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. |