[3H]S33084: a novel, selective and potent radioligand at cloned, human dopamine D3 receptors

Naunyn Schmiedebergs Arch Pharmacol. 2000 May;361(5):569-72. doi: 10.1007/s002100000217.

Abstract

The novel, selective dopamine D3 receptor antagonist, S33084 [(3aR,9bS)-N[4-(8-cyano- 1,3a,4,9b-tetrahydro-3H-benzopyrano[3,4-c]pyrrole-2-yl)-butyl] (4-phenyl)benzamide], was tritium-labelled to 59 Ci/mmol specific activity. Determination of association and dissociation rate constants at recombinant, human (h) D3 receptors stably expressed in Chinese hamster ovary (CHO) cells yielded a Kd value (0.16 nM) comparable to that observed in saturation binding experiments (0.17 nM). The competition binding profile of [3H]S33084 with diverse D3 receptor agonists and antagonists correlated highly (0.99) with that of [3H]spiperone. In conclusion, [3H]S33084 is a highly potent and selective radioligand at dopamine D3 receptors, which should be of considerable use for their characterisation.

MeSH terms

  • Animals
  • Benzopyrans / pharmacology*
  • Binding, Competitive
  • CHO Cells
  • Cells, Cultured
  • Cricetinae
  • Dopamine Antagonists / pharmacology*
  • Humans
  • Pyrroles / pharmacology*
  • Radioligand Assay
  • Receptors, Dopamine D2 / drug effects
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D2 / metabolism*
  • Receptors, Dopamine D3
  • Recombinant Proteins / drug effects
  • Recombinant Proteins / metabolism
  • Spiperone / pharmacology
  • Transfection
  • Tritium

Substances

  • Benzopyrans
  • DRD3 protein, human
  • Dopamine Antagonists
  • Pyrroles
  • Receptors, Dopamine D2
  • Receptors, Dopamine D3
  • Recombinant Proteins
  • S 33084
  • Tritium
  • Spiperone