Determination of the relative and absolute stereochemistry of a potent and alpha1A-selective adrenoceptor antagonist

Bioorg Med Chem Lett. 2000 Dec 18;10(24):2705-7. doi: 10.1016/s0960-894x(00)00524-2.

Abstract

The binding affinities and selectivities of antagonists 1-4 for the alpha1A-adrenoceptor are dependent on the stereochemical orientation of the groups at the C-4 and C-5 positions of the oxazolidinone ring. The unambiguous assignment of the relative and absolute configurations of the diastereomers of SNAP 7915 (1) is reported.

MeSH terms

  • Adrenergic alpha-1 Receptor Antagonists*
  • Adrenergic alpha-Antagonists / chemistry*
  • Nuclear Magnetic Resonance, Biomolecular
  • Oxazoles / chemistry
  • Stereoisomerism

Substances

  • Adrenergic alpha-1 Receptor Antagonists
  • Adrenergic alpha-Antagonists
  • Oxazoles
  • SNAP 7915