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Cat. No. Product Name Information
PC-61854

AZD-3161

NaV1.7 inhibitor

AZD-3161 (AZD3161) is a potent and selective sodium channel Nav1.7 blocker with pIC50 of 7.1, >100-fold selective over NaV1.5.
PC-61853

PF-04856264

NaV1.7 inhibitor

PF-04856264 is a potent, selective Nav1.7 blocker with IC50 of 28 nM, dispalys >1,000-fold selectivity over Nav1.5.
PC-61336

Lacosamide

Sodium channel inhibitor

Lacosamide (SPM 927) is an anticonvulsant compound that enhances the slow inactivation of voltage-gated sodium channels without affecting the fast inactivation of voltage-gated sodium channels.
PC-60629

AMG 8379

NaV1.7 inhibitor

AMG 8379 (AMG-8379, AMG8379) is a potent and selective voltage-gated sodium channel Nav1.7 antaognist with IC50 of 8.5 nM.
PC-70213

Flecainide

Nav1.5 inhibitor, RyR2 inhibitor

Flecainide is 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-60194

AnCoA4

Orai1 channel inhibitor

AnCoA4 (AnCoA-4, Jamaicin) is a potent Orai1 channel inhibitor that inhibits store-operated calcium (SOC) with EC50 of 0.88 uM.
PC-60005

A-317567

A-317567 (A317567) is a novel potent acid sensing ion channel (ASIC) blocker with IC50 of 2-30 uM.
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.

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