Synthesis and pharmacological characterization of beta2-adrenergic agonist enantiomers: zilpaterol

J Med Chem. 2009 Mar 26;52(6):1773-7. doi: 10.1021/jm801211c.

Abstract

The beta-adrenergic agonist 1 (zilpaterol) is used as production enhancer in cattle. Binding experiments of separated enantiomers on recombinant human beta(2)-adrenergic and mu-opioid receptors and functional studies showed that the (-)-1 enantiomer accounts for essentially all the beta(2)-adrenergic agonist activity and that it exhibits less affinity toward the mu-opioid receptor than (+)-1, which is a mu-opioid receptor antagonist. X-ray crystallography revealed the absolute configuration of (-)-1 to be 6R,7R.

MeSH terms

  • Adrenergic beta-2 Receptor Agonists*
  • Adrenergic beta-Agonists / chemical synthesis*
  • Adrenergic beta-Agonists / pharmacology*
  • Chromatography, High Pressure Liquid
  • Crystallography, X-Ray
  • Humans
  • Recombinant Proteins / agonists
  • Stereoisomerism
  • Trimethylsilyl Compounds / chemical synthesis*
  • Trimethylsilyl Compounds / pharmacology*

Substances

  • Adrenergic beta-2 Receptor Agonists
  • Adrenergic beta-Agonists
  • Recombinant Proteins
  • Trimethylsilyl Compounds
  • Zilpaterol