Structural determinants of selective affinity for brain D-1 dopamine receptors within a series of 1-phenyl-1H-3-benzazepine analogues of SK&F 38393 and SCH 23390

This publication has 11 references indexed in Scilit:

• Sniffing, rearing and locomotor responses to the D-1 dopamine agonist R-SK&F 38393 and to apomorphine: Differential interactions with the selective D-1 and D-2 antagonists SCH 23390 and metoclopramide
  European Journal of Pharmacology, 1985
• Identification of the enantiomers of SK&F 83566 as specific and stereoselective antagonists at the striatal D-1 dopamine receptor: Comparisons with the D-2 enantioselectivity of Ro 22-1319
  European Journal of Pharmacology, 1984
• The chemical basis for the blockade of the D-1 dopamine receptor by SCH 23390
  European Journal of Pharmacology, 1984
• Pharmacological effects of a specific dopamine D-1 antagonist SCH 23390 in comparison with neuroleptics
  Life Sciences, 1984
• Selective and stereospecific interactions of R-SK&F 38393 with [3H]piflutixol but not [3H]spiperone binding to striatal D1 and D2 dopamine receptors: Comparisons with SCH 23390
  European Journal of Pharmacology, 1984
• Dopaminergic behaviour stereospecifically promoted by the D1 agonist R-SK & F 38393 and selectively blocked by the D1 antagonist SCH 23390
  Psychopharmacology, 1984
• Preferential inhibition of ligand binding to calf striatal dopamine D1 receptors by SCH 23390
  Neuropharmacology, 1983
• SCH 23390—The first selective dopamine D-1 antagonist
  European Journal of Pharmacology, 1983
• Absolute stereochemistry and dopaminergic activity of enantiomers of 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
  Journal of Medicinal Chemistry, 1982
• The central effects of a novel dopamine agonist
  European Journal of Pharmacology, 1978