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Potassium Channel

Potassium Channel

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Cat. No.	Product Name	CAS No.	Information
CSN25578	VU590 2HCl	1783987-83-6	VU590 dihydrochloride has been reported to inhibit the renal, outer medullary potassium channel (KIR1.1) with IC50 of 294 nM, and also able to inhibit the inward rectifying potassium channel KIR7.1.
CSN25562	VU590	313505-85-0	VU590 dihydrochloride has been reported to inhibit the renal, outer medullary potassium channel (KIR1.1) with IC50 of 294 nM, and also able to inhibit the inward rectifying potassium channel KIR7.1.
CSN23185	VU 0463271	1391737-01-1	VU0463271 is a potent KCC2 antagonist, with an IC50 of 61 nM.
CSN12970	Vernakalant HCl	748810-28-8	Vernakalant HCl prolongs repolarization by blocking atrial potassium channels its a class III antiarrhythmics
CSN12056	Terfenadine	50679-08-8	Terfenadine is a potent open-channel blocker of hERG with a mean IC50 of 204 nM.
CSN23324	Tannic Acid	5424-20-4	Tannic acid is a novel hERG channel blocker with IC50 of 3.4 μM.
CSN16112	TAK-438	1260141-27-2	TAK-438, a potassium proton pump inhibitor, can reversibly inhibit HK ATPase with IC50 of 17 nM and does not affect NaK ATPase. It also controls gastric acid secretion.
CSN16469	Sophocarpine	6483-15-4	Sophocarpine is a naturally-occuring HERG K channel blocker with IC50 ranging in 100-300 M found from plant Sophora flavescens
CSN11584	Repaglinide	135062-02-1	Repaglinide is a carbamoylmethyl benzoic acid (CMBA) derivative, which recently has become available for the treatment of type II diabetes.
CSN16137	Quinine	130-95-0	Quinine is a medication used to treat malaria and babesiosis, isolated from the bark of a cinchona tree.
CSN21820	Quinidine HCl H2O	6151-40-2	Quinidine HCl H2O is a class IA antiarrhythmic and a blocker of potassium channel.
CSN23838	Pinacidil H2O	85371-64-8	Pinacidil monohydrate, an antihypertensive drug, is a potassium channel activator.
CSN21725	Peptide 401	32908-73-9	Peptide 401 is a blocker of voltage-sensitive K⁺ channels with convulsant activity.
CSN10033	PAP-1	870653-45-5	PAP-1 is a selective inhibitor of Kv1.3, voltage-gated K channel, it potently inhibits human T effector memory cell proliferation with EC50 of 2 nM and delayed hypersensitivity.
CSN25559	NS 5806	426834-69-7	NS5806, a KV4.3 channel activator, increases peak current amplitude of the potassium channel Kv4.3 with EC50 of 5.3 uM. NS5806 also slows Kv4.3 and Kv4.2 current dacay in channel complexes containing KChIP2.
CSN25560	NS19504	327062-46-4	NS19504 is a selective activator of large-conductance Ca2+-activated potassium channels (BKCa, KCa1.1) with EC50 of 11 μM.
CSN18234	NS-6180	353262-04-1	NS-6180 is a channel blocker of KCa3.1 (IC50 9 nM for rat and 14 nM for human). It can prevent T-cell activation and inflammation.
CSN12478	Nateglinide	105816-04-4	Nateglinide is an insulin secretagog agent used for the treatment of non-insulin-dependent diabetes mellitus (NIDDM).
CSN25288	ML 297	1443246-62-5	ML 297 is a potent and selective GIRK1/2 activator, with an EC50 of 0.16 μM.
CSN18790	Mitiglinide Calcium Hydrate	207844-01-7	Mitiglinide calcium is a drug for the treatment of type 2 diabetes and it is a highly selective KATP channel antagonist.
CSN12556	Mitiglinide Calcium	145525-41-3	Mitiglinide calcium is a blood glucose-lowering drugs, stimulating insulin secretion by closing the ATP-sensitive K channels in pancreatic beta-cells.
CSN10129	Minoxidil Sulfate	83701-22-8	Minoxidil sulfate is a K channel agonist and a strong vascular smooth muscle relaxant It has been shown to relax norepinephrine contraction and is reported to be a vasodilator Minoxidil sulfate has been used to better understand the blood-brain tumor barrier in syngeneic and allogeneic rat studies and has demonstrated to increase tumor permeability
CSN21733	Micinicate	39537-99-0	Micinicate, a local anesthetic, can reversibly block transient Na⁺ inward current as well as the steady-state K⁺ outward current.
