QNZ46 is a highly selective noncompetitive NMDA receptor antagonist targeting GluN2C/D ( IC 50 =3.9 μM), GluN1/GluN2C ( IC 50 =7.1 μM), and GluN1/GluN2D ( IC 50 =182 μM) subunits. QNZ46 inhibits glutamate-mediated calcium influx, thereby blocking excitotoxicity. QNZ46 is membrane permeable and can cross the blood-brain barrier, where it inhibits myelin damage and axonal degeneration.
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