Synthesis and biological evaluation of 3,7-diazabicyclo[4.3.0]nonan-8-ones as potential nootropic and analgesic drugs

J Med Chem. 2011 Apr 14;54(7):2512-6. doi: 10.1021/jm101376k. Epub 2011 Mar 7.

Abstract

A series of cis and trans 3,7-diazabicyclo[4.3.0]nonan-8-ones has been synthesized and tested for their ability to revert scopolamine-induced amnesia in the mouse passive-avoidance test. The racemates of the most potent compounds 4 and 7 were separated and tested, but no enantioselectivity was found for the nootropic activity. Compounds 4 and 7 and their enantiomers displayed interesting antihyperalgesic activity in two models of neuropathic pain (streptozotocin-induced and oxalilplatin-induced neuropathy) in comparison with pregabalin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amnesia / chemically induced
  • Amnesia / drug therapy
  • Analgesics / chemical synthesis*
  • Analgesics / chemistry
  • Analgesics / pharmacology*
  • Analgesics / therapeutic use
  • Animals
  • Behavior, Animal / drug effects
  • Drug Design
  • Ketones / chemical synthesis*
  • Ketones / chemistry
  • Ketones / pharmacology*
  • Ketones / therapeutic use
  • Mice
  • Nootropic Agents / chemical synthesis*
  • Nootropic Agents / chemistry
  • Nootropic Agents / pharmacology*
  • Nootropic Agents / therapeutic use
  • Scopolamine / pharmacology
  • Stereoisomerism

Substances

  • Analgesics
  • Ketones
  • Nootropic Agents
  • Scopolamine