Evaluation of the antiprion activity of 6-aminophenanthridines and related heterocycles

Eur J Med Chem. 2014 Jul 23:82:363-71. doi: 10.1016/j.ejmech.2014.05.083. Epub 2014 Jun 3.

Abstract

Series of 6-aminophenanthridines and related heterocyclic compounds such as benzonaphtyridines were prepared. Reduction of one of the three aromatic rings was also performed. The compounds were first tested for their antiprion activity in a previously described yeast-based colourimetric prion assay. The most potent derivatives were then assayed ex vivo against the mammalian prion PrP(Sc) in a cell-based assay. Several of the new compounds were found more potent than the parent lead 6-aminophenanthridine. The most promising compounds against yeast and mammalian prions were 8-azido-6-aminophenanthridine (3m), and 7,10-dihydrophenanthridin-6-amine (14). In the mammalian cell-based assay, the IC50 of these two compounds were around 5 μM and 1.8 μM, respectively.

Keywords: Neurodegenerative diseases; Phenanthridine; Prions; Protein misfolding.

MeSH terms

  • Animals
  • Heterocyclic Compounds / chemical synthesis
  • Heterocyclic Compounds / chemistry
  • Heterocyclic Compounds / pharmacology*
  • Mice
  • Mice, Transgenic
  • Models, Molecular
  • Molecular Structure
  • Phenanthridines / chemical synthesis
  • Phenanthridines / chemistry
  • Phenanthridines / pharmacology*
  • Prions / antagonists & inhibitors*
  • Prions / metabolism
  • Saccharomyces cerevisiae / chemistry
  • Saccharomyces cerevisiae / metabolism
  • Structure-Activity Relationship

Substances

  • 6-aminophenanthridine
  • Heterocyclic Compounds
  • Phenanthridines
  • Prions