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February 12, 2026Journal of Chemometrics2 citations

Multifactorial 1, 3, 4‐Oxadiazole Derivatives as Cholinesterase and Glycogen Synthase Kinase‐3 β Inhibitors for Targeting Alzheimer's Disease: QSAR‐Based Virtual Screening, MD Docking, Free Energy Analysis, ADMET, and DFT Studies

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NCNikita ChhabraBMBalaji Wamanrao MatoreAMAnjali Murmu

Key Points

  • The study aims to design and identify multitarget cholinesterase and GSK3β inhibitors for Alzheimer's disease treatment using computational methods.
  • Developed QSAR models using GA-MLR from a dataset of 273 compounds.
  • Conducted virtual screening of 3404 1,3,4-oxadiazoles to identify promising candidates.
  • Performed molecular dynamics docking and binding energy calculations.
  • Evaluated ADMET properties for pharmacokinetics and toxicity.
  • Utilized DFT analysis for reactivity assessment.
  • Identified 72 potential hits with IC₅₀ ≤ 300 nM.
  • Compound 2851 showed superior binding energies compared to donepezil.
  • ADMET analysis indicated favorable profiles for compound 2851.
  • DFT revealed enhanced reactivity and lower band gaps for compound 2851.

Abstract

ABSTRACT Alzheimer's disease (AD) involves multiple pathogenic pathways, yet current therapeutic strategies remain largely symptomatic and focused on single molecular targets, underscoring a critical existing gap, emphasizing the need for rational multitarget drug design. Addressing this limitation, the present study employed an integrated in silico framework to identify multitarget 1,3,4‐oxadiazole derivatives against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and glycogen synthase kinase‐3 β (GSK3β). A dataset of 273 reported compounds was used to develop robust QSAR models via Genetic Algorithm‐Multiple Linear Regression (GA‐MLR), exhibiting strong internal ( R 2 = 0.638–0.758, Q 2 LOO = 0.609–0.736) and satisfactory external predictivity ( Q 2 F1 − Q 2 F2 = 0.566–0.800). Subsequent virtual screening of 3404 1,3,4‐oxadiazoles from BindingDB identified 72 promising hits (IC₅₀ ≤ 300 nM), which underwent molecular dynamics (MD) docking. MD‐based CDOCKER analysis highlighted compound 2851 with superior binding energies and stable key interactions compared to donepezil, supported by binding free energy (Δ G ) calculations. ADMET evaluation indicated favorable pharmacokinetic and toxicity profiles, while density functional theory (DFT) analysis revealed enhanced reactivity and lower band gaps. This integrated computational workflow identified compound 2851 as a promising MT therapeutic agent for AD.

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Cite This Study

Chhabra et al. (2026) studied this question.

synapsesocial.com/papers/698d6d795be6419ac0d52689https://doi.org/10.1002/cem.70107
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