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Design, Synthesis, and Evaluation of Novel Quinazolin‐4(3 H )‐One Derivatives: Anti‐Leishmanial Activity, Selectivity, and Molecular Docking Insights

Year: 2025

Type: article

Abstract: ABSTRACT In this study, 16 novel quinazolin‐4(3 H )‐one derivatives were synthesized and evaluated for their antileishmanial activity against Leishmania major and Leishmania donovani . Among them, compounds 2 (4‐hydroxy substituted) and 9 (4‐morpholino substituted) exhibited the highest efficacy, with compound 2 showing IC 50 values of 23.94 μM for L. major and 90.80 μM for L. donovani , while compound 9 demonstrated IC 50 values of 23.05 μM for L. major and 56.30 μM for L. donovani . Miltefosine, the reference drug, showed IC 50 values of 32.89 μM for L. major , 4.78 μM for L. donovani , and 7.53 μM for HUVEC cells. Compound 2 showed superior selectivity (SI = 15.2 for L. major and 4.0 for L. donovani ) compared to miltefosine (SI = 4.4 for L. major and 0.6 for L. donovani ). Molecular docking studies identified phosphodiesterase B1 (PDEB1) as a key target, with compound 2 showing the strongest binding affinity. The docking score of compound 2 was calculated as –11.909 kcal/mol for PDEB1. ADME predictions indicated compound 2 's favorable pharmacokinetic profile, including good solubility, permeability, and adherence to Lipinski's Rule of Five. Overall, compound 2 exhibited the most promising therapeutic profile, highlighting its potential as a lead compound for antileishmanial drug development.

Source: Journal of Biochemical and Molecular Toxicology

DOI: 10.1002/jbt.70309

Authors: Baycan Mor, Feyzi Sinan Tokalı, Barış Yıldız, Halil Şenol, Şeyma Aksu, Neriman Mor

Institutions: Kafkas University, Bezmiâlem Vakıf Üniversitesi

Language: English

Topic: Quinazolinone synthesis and applications

Subfield: Organic Chemistry

Field: Chemistry

Domain: Physical Sciences

SDG: Good health and well-being

Open Access status: bronze

Funder: Kafkas Üniversitesi