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Cat. No. Product Name Information
PC-47508

Benzocaine

Sodium channel inhibitor

Benzocaine is a local anesthetic, inhibits voltage-dependent sodium channels (VDSCs) on the neuron membrane, stopping the propagation of the action potential.
PC-45927

Proparacaine hydrochloride

Sodium channel inhibitor

Proparacaine hydrochloride (Proxymetacaine hydrochloride) is an irreversible local anesthetic, inhibits pain sensations that is believed to act as an antagonist on voltage-gated sodium channels.
PC-45625

Nav1.7-IN-2

NaV1.7 inhibitor

Nav1.7-IN-2 is a potent, selective inhibitor of voltage-gated sodium channel Nav1.7 (IC50=80 nM), extracts from patent WO/2011103196 A1, compound example J.
PC-45224

Ranolazine dihydrochloride

Sodium channel inhibitor

Ranolazine dihydrochloride is an anti-ischemic agent that has been shown to inhibit late I(Na) and I(Kr) and to have antiarrhythmic effects in various preclinical in vitro models.
PC-42318

ETH2120

Sodium ionophore

ETH2120 is a sodium ionophore, relieves hydrogen-dependent caffeate reduction and completely abolishes ATP synthesis in cells.
PC-42201

Nicainoprol

Sodium channels inhibitor

A sodium channels blocker, adrenergic receptor antagonist and class 1 antiarrhythmic agent..
PC-45079

ICA-121431

Nav1.3/Nav1.1 inhibitor

A potent, selective small molecule human Nav1.3/Nav1.1 channel inhibitor with IC50 of 19 nM.
PC-45762

XEN-907

NaV1.7 inhibitor

XEN-907 (XEN907) is a potent, selective NaV1.7 blocker with IC50 of 3 nM.
PC-42804

A-803467

Nav1.8 inhibitor

A-803467 (A803467) potent and selective Nav1.8 sodium channel blocker with IC50 of 8 nM.
PC-45068

Eleclazine hydrochloride

Sodium current inhibitor

A novel, potent, and selective inhibitor of Late sodium current (late INa) for treatment of long QT-3 syndrome (LQT-3), hypertrophic cardiomyopathy (HCM), and ventricular tachycardia–ventricular fibrillation (VT–VF).
PC-45252

Flecainide acetate

Nav1.5 inhibitor, RyR2 inhibitor

A class Ic antiarrhythmic agent used to prevent and treat tachyarrhythmias, works by blocking the Nav1.5 sodium channel in the heart, slowing the upstroke of the cardiac action potential.
PC-23462

ETD001

ENaC inhibitor

ETD001 is a potent, selective epithelial sodium channel (ENaC) inhibitor with IC50 of 57 nM.

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