CSN21708	Levcromakalim	94535-50-9	Levcromakalim is an activator of ATP-sensitive K⁺ channel (KATP).
CSN24792	IK1 inhibitor PA-6	500715-03-7	IK1 inhibitor PA-6 (PA-6), a pentamidine analogue, is a selective and potent IK1 (KIR2.x ion-channel-carried inward rectifier current) inhibitor, with IC50 values of 12-15 nM for human and mouse KIR2.x currents. IK1 inhibitor PA-6 (PA-6) elevates KIR2.1 protein expression and induces intracellular KIR2.1 accumulation. IK1 inhibitor PA-6 (PA-6) has the potential to treat atrial fibrillation and arrhythmia[1][2][3].
CSN25242	ICA 110381	325457-99-6	ICA 110381 is a KV7.2/7.3 activator with EC50 of 0.38 μM.
CSN24161	GSK369796 2HCl	1010411-21-8	GSK369796 2HCl is an affordable and effective antimalarial and inhibits hERG potassium ion channel repolarization with an IC50 of 7.5 μM.
CSN11101	Glipizide	29094-61-9	Glipizide is used to treat high blood sugar levels caused by a type of diabetes mellitus called type 2 diabetes.
CSN10055	Glibenclamide	10238-21-8	Glibenclamide is a sulfonylurea compound that modulates insulin production
CSN22064	GAL-021	1380341-99-0	GAL-021 a new intravenous Potassium Channel KCa1.1 blocker.
CSN12647	Diazoxide	364-98-7	Diazoxide is an ATP-sensitive potassium channel activator which causes local relaxation in smooth muscle by increasing membrane permeability to potassium ions. and can be used to treat hyperinsulinism.
CSN10772	Dequalinium Chloride	522-51-0	Dequalinium Chloride is a PKC inhibitor with IC50 of 7-18 M, and also a selective blocker of apamin-sensitive K channels with IC50 of 1.1 M.
CSN15660	Daurisoline	70553-76-3	Daurisoline, a natural product isolated and purified from the roots of Menispermum dauricu with antiarrhythmic effects, exerts a blocking effect on hERG at concentrations below 30 uM, but does not affect the expression and function of the hERG channel.
CSN24262	CLP-290	1181083-81-7	CLP-290 is a highly selective KCC2 modulator and prodrug of CLP-257.
CSN23809	Cloperastine Fendizoate	85187-37-7	Cloperastine fendizoate inhibits the hERG K+ currents in a concentration-dependent manner with an IC50 value of 27 nM.
CSN13101	Chlorzoxazone	95-25-0	Chlorzoxazone, a potassium channel activator, is a centrally acting muscle relaxant used to treat muscle spasm and the resulting pain or discomfort.
CSN23891	AUT1	1311136-84-1	AUT1 is a Kv3 potassium channel modulator with pEC50 values of 5.33 and 5.31 for human recombinant Kv3.1b and Kv3.2a, respectively.
CSN21493	Apamin	24345-16-2	Apamin, an 18 amino acid peptide toxin found in bee venom, is a potent blocker of small conductance Ca²⁺-activated K+ (SK, KCa2) channels.
CSN19508	Amifampridine	54-96-6	Amifampridine is a quaternary ammonium compound that blocks presynaptic potassium channels, subsequently prolongs the action potential and increases presynaptic calcium concentrations, it was approved by the US FDA for the treatment of adults with LEMS.
CSN24263	AM 92016 hydrochloride	133229-11-5	AM 92016 is a K_V channel blocker.
CSN21132	Almitrine Mesylate	29608-49-9	Almitrine mesylate is an agonist of peripheral chemoreceptor and inhibits selectively the Ca2-dependent K channel. It can improve chronic obstructive pulmonary disease and nocturnal oxygen desaturation.
CSN10068	Ajmaline	4360-12-7	Ajmaline, a natural alkaloid isolated and purified from the roots of Rauvolfia verticillata, is a class Ia antiarrhythmic agent.
CSN25278	A2793	88349-90-0	A2793 is an inhibitor of TRESK (IC50 value of 6.8 μM for mTRESK).
CSN25279	A2764 2HCl	861038-72-4	A2764 dihydrochloride is a selective inhibitor of TRESK (KCNK18) with an IC50 value of 11.8 μM. A2764 can inhibit TRESK in native cells, leading to cell depolarization and increased excitability.
CSN25420	ML335	825658-06-8
CSN25450	JNJ 303	878489-28-2
CSN25449	Tetraethylammonium bromide	71-91-0
CSN25452	1-EBIO	10045-45-1
CSN25451	Tetraethylammonium chloride	56-34-8

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Potassium Channel

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