Structure-activity relationship study of tryptophan-based butyrylcholinesterase inhibitors

Eur J Med Chem. 2020 Dec 15:208:112766. doi: 10.1016/j.ejmech.2020.112766. Epub 2020 Aug 22.

Abstract

A series of tryptophan-based selective nanomolar butyrylcholinesterase (BChE) inhibitors was designed and synthesized. Compounds were optimized in terms of potency, selectivity, and synthetic accessibility. The crystal structure of the inhibitor 18 in complex with BChE revealed the molecular basis for its low nanomolar inhibition (IC50 = 2.8 nM). The favourable in vitro results enabled a first-in-animal in vivo efficacy and safety trial, which demonstrated a positive impact on fear-motivated and spatial long-term memory retrieval without any concomitant adverse motor effects. Altogether, this research culminated in a handful of new lead compounds with promising potential for symptomatic treatment of patients with Alzheimer's disease.

Keywords: Alzheimer’s disease; Butyrylcholinesterase; Cholinesterase inhibitors; Neurodegenerative diseases.

MeSH terms

  • Alzheimer Disease / drug therapy*
  • Animals
  • Butyrylcholinesterase / metabolism*
  • Cholinesterase Inhibitors / chemical synthesis
  • Cholinesterase Inhibitors / therapeutic use*
  • Cholinesterase Inhibitors / toxicity
  • Maze Learning / drug effects
  • Memory / drug effects
  • Mice
  • Molecular Structure
  • Nootropic Agents / chemical synthesis
  • Nootropic Agents / therapeutic use*
  • Nootropic Agents / toxicity
  • Structure-Activity Relationship
  • Tryptophan / analogs & derivatives*
  • Tryptophan / therapeutic use*
  • Tryptophan / toxicity

Substances

  • Cholinesterase Inhibitors
  • Nootropic Agents
  • Tryptophan
  • Butyrylcholinesterase