Publication | Open Access

Design, synthesis, biological evaluation and docking study of 4-isochromanone hybrids bearing N-benzyl pyridinium moiety as dual binding site acetylcholinesterase inhibitors

Combinatorial ChemistryMedicinal ChemistryBiochemistryNatural SciencesMedicine4-Isochromanone HybridsOrganic ChemistryBiological EvaluationHeterocycle ChemistryN-benzyl Pyridinium MoietyPharmacologySynthetic ChemistryDrug Discovery