فهرست نشریات علمی دسترسی آزاد ایران

A series of novel acridine-based aminoacetamide derivatives (AN1, AN8, BI7, AAM3, and AC1) were synthesized and structurally confirmed using FTIR, NMR, and LC–MS techniques. This study aimed to evaluate the compounds as potential acetylcholinesterase (AChE) inhibitors with anticancer activity. Molecular docking was performed using the AChE crystal structure (PDB ID: 4EY6) to predict ligand–enzyme interactions. All derivatives showed favorable binding affinities (–8.0 to –8.3 kcal/mol), indicating strong compatibility with the catalytic pocket. AC1 demonstrated the highest affinity (–8.3 kcal/mol), supported by hydrogen bonds with Gly437 and Arg434 and π–π stacking with Trp441 and Trp754, while AN1 and AN8 exhibited stable poses through π–cation and hydrogen bonding interactions. The cytotoxic potential of the derivatives was assessed against SH-SY5Y neuroblastoma cells using the MTT assay. AC1 displayed the strongest antiproliferative effect (IC₅₀ = 26.92 ± 0.57 μg/mL), surpassing the standard reference compound (IC₅₀ = 92.67 ± 0.43 μg/mL). AN1 (IC₅₀ = 47.74 ± 0.98 μg/mL) and AN8 (IC₅₀ = 69.95 ± 0.49 μg/mL) showed moderate cytotoxicity, while BI7 and AAM3 were considerably less active (IC₅₀ values > 277 μg/mL). A clear correlation was observed between docking affinity and experimental cytotoxicity, particularly for AC1 and AN1. Overall, AC1 emerged as the most promising derivative, highlighting the impact of structural modifications on anticancer activity. The combined computational and in vitro results support acridine-based aminoacetamide scaffolds as potential leads for anticancer drug development.