Isovanillin-derived bis-hydrazones as dual cholinesterase and carbonic anhydrase inhibitors: synthesis, enzymatic profiling, and computational insights from molecular docking and dynamics.
The aim is to assess the potential of isovanillin-derived bis-hydrazones as inhibitors for cholinesterase and carbonic anhydrase.
Synthesis of isovanillin-derived bis-hydrazones
Enzymatic profiling to evaluate inhibitory effects
Molecular docking to assess binding interactions
Molecular dynamics simulations to study stability
Compounds 4d, 4a, and 4j demonstrated significant inhibitory activity.
The binding interactions showed strong affinity for both cholinesterase and carbonic anhydrase.
Molecular dynamics indicated stability of the compound-enzyme complexes.
Abstract
Isovanillin-based bis-hydrazones, particularly 4d, 4a, and 4j, represent promising multitarget leads for cholinergic and hCA-linked disorders.
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Isovanillin-derived bis-hydrazones as dual cholinesterase and carbonic anhydrase inhibitors: synthesis, enzymatic profiling, and computational insights from molecular docking and dynamics. | Synapse