Synthesis and discovery of novel hexacyclic cage compounds as inhibitors of acetylcholinesterase

Bioorg Med Chem Lett. 2011 Jul 1;21(13):3997-4000. doi: 10.1016/j.bmcl.2011.05.003. Epub 2011 May 8.

Abstract

Hexacyclic derivatives share vital pharmacological properties, considered useful in Alzheimer's disease. The aim of this study was synthesis and its evaluation for acetyl cholinesterase inhibitory activity of novel hexacyclic analogues. Compound 4f, showed potent inhibitory activity against acetyl cholinesterase enzyme with IC(50) 0.72 μmol/L.

MeSH terms

  • Acetylcholinesterase / chemistry
  • Cholinesterase Inhibitors / chemical synthesis*
  • Cholinesterase Inhibitors / chemistry
  • Cholinesterase Inhibitors / pharmacology
  • Drug Discovery*
  • Heterocyclic Compounds, 4 or More Rings / chemical synthesis*
  • Heterocyclic Compounds, 4 or More Rings / chemistry
  • Heterocyclic Compounds, 4 or More Rings / pharmacology
  • Humans
  • Inhibitory Concentration 50
  • Molecular Structure

Substances

  • Cholinesterase Inhibitors
  • Heterocyclic Compounds, 4 or More Rings
  • Acetylcholinesterase