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In 2024, Kalaimathi and colleagues conducted an in silico analysis in which amygdalin, along with other phytochemicals such as eriocitrin, keracyanin, and amaroswerin, was identified as a potential natural inhibitor of BACE1

The high affinity of UCB for neuronal membranes causes a conformational change in the NMDA receptor, resulting in an open and activated NMDA receptor-ion channel complex [19]