N6-Cycloalkyl- AndN6-Bicycloalkyl-C5′(C2′)-modified Adenosine Derivatives as High-Affinity and Selective Agonists at the Human A1Adenosine Receptor With Antinociceptive Effects in Mice

Journal of Medicinal Chemistry - United States
doi 10.1021/jm900498h
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American Chemical Society (ACS)

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