The synthesis of highly potent, selective, and water-soluble agonists at the human adenosine A3 receptor

Bioorg Med Chem Lett. 2006 May 1;16(9):2525-7. doi: 10.1016/j.bmcl.2006.01.088. Epub 2006 Feb 7.

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.

MeSH terms

  • Adenosine / analogs & derivatives
  • Adenosine / chemical synthesis*
  • Adenosine / pharmacology*
  • Adenosine A3 Receptor Agonists*
  • Humans
  • Molecular Conformation
  • Solubility
  • Stereoisomerism
  • Structure-Activity Relationship
  • Water / chemistry

Substances

  • Adenosine A3 Receptor Agonists
  • Water
  • Adenosine