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Computational docking simulation indicated that Van der Waals interactions between zerumbone and both the cholinesterases had been the key forces responsible for its inhibitory effects. Additionally, zerumbone showed top physicochemical properties both for bioavailability and blood-brain barrier (Better Business Bureau) permeability. Together, in our research, zerumbone had been obviously identified as a unique twin AChE and BChE inhibitor with high permeability

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