Potassium Channel
Potassium channels are a diverse group of membrane proteins that facilitate the flow of potassium ions (K+) across the cell membrane. These channels play a crucial role in maintaining the resting membrane potential, regulating cell volume, and controlling the excitability of neurons and muscle cells. Potassium channels are involved in various physiological processes, including cardiac rhythm regulation, insulin secretion, and neurotransmitter release. Dysregulation of potassium channels is linked to conditions such as arrhythmias, epilepsy, and hypertension. At CymitQuimica, we offer a wide range of potassium channel modulators to support your research in electrophysiology, cardiovascular health, and neurobiology.
Found 295 products of "Potassium Channel"
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TRAM 39
CAS:TRAM 39 (2-Chloro-α,α-diphenylbenzeneacetonitrile) is a selective blocker of intermediate-conductance Ca2+-activated K+channels.Formula:C20H14ClNPurity:99.97%Color and Shape:SolidMolecular weight:303.78Ref: TM-T23471
1mg34.00€2mg47.00€5mg71.00€10mg102.00€25mg200.00€50mg318.00€100mg502.00€500mg1,063.00€GAL-021 sulfate
CAS:GAL-021 sulfate is a BKCa channel blocker that inhibits the analgesic effects of opioids and is used in the study of respiratory control diseases.Formula:C11H24N6O5SPurity:99.92%Color and Shape:SolidMolecular weight:352.41Nifekalant hydrochloride
CAS:Nifekalant hydrochloride is an IKr potassium channel blocker with an IC50 of 10 µM.Formula:C19H28ClN5O5Purity:99.91%Color and Shape:SolidMolecular weight:441.91Aprikalim
CAS:Aprikalim opens KATP channels, protects the heart, and at high doses, dilates blood vessels.Formula:C12H16N2OS2Purity:99.42% - 99.90%Color and Shape:SolidMolecular weight:268.4Vernakalant Hydrochloride
CAS:Vernakalant Hydrochloride (RSD1235 hydrochloride) is a mixed voltage- and frequency-dependent Na+ and atria-preferred K+ channel blocker.Formula:C20H32ClNO4Purity:99.89%Color and Shape:SolidMolecular weight:385.93Ref: TM-T17227
1mg71.00€2mg92.00€5mg166.00€10mg260.00€25mg495.00€50mg713.00€100mg982.00€1mL*10mM (DMSO)170.00€HN37
CAS:HN37, KCNQ2 activator (EC50=37 nM). Affordable Excellence: Reliable Quality You Can TrustFormula:C20H21FN2O2Purity:99.27%Color and Shape:SolidMolecular weight:340.39Psora 4
CAS:Psora 4 (5-(4-Phenylbutoxy)psoralen) is a Kv1.3 blocker and a caloric restriction mimetic.Formula:C21H18O4Color and Shape:SolidMolecular weight:334.37RY796
CAS:RY796 is a selective voltage-gated potassium (KV2) channel inhibitor that inhibits KV2.1 and KV2.2, used in research on neurological disorders.Formula:C21H27N3O2Purity:98.59%Color and Shape:SolidMolecular weight:353.46ML402
CAS:ML402 (ZINC3671497) is an activator of TREK-1 and TREK-2 with EC50s of 13.7 μM and 5.9 μM.Formula:C14H14ClNO2SPurity:99.71%Color and Shape:SolidMolecular weight:295.78Ref: TM-T16109
5mg48.00€10mg75.00€25mg138.00€50mg215.00€100mg318.00€200mg444.00€1mL*10mM (DMSO)49.00€TWIK-1/TREK-1-IN-3
CAS:TWIK-1/TREK-1-IN-3 is a potassium channel TREK-1 inhibitor TWIK-1/TREK-1-IN-3 has antidepressant activity and can be used to study depression.Formula:C19H27F3N2O2Purity:99.04%Color and Shape:SolidMolecular weight:372.43XE991
CAS:XE991 is a Kv7 (KCNQ) channel blocker.XE 991 dihydrochloride inhibits Kv7.1 (KCNQ1) and M-current and can be used in the study of neurological disorders.Formula:C26H20N2OPurity:98.87%Color and Shape:SolidMolecular weight:376.45DMP-543
CAS:DMP-543 (XR-543) is a potassium channel (KV7 channel) blocker that enhances the release of neurotransmitters.Formula:C26H18F2N2OPurity:99.74%Color and Shape:SolidMolecular weight:412.43RL648_81
CAS:RL648_81 is a selective activator of KCNQ2/3 channels (EC50 = 190 nM). RL648_81 can be used in studies about neuronal hyperexcitability neurologic disorders.Formula:C17H17F4N3O2Purity:99.82%Color and Shape:SolidMolecular weight:371.33SKA-111
CAS:SKA-111 activates KCa3.1 potassium channels, modulates membrane potential in endothelial cells, and dilates rat coronary arteries.Formula:C12H10N2SPurity:99.9%Color and Shape:SolidMolecular weight:214.29Ref: TM-T24799
1mg70.00€5mg153.00€10mg250.00€25mg504.00€50mg727.00€100mg1,017.00€500mg2,043.00€1mL*10mM (DMSO)167.00€ZM 226600
CAS:ZM 226600 is an ATP-sensitive potassium channel opener with an EC50 value of 500 nM. ZM226600 has an inhibitory effect on spontaneous bladder activity.Formula:C16H14F3NO4SPurity:99.87%Color and Shape:SolidMolecular weight:373.35Ref: TM-T23563
2mg34.00€5mg52.00€10mg75.00€25mg138.00€50mg215.00€100mg318.00€200mg444.00€1mL*10mM (DMSO)52.00€PD-118057
CAS:PD-118057, a potent hERG activator, may treat long QT syndrome and heart failure without hERG activity inhibition.Formula:C21H17Cl2NO2Purity:99.95% - 99.97%Color and Shape:SolidMolecular weight:386.27Ref: TM-T16444
1mg84.00€2mg107.00€5mg175.00€10mg263.00€25mg464.00€50mg692.00€100mg1,035.00€200mg1,396.00€1mL*10mM (DMSO)192.00€GW 542573X
CAS:GW 542573X is a potent and selective small molecule Ca2+-activated K+ 2 (SK2) channel activator.GW 542573X induces a leftward shift in the Ca2+ response curveFormula:C19H28N2O5Purity:99.99%Color and Shape:SolidMolecular weight:364.44KT-362 fumarate
CAS:KT-362 fumarate, a novel antagonist of Ca, K, and Na channels, induces vasodilation and relaxes rabbit arterial strips.
