Petrou_2025_Int.J.Mol.Sci_26_

Nineteen previously and newly synthesized amphoteric 8-[(dialkylamino)methyl]-7-hydroxy-4-(2-oxo-2H-chromen-3-yl)-2H-chromen-2-ones were assayed as inhibitors of monoamine oxidases (MAO-A and B) and cholinesterases (AChE and BChE). Five of the tested compounds (2b, 2c, 3c, 5b, and 5c), namely those bearing the less bulky alkyls in the Mannich base 8-CH(2)NR(2) (R = Me, Et) and the halogens (Cl, Br) at C6 of the 4-coumarin-3-yl moiety, showed moderate inhibitory potencies toward human MAO-A in the single-digit micromolar range (IC(50)s from 1.49 to 3.04 microM). In particular, the 6'-Cl derivatives 2b and 5b proved to be reversible competitive inhibitors of human MAO-A with K(i) values of 0.272 and 0.326 microM. Among the tested compounds, 3c proved to also be a moderate inhibitor of human AChE (IC(50) 4.27 microM). Molecular docking calculations suggested binding modes of the most active compounds to MAO-A and AChE binding sites consistent enough with the experimental data. Chemoinformatic tools suggest for the most active compounds, including the dual MAO-A/AChE inhibitor 3c, full compliance with Lipinski's rule of five, high probability of gastrointestinal absorption, but low blood-brain barrier (BBB) permeability. While further efforts are required to improve their CNS distribution, herein new phenolic Mannich bases have been identified that may have potential for treating neurodegenerative syndromes.