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Cat. No. Product Name Information
PC-20055

BI-9267

NHE1/SLC9A1 inhibitor

BI-9267 is a potent, selective antagonist of the sodium-hydrogen antiporter 1 (NHE1, SLC9A1).
PC-49611

A-887826

Nav 1.8 blocker

A-887826 (A 887826) is a potent and voltage-dependent Na(v)1.8 sodium channel blocker with IC50 of 11 nM (hNav1.8), potently blocks tetrodotoxin-resistant sodium (TTX-R Na(+)) currents (IC50=8 nM) from small diameter rat DRG neurons.
PC-47037

QX-314 bromide

QX 314 bromide is a membrane impermeable quaternary derivative of lidocaine, a blocker of voltage-activated Na+ channels, also inhibits calcium currents in hippocampal CA1 pyramidal neurons.
PC-47030

BW-031 iodide

Nav1.7 inhibitor

BW-031 iodide is a potent cationic sodium channel inhibitor, inhibited Nav 1.7 (IC50=9.5 uM) and Nav 1.1 channels with approximately sixfold greater potency than QX-314.
PC-47029

BW-031 chloride

Nav1.7 inhibitor

BW-031 chloride is a potent cationic sodium channel inhibitor, inhibited Nav 1.7 (IC50=9.5 uM) and Nav 1.1 channels with approximately sixfold greater potency than QX-314.
PC-38569

DPI 201-106

Na+ channel opener

DPI 201-106 (SDZ 201106) is a positive inotropic agent that prolongs the open state of cardiac voltage-gated Na+ channels.
PC-38398

Idrevloride

ENaC inhibitor

Idrevloride is a potent, selective epithelial sodium channel (ENaC) blocker with potential for the treatment of skin disorders.
PC-73408

Bliretrigine

Sodium Channel inhibitor

Bliretrigine is a sodium channel blocker with the effect of relieving pain.
PC-73335

ASIC1a inhibitor 5b

ASIC1a inhibitor

ASIC1a inhibitor 5b is a highly selective and potent ASIC1a inhibitor, inhibits proton-evoked ASIC1a currents with an apparent IC50 of 27 nM at pH 6.7.
PC-73334

Psalmotoxin 1

ASIC1a inhibitor

Psalmotoxin 1 (PCTX1) is a potent and selective acid-sensing ion channel 1a (ASIC1a) blocker with IC50 of 0.9 nM.
PC-72811

NaV1.7 inhibitor Compound 194

NaV1.7 inhibitor

NaV1.7 inhibitor Compound 194 is a potent and selective inhibitor of NaV1.7 currents in DRG neurons via inhibition of the CRMP2-Ubc9 interaction.
PC-72209

SSCI-2

Nav1.7 inhibitor

SSCI-2 is a highly potent, selective NaV1.7 inhibitor with IC50 of 9 and 17 nM on human and rhesus Nav1.7 channels, respectively.

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