Selective and enantiospecific acylation of kappa opioid receptors by (1S,2S)-trans-2-isothiocyanato-N-methyl-N-[2-(1-pyrrolidinyl) cyclohexy l] benzeneacetamide. Demonstration of kappa receptor heterogeneity

J Med Chem. 1989 Feb;32(2):281-3. doi: 10.1021/jm00122a001.
No abstract available

MeSH terms

  • Acylation
  • Animals
  • Benzeneacetamides*
  • Benzomorphans / metabolism
  • Cyclohexanes / pharmacology*
  • Guinea Pigs
  • In Vitro Techniques
  • Pyrrolidines / metabolism
  • Pyrrolidines / pharmacology*
  • Receptors, Opioid / metabolism*
  • Receptors, Opioid, kappa
  • Stereoisomerism

Substances

  • Benzeneacetamides
  • Benzomorphans
  • Cyclohexanes
  • Pyrrolidines
  • Receptors, Opioid
  • Receptors, Opioid, kappa
  • 2-isothiocyanato-N-methyl-N-(2-(1-pyrrolidinyl)cyclohexyl)benzeneacetamide
  • bremazocine
  • U 69593