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The synthesis of highly potent, selective, and water-soluble agonists at the human adenosine A3 receptor
Authors:DeNinno Michael P  Masamune Hiroko  Chenard Lois K  DiRico Kenneth J  Eller Cynthia  Etienne John B  Tickner Jeanene E  Kennedy Scott P  Knight Delvin R  Kong Jimmy  Oleynek Joseph J  Tracey W Ross  Hill Roger J
Institution:Pfizer Global Research and Development, Groton/NewLondon Laboratories, Groton, CT 06340, USA. michael.p.deninno@pfizer.com
Abstract:Using a combination of parallel and directed synthesis, the discovery of a highly potent and selective series of adenosine A3 agonists was achieved. High aqueous solubility, required for the intended parenteral route of administration, was achieved by the presence of one or two basic amine functional groups.
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