Abstract
<i>N</i><sup>6</sup>-Cycloalkyl- and <i>N</i><sup>6</sup>-Bicycloalkyl-<i>C</i>5′(<i>C</i>2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A<sub>1</sub> Adenosine Receptor with Antinociceptive Effects in Mice
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