Adamantane and protoadamantanealkanamines as potential anti-Parkinson agents

J Med Chem. 1976 Jul;19(7):967-9. doi: 10.1021/jm00229a022.

Abstract

The synthesis of 2-halo-1-adamantanemethanamines, 4-protoadamantanemethanamines, and 4-protoadamantaneamines is described. The anti-Parkinson activity of these amines in terms of reversal of reserpine-induced catalepsy in rats has been evaluated and compared with amantadine. 2-Bromo- and 2-chloro-1-adamantanemethanamines are shown to be twice as active as amantadine.

MeSH terms

  • Adamantane / analogs & derivatives
  • Adamantane / chemical synthesis*
  • Adamantane / pharmacology
  • Adamantane / toxicity
  • Amines / chemical synthesis
  • Amines / pharmacology
  • Amines / toxicity
  • Animals
  • Antiparkinson Agents / chemical synthesis*
  • Antiparkinson Agents / toxicity
  • Body Temperature / drug effects
  • Bridged-Ring Compounds / chemical synthesis*
  • Lethal Dose 50
  • Mice
  • Motor Activity / drug effects
  • Rats
  • Reserpine / antagonists & inhibitors

Substances

  • Amines
  • Antiparkinson Agents
  • Bridged-Ring Compounds
  • Reserpine
  • Adamantane