-bicycloalkyl- C5′(C2′)-modified adenosine derivatives as high-affinity and selective agonists at the human A1 adenosine receptor with antinociceptive effects in mice (Journal of Medicinal Chemistry)

Franchetti P.;Cappellacci L.;Vita P.;Petrelli R.;Lavecchia A.;Kachler S.;Klotz K. -N.;Marabese I.;Luongo L.;Maione S.;Grifantini M.

2009