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Multitarget-Directed Ligands Combining Cholinesterase and Monoamine Oxidase Inhibition with Histamine H3 R Antagonism for Neurodegenerative Diseases.

Óscar M Bautista-AguileraStefanie HagenowAlejandra Palomino-AntolinVíctor Farré-AlinsLhassane IsmailiPierre-Louis JoffrinM Luisa JimenoOndrej SoukupJana JanočkováLena KalinowskyEwgenij ProschakIsabel IriepaIgnacio MoraledaJohannes S SchwedAlejandro Romero MartínezFrancisco López-MuñozMourad ChiouaJavier EgeaRona R RamsayJosé Marco-ContellesHolger Stark
Published in: Angewandte Chemie (International ed. in English) (2017)
The therapy of complex neurodegenerative diseases requires the development of multitarget-directed drugs (MTDs). Novel indole derivatives with inhibitory activity towards acetyl/butyrylcholinesterases and monoamine oxidases A/B as well as the histamine H3 receptor (H3R) were obtained by optimization of the neuroprotectant ASS234 by incorporating generally accepted H3R pharmacophore motifs. These small-molecule hits demonstrated balanced activities at the targets, mostly in the nanomolar concentration range. Additional in vitro studies showed antioxidative neuroprotective effects as well as the ability to penetrate the blood-brain barrier. With this promising in vitro profile, contilisant (at 1 mg kg-1 i.p.) also significantly improved lipopolysaccharide-induced cognitive deficits.
Keyphrases
  • lipopolysaccharide induced
  • small molecule
  • inflammatory response
  • protein protein
  • molecular dynamics
  • molecular docking
  • anti inflammatory
  • stem cells
  • binding protein
  • cell therapy