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Pyrazolines as potential anti-Alzheimer's agents: DFT, molecular docking, enzyme inhibition and pharmacokinetic studies.

Valkiria MachadoArthur Ribeiro CenciKerolain F TeixeiraLarissa SensTiago TizzianiRicardo J NunesLeonardo L G FerreiraRosendo A YunesLouis P SandjoAdriano D AndricopuloAldo Sena de Oliveira
Published in: RSC medicinal chemistry (2022)
Alzheimer's disease (AD) is a neurodegenerative disease that is characterized as the main dementia in the elderly. Eighteen pyrazolines were synthesized and evaluated for their inhibitory effects against acetylcholinesterase (AChE) in vitro . Possible interactions between pyrazolines and the enzyme were explored by in silico experiments. Compound 2B of the series was the most active pyrazoline with an IC 50 value of 58 nM. Molecular docking studies revealed two important π-π interactions with residues Trp 286 and Tyr 341. A correlation between the HOMO-1 surface and AChE inhibition was observed. ADMET assays demonstrated a good profile for compound 2B. From the abovementioned findings, a new avenue of compound 2B analogues could be explored to develop anti-AD agents.
Keyphrases
  • molecular docking
  • molecular dynamics simulations
  • cognitive decline
  • mild cognitive impairment
  • case control
  • cognitive impairment
  • community dwelling