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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.
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.
M52713 µ-Conotoxin GIIIB μ-Conotoxin GIIIB is a 22-residue polypeptide that can be isolated from the venom of piscivorous cone snail Conus geographus.
M52712 µ-Conotoxin BuIIIC μ-Conotoxin BuIIIC (Mu-Conotoxin BuIIIC) is a potent Nav1.4 inhibitor.
M52711 µ-Conotoxin BuIIIB μ-Conotoxin BuIIIB (Mu-Conotoxin BuIIIB) is a mammalian neuronal voltage-gated sodium channel (VGSC) blocker.
M52710 μ-Conotoxin Sx IIIA μ-Conotoxin Sx IIIA is a biological active peptide.
M52709 Hainantoxin-III Jingzhaotoxin-V is a peptide that inhibits potassium currents in Xenopus laevis oocytes with an IC50 value of 604.2 nM.
M52708 Hainantoxin-IV Hainantoxin-IV is a specific antagonist of Sodium Channel, targeting to tetrodotoxin-sensitive (TTX-S) voltage-gated sodium channels.
M52707 Ceratotoxin-2 Ceratotoxin-2 (CcoTx2) is a voltage-gated sodium channel blocker with IC50s of 8 nM and 88 nM against Nav1.2/β1 and Nav1.3/β1, respectively.
M52706 Mambalgin 1 Mambalgin-1 is a toxin isolated from black mamba venom.
M52705 GpTx-1 GpTx-1 is a potent and selective NaV1.7 antagonist with an IC50 of 10 nM.
M49943 PF-06305591 dihydrate PF-06305591 dihydrate is a potent, highly selective blocker of the voltage-gated sodium channel NaV1.8 with an IC50 value of 15 nM for pain-related studies.
M49942 PF-06305591 PF-06305591 is a potent and highly selective blocker of the voltage-gated sodium channel NaV1.8 with an IC50 value of 15 nM for pain-related studies.
M49941 VX-128 VX-128 is a Nav1.8 blocker that can be used in studies related to acute pain.
M49823 PRAX-628 PRAX-628 is a potential best-in-class, selective small molecule inhibitor of sodium channels that targets sodium channels in the brain in a hyperexcitable state. It can be used in studies related to focal epilepsy.
M49486 BI 1265162 BI 1265162 is a selective epithelial sodium channel (ENaC) inhibitor for studies related to cystic fibrosis (CF).




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