Synthesis and evaluation of clioquinol-rolipram/roflumilast hybrids as multitarget-directed ligands for the treatment of Alzheimer's disease

Eur J Med Chem. 2019 Feb 1:163:512-526. doi: 10.1016/j.ejmech.2018.12.013. Epub 2018 Dec 7.

Abstract

Considering the importance of PDE4D inhibition and the modulation of biometals in Alzheimer's disease (AD) therapeutics, we have designed, synthesized and evaluated a series of new clioquinol-rolipram/roflumilast hybrids as multitarget-directed ligands for the treatment of AD. In vitro studies demonstrated that some of the molecules processed remarkable inhibitory activity against phosphodiesterase 4D (PDE4D), strong intracellular antioxidant capacity, potent inhibition of metal-induced aggregation of Aβ, and potential blood-brain barrier permeability. Compound 7a demonstrated significant improvement in cognitive and spatial memory in an Aβ25-35-induce mouse model in Morris water-maze test (MWM). These results indicate that compound 7a is a promising multifunctional candidate that is worthy of further study.

Keywords: Alzheimer's disease; Metal chelating agents; Multitarget-directed ligands; PDE4D inhibitors.

MeSH terms

  • Alzheimer Disease / drug therapy*
  • Aminopyridines / chemical synthesis
  • Aminopyridines / pharmacology*
  • Animals
  • Benzamides / chemical synthesis
  • Benzamides / pharmacology*
  • Clioquinol / chemical synthesis
  • Clioquinol / pharmacology*
  • Cyclic Nucleotide Phosphodiesterases, Type 4 / drug effects*
  • Cyclopropanes / chemical synthesis
  • Cyclopropanes / pharmacology
  • Drug Design*
  • Humans
  • Ligands
  • Mice
  • Rats
  • Rolipram / chemical synthesis
  • Rolipram / pharmacology*

Substances

  • Aminopyridines
  • Benzamides
  • Cyclopropanes
  • Ligands
  • Roflumilast
  • Clioquinol
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • PDE4D protein, human
  • Rolipram