Discovery of Potent and Selective Blockers Targeting the Epilepsy-Associated KNa1.1 Channel
Gain-of-function (GOF) mutations of the sodium-activated potassium channel KNa1.1 (Slack, Slo2.2, or KCa4.1) induce severe, drug-resistant forms of epilepsy in infants and children. Although quinidine has shown promise in treating KCNT1-related epilepsies compared to other drugs, its limited efficac...
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Veröffentlicht in: | Journal of medicinal chemistry 2024-11, Vol.67 (21), p.19519-19545 |
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Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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