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

Nat Rev Drug Discov. 2013 Apr;12(4):265-86. doi: 10.1038/nrd3955.

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.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

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

Substances

  • Adenosine A2 Receptor Agonists
  • Purines
  • Pyrazoles
  • Receptors, Purinergic P1
  • regadenoson