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首页-小分子抑制剂&激动剂-Membrane Transporter/Ion Channel-Sodium Channel

Request The Product List ofSodium Channel Sodium Channel

Cat. No. Product Name Information
PC-22424

ANP-230

Nav1.7/1.8/1.9 inhibitor

ANP-230 (DSP-2230) is a selective sodium channel blocker of human Nav1.7, Nav1.8, and Nav1.9 with IC50 of 7.1, 11.4, and 6.7 μM (sodium currents), shows only low inhibitory activity to human cardiac Nav1.5 channel and rat central Nav channels.
PC-21779

XPC-5462

NaV1.2/1.6 inhibitor

XPC-5462 is a potent, selective dual inhibitor of NaV1.6 and NaV1.2 with IC50 of 10.9 nM and 10.3 nM, respectively.
PC-21778

XPC-7224

NaV1.6 inhibitor

XPC-7224 is a potent, selective NaV1.6 inhibitor with IC50 of 78 nM and 130 nM for human and mouse NaV1.6, respectively, interacts with the inactivated state of the channel.
PC-21678

LTGO-33

NaV1.8 inhibitor

LTGO-33 is a potent, selective inhibitor of voltage-gated sodium channel NaV1.8 with IC50 of 44 nM (hNaV1.8), 600-fold selectivity against NaV1.1-NaV1.7 and NaV1.9.
PC-20850

DS43260857

NaV1.7 inhibitor

DS43260857 is a potent, selective NaV1.7 inhibitor with IC50 of 15 nM (hNaV1.7), shows 440-fold and 930-fold selectivity over hNaV1.1 and hNaV1.5, respectively.
PC-49611

A-887826

Nav 1.8 inhibitor

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-49224

AM-0466

NaV1.7 inhibitor

AM-0464 (AM0464) is a highly potent, selective NaV1.7 inhibitor with IC50 of 21 nM, exhibits high levels of selectivity over other sodium channel isoforms (NaV1.5, IC50>30 uM).
PC-47037

QX-314 bromide

Sodium channel inhibitor

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-47036

QX-314 chloride

Sodium channel blocker

QX 314 chloride 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, inhibits Nav 1.7 (IC50=9.5 uM) and Nav 1.1 channels with approximately sixfold greater potency than QX-314.
PC-38662

ABBV-318

Nav1.7/ Nav1.8 blocker

ABBV-318 is a small molecule voltage-gated sodium channel Nav1.7/ Nav1.8 blocker with IC50 of 3.8 and 2.8 uM for hNav1.7 and hNav1.8 in FRET assays, respectively.

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