Novel ligands rationally designed for characterizing I2-imidazoline binding sites nature and functions

J Med Chem. 2008 Aug 28;51(16):5130-4. doi: 10.1021/jm800400k. Epub 2008 Jul 29.

Abstract

The study of two series of 2-aryl-ethylen-imidazolines 3-7 and 8-12 inspired by I2-IBS ligands phenyzoline (1) and diphenyzoline (2), respectively, confirmed the interesting "positive" or "negative" morphine analgesia modulation displayed by their corresponding leads and demonstrated that these effects might be correlated with morphine tolerance and dependence, respectively. By comparative examination of rationally designed compounds, some analogies between binding site cavity of I2-IBS proteins and alpha 2C-adrenoreceptor emerged.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics / pharmacology
  • Animals
  • Drug Design
  • Imidazoles / chemical synthesis
  • Imidazoles / metabolism*
  • Imidazoline Receptors / chemistry*
  • Imidazoline Receptors / physiology*
  • Imidazolines / chemistry*
  • Imidazolines / pharmacology
  • Ligands
  • Mice
  • Morphine / pharmacology
  • Pain / drug therapy
  • Rats
  • Receptors, Adrenergic, alpha-2 / drug effects

Substances

  • Analgesics
  • Imidazoles
  • Imidazoline Receptors
  • Imidazolines
  • Ligands
  • Receptors, Adrenergic, alpha-2
  • Morphine