Inhibition of monoamine oxidases by coumarin-3-acyl derivatives: biological activity and computational study

Bioorg Med Chem Lett. 2004 Jul 16;14(14):3697-703. doi: 10.1016/j.bmcl.2004.05.010.

Abstract

A series of coumarin-3-acyl derivatives have been synthesized and investigated for the ability to inhibit selectively monoamine oxidases. The coumarin-3-carboxylic acids, 2a-e, proved to be reversible and selective inhibitors of the MAO-B isoform, displaying pIC(50) values of particular interest: 2a shows pIC(50) 7.76 and a selectivity index (pS.I.) 2.94 and 2b shows pIC(50) 7.72 and a pS.I. of 2.80. The coumarin-3-acyl chlorides 3a-e showed high pIC(50) values against both MAO-A and MAO-B isoforms, 3d being the highest against MAO-B with a pIC(50) value of 8.00. In order to rationalize the activity/selectivity results, molecular descriptors were generated. Further insight about enzyme-inhibitor interaction was obtained by docking experiments with the MAO-B isoform.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amine Oxidase (Copper-Containing) / antagonists & inhibitors
  • Amine Oxidase (Copper-Containing) / metabolism*
  • Animals
  • Binding Sites / drug effects
  • Brain / drug effects
  • Brain / enzymology
  • Cell Line
  • Computational Biology
  • Coumarins / chemical synthesis*
  • Coumarins / chemistry
  • Coumarins / pharmacology
  • Inhibitory Concentration 50
  • Molecular Conformation
  • Monoamine Oxidase Inhibitors / chemical synthesis*
  • Monoamine Oxidase Inhibitors / pharmacology
  • Structure-Activity Relationship

Substances

  • Coumarins
  • Monoamine Oxidase Inhibitors
  • Amine Oxidase (Copper-Containing)
  • coumarin-3-carboxylic acid