Synthesis, in vitro binding profile, and central nervous system penetrability of the highly potent 5-HT3 receptor antagonist [3H]-4-(2-methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole

J Med Chem. 1990 Nov;33(11):3020-3. doi: 10.1021/jm00173a017.

Abstract

4-(2-Methoxyphenyl)-2-[4(5)-methyl-5(4)-imidazolylmethyl]thiazole (5) is a highly potent member of a structurally novel series of selective serotonin-3 receptor antagonists. The synthesis of tritiated 5 and its binding profile in neuroblastoma-glioma 108-15 cells are described. Furthermore, in vivo studies in rat with this radioligand indicate that it effectively penetrates the blood-brain barrier upon peripheral administration. Thus, 5 should be a useful pharmacological tool for both in vitro and in vivo studies of this class of compounds.

MeSH terms

  • Animals
  • Blood-Brain Barrier
  • Brain / metabolism*
  • Chemical Phenomena
  • Chemistry
  • Glioma / metabolism
  • Imidazoles / chemical synthesis*
  • Imidazoles / metabolism
  • Imidazoles / pharmacokinetics
  • Mice
  • Molecular Structure
  • Neuroblastoma / metabolism
  • Serotonin Antagonists*
  • Thiazoles / chemical synthesis*
  • Thiazoles / metabolism
  • Thiazoles / pharmacokinetics
  • Tumor Cells, Cultured

Substances

  • Imidazoles
  • Serotonin Antagonists
  • Thiazoles
  • 4-(2-methoxyphenyl)-2-(4(5)-methyl-5(4)-imidazolylmethyl)thiazole