Rational design, synthesis, biologic evaluation, and structure-activity relationship studies of novel 1-indanone alpha(1)-adrenoceptor antagonists

Chem Biol Drug Des. 2007 Nov;70(5):461-4. doi: 10.1111/j.1747-0285.2007.00581.x. Epub 2007 Oct 10.

Abstract

In the present report, a novel series of 1-indanone alpha(1)-adrenoceptor antagonists were designed and synthesized based on 3D-pharmacophore model. Their in vitro alpha(1)-adrenoceptor antagonistic assay showed that three compounds (2a, 2m, and 2o) had similar or improved alpha(1)-adrenoceptor antagonistic activities relative to the positive control prazosin. Based on these results, a three-dimensional quantitative structure-activity relationship study was performed using a Self-Organizing Molecular Field Analysis method to provide insight for the future development of alpha(1)-adrenoceptor antagonists.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenergic alpha-Antagonists / chemical synthesis*
  • Adrenergic alpha-Antagonists / pharmacology*
  • Drug Design
  • Indans / chemical synthesis*
  • Indans / pharmacology*
  • Models, Molecular
  • Molecular Conformation
  • Prazosin / pharmacology
  • Receptors, Adrenergic / drug effects*
  • Structure-Activity Relationship

Substances

  • Adrenergic alpha-Antagonists
  • Indans
  • Receptors, Adrenergic
  • Prazosin