Structure-antitussive activity relationships of naltrindole derivatives. Identification of novel and potent antitussive agents

J Med Chem. 2008 Aug 14;51(15):4404-11. doi: 10.1021/jm701440h. Epub 2008 Jul 19.

Abstract

We have previously reported antitussive effects of naltrindole (NTI), a typical delta opioid receptor antagonist, in a rat model. The ED50 values of NTI by intraperitoneal and peroral injections were 104 microg/kg and 1840 microg/kg, respectively, comparable to those of codeine. Codeine, one of the most reliable centrally acting antitussive drugs, has micro agonist activity and thus the same side effects as morphine, e.g., constipation, dependency, and respiratory depression. Because NTI is a delta opioid antagonist, its derivatives have potential as highly potent antitussives, free from the mu opioid agonist side effects. We attempted to optimize the NTI derivatives to develop novel antitussive agents. On the basis of the studies of structure-antitussive activity relationships of alkyl substituted NTI derivatives, we designed NTI derivatives with extra ring fused structures. As a clinical candidate, we identified a highly potent new compound, (5R,9R,13S,14S)-17-cyclopropylmethyl-6,7-didehydro-4,5-epoxy-5',6'-dihydro-3-methoxy-4'H-pyrrolo[3,2,1-ij]quinolino[2',1':6,7]morphinan-14-ol (5b) methanesulfonate (TRK-850) which was effective even by oral administration (ED50 6.40 microg/kg).

MeSH terms

  • Alkylation
  • Animals
  • Antitussive Agents / chemical synthesis*
  • Antitussive Agents / chemistry
  • Antitussive Agents / therapeutic use*
  • CHO Cells
  • Capsaicin / pharmacology
  • Cough / chemically induced
  • Cough / drug therapy
  • Cricetinae
  • Cricetulus
  • Male
  • Mice
  • Molecular Structure
  • Naltrexone / analogs & derivatives*
  • Naltrexone / chemical synthesis
  • Naltrexone / chemistry
  • Naltrexone / therapeutic use
  • Rats
  • Structure-Activity Relationship

Substances

  • Antitussive Agents
  • Naltrexone
  • naltrindole
  • Capsaicin