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Cat. No. Product Name Information
PC-38398

Idrevloride

ENaC inhibitor

Idrevloride (P-1037) 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-73070

XPC-6444

NaV1.6 inhibitor

XPC-6444 (XPC6444) is a potent, CNS-penetrant, isoform-selective NaV1.6 inhibitor with IC50 of 41 nM, also potently blocks NaV1.2 (IC50=125 nM).
PC-72898

BI 1265162

ENaC inhibitor

BI 1265162 is a potent ENaC inhibitor, inhibits Na+ transport with IC50 3 nM and 8 nM in M1 and NCI-H441 cells, respectively.
PC-72850

NBI-921352

NaV1.6 inhibitor

NBI-921352 (XEN901, NBI 921352) is a potent, highly selective, orally active inhibitor of NaV1.6 with IC50 of 51 nM (hNaV1.6 channel currents inhibition).
PC-72811

AZ194

CRMP2-Ubc9 inhibitor

AZ194 (CRMP2-Ubc9 inhibitor 194) is a potent and selective inhibitor of NaV1.7 currents in DRG neurons via inhibition of the CRMP2-Ubc9 interaction.
PC-72674

PRAX-562

Persistent INa inhibitor

PRAX-562 (PRAX562) is a novel persistent sodium current (INa) inhibitor, inhibits hNaV1.6 persistent INa induced by ATX-II or SCN8A mutation N1768D with IC50 of 141 and 75 nM, respectively.
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.
PC-72208

SSCI-1

Nav1.7 inhibitor

SSCI-1 is a highly potent, selective NaV1.7 inhibitor with IC50 of 27 and 82 nM on human and rhesus Nav1.7 channels, respectively.
PC-72207

NaV1.7 inhibitor 51

Nav1.7 inhibitor

NaV1.7 inhibitor 51 is a highly potent, selective, orally active NaV1.7 inhibitor with IC50 of 10.7 nM in FLIPR membrane potential assay, no significant activity against NaV1.5 (IC50>10 uM).

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