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      Adenosine receptors as drug targets--what are the challenges?

      Nature reviews. Drug discovery
      Adenosine A2 Receptor Agonists, pharmacology, Animals, Drug Approval, Drug Design, Humans, Molecular Targeted Therapy, Purines, Pyrazoles, Receptors, Purinergic P1, drug effects, metabolism, Signal Transduction, United States, United States Food and Drug Administration

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          Abstract

          Adenosine signalling has long been a target for drug development, with adenosine itself or its derivatives being used clinically since the 1940s. In addition, methylxanthines such as caffeine have profound biological effects as antagonists at adenosine receptors. Moreover, drugs such as dipyridamole and methotrexate act by enhancing the activation of adenosine receptors. There is strong evidence that adenosine has a functional role in many diseases, and several pharmacological compounds specifically targeting individual adenosine receptors--either directly or indirectly--have now entered the clinic. However, only one adenosine receptor-specific agent--the adenosine A2A receptor agonist regadenoson (Lexiscan; Astellas Pharma)--has so far gained approval from the US Food and Drug Administration (FDA). Here, we focus on the biology of adenosine signalling to identify hurdles in the development of additional pharmacological compounds targeting adenosine receptors and discuss strategies to overcome these challenges.

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