Synthesis, antiproliferative activity, ADMET, molecular docking, molecular dynamics simulation, and DFT study for coumarin-based 1,5-benzothiazepines

Abstract

Some α,β-unsaturated ketones 5a–h were prepared from 3-acetyl-4-hydroxycoumarin and (hetero)aromatic aldehydes with yields of 58–62%. These ketones were converted into novel coumarin–benzothiazepine hybrid compounds 6a–h by their reaction with o-aminothiophenol in the presence of glacial acetic acid as the catalyst with yields of 62–82%. All the synthesized compounds 6a–h were screened for their in vitro anticancer activity against human squamous cell carcinoma KB and hepatocellular carcinoma HepG2 cancer lines. Compound 6h exhibited the most potent inhibitory activity in this series, with the corresponding IC₅₀ values of 4.0 and 6.25 μM for KB and HepG2 cell lines. The cytotoxicity assay on WI-38 cells showed that the most active compounds, 6b, 6d, 6f, and 6h, had the low cytotoxicity, and of these compounds, compound 6h exhibited the lowest toxicity. ADMET properties indicated that compound 6h had drug-like behaviour. The molecular docking results for the most active compounds 6b, 6d, 6f, and 6h indicated the active interactions between each ligand and the residues in the binding pocket of enzyme 1Z5M. The molecular (MD) dynamics simulation applied for compound 6h showed the interactions of this ligand with residues LEU88, ALA109, GLU166, LYS111, and LEU212 in the active pocket of 1Z5M during 200 ns MD simulations. Furthermore, the electronic characteristics of the most active compounds 6b, 6d, 6f, and 6h were investigated by using a density functional theory (DFT) method at the B3LYP/6-311++G(d,p) basis level. The frontier molecular orbital (FMO) energy and atomic net charges were examined.