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Sodium Channel Sodium Channel

Cat.No.  Name Information
M3386 Amiloride hydrochloride Amiloride hydrochloride, a pyrazine compound inhibiting sodium reabsorption through sodium channels in renal epithelial cells.
M3366 Amiloride hydrochloride dihydrate Amiloride Hydrochloride Dihydrate (MK-870 Hydrochloride Dihydrate) is an inhibitor of epithelial sodium channel (ENaC) and urokinase-type plasminogen activator receptor (uTPA). Amiloride hydrochloride dihydrate is polycystin-2 (PC2; TRPP2) channel blocker.
M58140 HwTx-IV Huwentoxin-IV (HwTx-IV) is a 35-residue neurotoxin peptide with potential application as a novel analgesic. Huwentoxin-IV, a component of tarantula venom, potently blocks sodium channels and is an attractive scaffold for engineering a Nav1.7-selective molecule.
M42248 ProTx II TFA ProTx II TFA is a selective blocker of Nav1.7 sodium channels with an IC50 of 0.3 nM, and is at least 100-fold selective for Nav1.7 over other sodium channel subtypes.
M5069 S0859 S0859 is an N-cyanosulphonamide compound, reversibly inhibit NBC-mediated pH(i) recovery (K (i)=1.7 microM, full inhibition at approximately 30 microM).
M5897 Prilocaine Prilocaine is a local anesthetic of the amino amide type. It acts on sodium channels on the neuronal cell membrane, limiting the spread of seizure activity and reducing seizure propagation.
M56574 A-317567  A-317567 is a potent acid-sensing ion channel 3 (ASIC-3) inhibitor with an IC50 of 1.025 μM.
M56573 XPC-6444  XPC-6444 is a highly potent, isoform-selective, and CNS-penetrant NaV1.6 inhibitor (IC50=41 nM for hNaV1.6).
M56572 TC-N 1752  TC-N 1752 is a potent and orally active inhibitor of Nav1.7, with IC50s of 0.17 μM, 0.3 μM, 0.4 μM, 1.1 μM and 2.2 μM at hNav1.7, hNav1.3, hNav1.4, hNaV1.5 and rNav1.8, respectively.
M56571 Nav1.8-IN-4  Nav1.8-IN-4 is a Nav1.8 channel inhibitor (IC50=0.014 μM).
M56570 MTSEA-Fluorescein  MTSEA-Fluorescein is a fluorescent probe that can be used for ion channel research.
M56569 Suzetrigine phenol  Suzetrigine phenol is the phenolate form of the sodium channel modulator Suzetrigine.
M56568 KC 12291 hydrochloride  KC 12291 hydrochloride is an orally active blocker of voltage-gated sodium channel (VGSC).
M56567 NaV1.2/1.6 channel blocker-1  NaV1.2/1.6 channel blocker-1 is a potent NaV1.2/1.6 channel blocker, with IC50s of 9.8 and 24.4 μM for rNaV1.6 and hNaV1.2, respectively.
M54821 ASN008 ASN008 is a permanently positively charged sodium channel blocker.
M53703 Psalmotoxin 1 Psalmotoxin 1 (PcTx1) is a protein toxin that can bind at subunit-subunit interfaces of acid-sensing ion channel 1a (ASIC1a).
M52723 Jingzhaotoxin-III Jingzhaotoxin-III is a potent and selective blocker of Nav1.5 channels, with an IC50 of 348 nM, and shows no effect on other sodium channel isoforms.
M52722 Huwentoxin-IV Huwentoxin-IV is a potent and selective sodium channel blocker, inhibits neuronal Nav1.7, Nav1.2, Nav1.3 and Nav1.4 with IC50s of 26, 150, 338 and 400 nM, respectively.
M52721 Phrixotoxin 3 Phrixotoxin 3 is a potent blocker of voltage-gated sodium channels, with IC50s of 0.6, 42, 72, 288, 610 nM for NaV1.2, NaV1.3, NaV1.4, NaV1.1 and NaV1.5, respectively.
M52720 APETx2 APETx2, a sea anemone peptide from Anthopleura elegantissima, is a selective and reversible ASIC3 inhibitor, with an IC50 of 63 nM.
M52719 β-Pompilidotoxin β-Pompilidotoxin (β-PMTX), a wasp venom, can slow sodium channel inactivation and increases steady-state sodium current in cells.
M52718 µ-Conotoxin-CnIIIC μ-Conotoxin-CnIIIC is a 22-residue conopeptide that can be isolated from Conus consors.
M52717 µ-Conotoxin KIIIA μ-Conotoxin KIIIA is an analgesic μ-conotoxin that can be isolated from Conus kinoshitai.
M52716 µ-Conotoxin SIIIA μ-Conotoxin SIIIA is a tetrodotoxin (TTX)-resistant sodium channel blocker.
M52715 ω-Conotoxin CVIB ω-Conotoxin CVIB is a non-selective N- and P/Q-type voltage-gated calcium channels (VGCCs) antagonist.
M52714 μ-Conotoxin PIIIA μ-Conotoxin PIIIA is a sodium channel (NaV 1.4) blocker.




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