Fused aminotetralins: novel antagonists with high selectivity for the dopamine D3 receptor

Bioorg Med Chem Lett. 1998 Oct 20;8(20):2859-64. doi: 10.1016/s0960-894x(98)00512-5.

Abstract

Starting from a series of 2-aminotetralins 1, a novel series of N-[4-(4-phenylbenzoylamino)butyl]-octahydrobenzoquinolines and hexahydrobenzoindoles with high potency and selectivity for the dopamine D3 receptor has been designed. The effect of ligand chirality on binding affinity has been established. Selected derivatives (e.g. 2o, 2p) show high functional selectivity and enhanced in vivo properties compared to 1.

MeSH terms

  • Animals
  • Dopamine D2 Receptor Antagonists*
  • Metabolic Clearance Rate
  • Rats
  • Receptors, Dopamine D3
  • Tetrahydronaphthalenes / chemistry*
  • Tetrahydronaphthalenes / pharmacokinetics
  • Tetrahydronaphthalenes / pharmacology

Substances

  • Dopamine D2 Receptor Antagonists
  • Drd3 protein, rat
  • Receptors, Dopamine D3
  • Tetrahydronaphthalenes
  • 2-aminotetralin