3-(4-Piperidinylalkyl)indoles, selective inhibitors of neuronal 5-hydroxytryptamine uptake

J Med Chem. 1980 Dec;23(12):1306-10. doi: 10.1021/jm00186a005.

Abstract

A series of 3-(4-piperidinylalkyl)indoles was synthesized and tested as uptake inhibitors of biogenic amines. Some of these compounds are potent and very selective in blocking the 5-hydroxytryptamine (5-HT) uptake, as evidenced by biochemical data and behavioral tests. A discussion on structure-activity relationships is given. The most interesting member of the series, indalpine, 3-[2-(4-piperidinyl)ethyl]indole (1), was selected for clinical studies.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Blood Platelets / metabolism
  • Chemical Phenomena
  • Chemistry
  • Humans
  • In Vitro Techniques
  • Indoles / chemical synthesis*
  • Indoles / pharmacology
  • Mice
  • Neurons / drug effects
  • Neurons / metabolism*
  • Rats
  • Serotonin Antagonists / chemical synthesis*
  • Structure-Activity Relationship
  • Synaptosomes / metabolism

Substances

  • Indoles
  • Serotonin Antagonists