Development of novel pain relief agents acting through the selective activation of the delta-opioid receptor

Farmaco. 2000 Mar;55(3):178-80. doi: 10.1016/s0014-827x(00)00015-x.

Abstract

A continuing effort in the development of non-peptide delta-opioid agonists as possible safe and effective pain relief agents has been seen in the last years. Novel potent and selective delta-opioid agonists based on the pirrolomorphinan framework have been designed, synthesised and biologically characterised in our laboratories. In particular, compound 7 (SB 235863) proved the concept that a selective delta-opioid agonist may be a valuable pain relief agent free of the unwanted side-effects usually associated with narcotic analgesics such as morphine.

MeSH terms

  • Analgesics, Opioid / chemical synthesis*
  • Analgesics, Opioid / pharmacokinetics
  • Analgesics, Opioid / pharmacology
  • Animals
  • Brain / metabolism
  • Cell Line
  • Models, Molecular
  • Rats
  • Receptors, Opioid, delta / drug effects*
  • Structure-Activity Relationship

Substances

  • Analgesics, Opioid
  • Receptors, Opioid, delta