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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

, , , , , , , , , , and . J Med Chem, 52 (8): 2393-406 (April 2009)Franchetti, Palmarisa Cappellacci, Loredana Vita, Patrizia Petrelli, Riccardo Lavecchia, Antonio Kachler, Sonja Klotz, Karl-Norbert Marabese, Ida Luongo, Livio Maione, Sabatino Grifantini, Mario Research Support, Non-U.S. Gov't United States Journal of medicinal chemistry J Med Chem. 2009 Apr 23;52(8):2393-406..

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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, , , , , , , , , and 1 other author(s). J Med Chem, 52 (8): 2393-406 (April 2009)Franchetti, Palmarisa Cappellacci, Loredana Vita, Patrizia Petrelli, Riccardo Lavecchia, Antonio Kachler, Sonja Klotz, Karl-Norbert Marabese, Ida Luongo, Livio Maione, Sabatino Grifantini, Mario Research Support, Non-U.S. Gov't United States Journal of medicinal chemistry J Med Chem. 2009 Apr 23;52(8):2393-406..