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Cat. No. Product Name Information
PC-62647

Diminazene aceturate

ASIC1a inhibitor

Diminazene aceturate is an anti-infective agent, also is a slow pore blocker of acid-sensing ion channel 1a (ASIC1a) with IC50 of 0.3 uM.
PC-62325

GNE-0439

Nav1.7 inhibitor

GNE-0439 is a novel potent, selective inhibitor of Nav1.7 channel with IC50 of 0.34 uM, shows high selectivity over Nav1.5 (IC50=38.3 uM).
PC-62324

GX-936

NaV1.7 inhibitor

GX-936 (PF 05196233) is a potent Nav1.7 inhibitor that binds to the activated state of voltage-sensor domain IV (VSD4), exhibits robust inhibition of the 1KαPMTX-evoked N1742K response with IC50 of 40 nM.
PC-62323

GX-674

Nav1.7 inhibitor

GX-674 is a potent, selective Nav1.7 inhibitor with IC50 of 0.1 nM.
PC-61870

PF-04531083

Nav1.8 inhibitor

PF-04531083 (PF 4531083) is a potent and selective, orally available sodium channel Nav1.8 blocker for treatment of pain.
PC-61869

XEN-402

XEN-402 (Funapide,TV-45070) is a potent and selective, orally available sodium channel Nav1.7 and Nav1.8 blocker for treatment of pain.
PC-61857

PF-05241328

NaV1.7 inhibitor

PF-05241328 (PF 5241328) is a potent and selective, orally active inhibitor of voltage-dependent sodium channel Nav1.7 with IC50 of 31 nM.
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.

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