Relutrigine (PRAX-562) is an orally active inhibitor of persistent sodium channel . Relutrigine potently and preferentially inhibits persistent I Na induced by ATX-II (Nav 1.5 activator) or the SCN8A mutation N1768D with IC 50 values of 141 nM and 75 nM, respectively. Relutrigine exhibits potent use-dependent block and reduces neuronal intrinsic excitability. Relutrigine has effective anticonvulsant activity.
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