Discovery of new acetylcholinesterase inhibitors derived from quinazolinones: synthesis, in vitro, and molecular docking study

In the present study, twelve quinazolinones ( 2, 3, 4a–4j ) were successfully synthesized. Among them, five compounds ( 4c, 4d, 4f, 4h, 4i ) were newly reported. Furthermore, twelve compounds were assessed against acetylcholinesterase (AChE). Seven compounds ( 4b, 4c, 4d, 4f, 4g, 4h, 4j ) showed inhibitory activity above 70%, where compounds 4c and 4h had inhibitory activity with IC₅₀ values of 2.97 and 5.86 μM, respectively. The kinetic study showed that compounds 4c and 4h exhibited mixed-type inhibition. Molecular docking suggested that compounds 4c and 4h displayed binding energy values of −8.7 and −8.4 kcal/mol. Compound 4c showed H-bonds with four residues (Tyr124, Tyr337, Tyr341, and Glu202), but compound 4h formed H-bonds with three residues (Tyr124, Tyr133, and Glu202) in the binding pocket of AChE. Thus, quinazolinone derivatives with a nitro group at the C-6 and alkoxy groups at the C-7 position have the potential for further investigation as AChE inhibitors.

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Publication Details

Journal
Pharmacia
Published
2025-10-15
DOI
https://doi.org/10.3897/pharmacia.72.e162676
Primary Topic
Cholinesterase and Neurodegenerative Diseases
Type
article
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article

Discovery of new acetylcholinesterase inhibitors derived from quinazolinones: synthesis, in vitro, and molecular docking study

Didin Mujahidin, Iqbal Musthapa, Ade Danova, Robby Roswanda et al.
Pharmacia
Cholinesterase and Neurodegenerative Diseases
article

Discovery of new acetylcholinesterase inhibitors derived from quinazolinones: synthesis, in vitro, and molecular docking study

Didin Mujahidin, Iqbal Musthapa, Ade Danova, Robby Roswanda, Fera Kurniadewi, Warinthorn Chavasiri, A. Christy, Elvira Hermawati
article en

Abstract

In the present study, twelve quinazolinones ( 2, 3, 4a–4j ) were successfully synthesized. Among them, five compounds ( 4c, 4d, 4f, 4h, 4i ) were newly reported. Furthermore, twelve compounds were assessed against acetylcholinesterase (AChE). Seven compounds ( 4b, 4c, 4d, 4f, 4g, 4h, 4j ) showed inhibitory activity above 70%, where compounds 4c and 4h had inhibitory activity with IC₅₀ values of 2.97 and 5.86 μM, respectively. The kinetic study showed that compounds 4c and 4h exhibited mixed-type inhibition. Molecular docking suggested that compounds 4c and 4h displayed binding energy values of −8.7 and −8.4 kcal/mol. Compound 4c showed H-bonds with four residues (Tyr124, Tyr337, Tyr341, and Glu202), but compound 4h formed H-bonds with three residues (Tyr124, Tyr133, and Glu202) in the binding pocket of AChE. Thus, quinazolinone derivatives with a nitro group at the C-6 and alkoxy groups at the C-7 position have the potential for further investigation as AChE inhibitors.

PharmaciaVol. 72
Indonesia University of Education (ID), Bandung Institute of Technology (ID), Chulalongkorn University (TH), State University of Jakarta (ID)
Openalex Percentile: Top 67%
Cholinesterase and Neurodegenerative Diseases
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