Benzenesulfonamides act as open-channel blockers on KV3.1 potassium channel | SpringerLink
The external TEA binding site and C-type inactivation in voltage-gated potassium channels. Biophys J 87:3148-3161 ... Ramos E, OLeary ME (2004) State-dependent trapping of flecainide in the cardiac sodium channel. J Physiol 560:37-49 ... Pharmacological characterization of five cloned voltage-gated K+ channels, types Kv1.1, 1.2, 1.3, 1.5, and 3.1, stably ... Benzenesulfonamides act as open-channel blockers on KV3.1 potassium channel. *Carlos Alberto Zanutto Bassetto Junior1, ...