# Structural and Mechanistic Insights into Dual Cholinesterase Inhibition by Marine Phytohormones

## TL;DR

This study explores marine phytohormones as potential treatments for Alzheimer's by inhibiting enzymes that break down acetylcholine, a key brain chemical.

## Contribution

The study reveals the dual and distinct cholinesterase inhibition mechanisms of marine phytohormones, supported by computational and experimental evidence.

## Key findings

- Isopentenyl adenine (IPA) inhibits both AChE and BChE through noncompetitive and competitive mechanisms, respectively.
- Abscisic acid (ABA) selectively inhibits AChE in a noncompetitive manner.
- Both compounds show favorable ADMET profiles and low off-target effects.

## Abstract

Cholinergic dysfunction is a hallmark of Alzheimer’s disease (AD), driven by elevated acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) activity that depletes acetylcholine and contributes to amyloid pathology. Current AD treatments face major challenges, including poor brain penetration, short effect duration and safety concerns, highlighting the need for compounds suitable for preventive or earlier-stage intervention. This study investigated marine phytohormones as modulators of cholinergic imbalance, using an integrative strategy encompassing enzymatic assays, QSAR and DFT calculations, molecular docking, molecular dynamics (MD) simulations, and ADMET profiling. Among them, isopentenyl adenine (IPA) and abscisic acid (ABA) showed inhibitory activity against cholinesterases. IPA inhibited both AChE and BChE through distinct mechanisms with noncompetitive inhibition of AChE and competitive inhibition of BChE, while ABA showed selective noncompetitive inhibition of AChE. DFT-based analysis revealed distinct electronic properties supporting differential reactivity. Moreover, IPA interacted with both catalytic and peripheral residues in AChE, and aligned with BChE’s active site, while ABA was bound more peripherally. MD simulations confirmed complex-specific conformational stability based on RMSD, RMSF, Rg, and hydrogen bonding analysis. Both compounds showed low off-target potential against serine proteases and favorable predicted ADMET profiles. These results support the potential of marine phytohormones as preventive modulators of cholinergic dysfunction in AD.