Formula:C26H32N2O7SPurity:99.75% - 99.98%Color and Shape:SolidMolecular weight:516.61TASK-1-IN-1
CAS:TASK-1-IN-1: Potent, selective TASK-1 blocker (IC50: 148 nM), weaker on TASK-3 (IC50: 1750 nM), anticancer properties.
Formula:C22H20N2O2Purity:99.57%Color and Shape:SoildMolecular weight:344.41ZTZ240
CAS:ZTZ240 is a KCNQ2 channel activator used in the study of epilepsy.
Formula:C12H8ClFN2OPurity:99.89%Color and Shape:SolidMolecular weight:250.66UK 66914
CAS:UK 66914 is a K(+) channel blocker for the study of cardiac arrhythmias.Formula:C18H24N4O3SPurity:99.75%Color and Shape:SolidMolecular weight:376.47MK-0448
CAS:MK-0448 is a novel and selective blocker of the Kv1.5 (KCNA5) channel, a key channel involved in cardiac repolarization current I Kur.Formula:C24H21FN4O2SPurity:99.25% - 99.79%Color and Shape:SolidMolecular weight:448.51CyPPA
CAS:CyPPA enhances SK channels, reducing firing rate and extending apamin-sensitive afterhyperpolarization.
Formula:C16H23N5Purity:99.88%Color and Shape:SolidMolecular weight:285.39(+)-KCC2 blocker 1
CAS:(+)-KCC2 blocker 1 is a selective blocker of KCC2 (IC50 = 0.4 μM).Formula:C22H25NO5SPurity:99.88%Color and Shape:SolidMolecular weight:415.5Ref: TM-T12504
1mg115.00€2mg172.00€5mg255.00€10mg374.00€25mg562.00€50mg787.00€100mg1,074.00€500mg2,147.00€1mL*10mM (DMSO)284.00€IKs124
CAS:IKs124 is a KCNE2/KCNQ1 potassium channel blocker, for hKCNE1 and hKCNE3, and can be used to study peptic ulcers.Formula:C18H26N2O3SPurity:99.53%Color and Shape:SolidMolecular weight:350.48CLP257
CAS:CLP257 is a selective K+-Cl− cotransporter KCC2 activator (EC50: 616 nM) and it is inactive against NKCC1, GABAA receptors, KCC1, KCC3 or KCC4.
Formula:C14H14FN3O2SPurity:99.5%Color and Shape:SolidMolecular weight:307.34MCHR1 antagonist 2
CAS:MCHR1 antagonist 2 is an antagonist of melanin-concentratin hormone receptor 1(MCH1-R, IC50 = 65 nM) and also inhibits hERG.Formula:C23H21FN2O5Purity:98.29%Color and Shape:SolidMolecular weight:424.42Ref: TM-T11966
2mg43.00€5mg66.00€10mg100.00€25mg210.00€50mg334.00€100mg537.00€200mg710.00€1mL*10mM (DMSO)80.00€P-1075
CAS:P-1075 activates SUR2-KIR6 channels at 45 nM; may open mitoKATP channels and protect the heart.Formula:C12H17N5Purity:99.85%Color and Shape:SolidMolecular weight:231.3Ref: TM-T16420
1mg57.00€5mg119.00€10mg192.00€25mg349.00€50mg530.00€100mg708.00€200mg964.00€1mL*10mM (DMSO)90.00€VU0463271
CAS:VU0463271: KCC2 antagonist, IC50 61 nM, >100x selective over NKCC1, inactive on other GPCRs, channels, transporters.Formula:C19H18N4OS2Purity:97.84% - 99.55%Color and Shape:SolidMolecular weight:382.5Ref: TM-T17243
5mg48.00€10mg75.00€25mg152.00€50mg236.00€100mg350.00€200mg497.00€1mL*10mM (DMSO)To inquireSigma-1 receptor antagonist 3
CAS:Sigma-1 receptor antagonist 3 is a more potent and selective antagonist of Sigma-1 (σ1) receptor (Ki = 1.14 nM) than σ2 receptor(Ki = 1239 nM).Formula:C19H23ClFN3OPurity:99.95%Color and Shape:SolidMolecular weight:363.86Linaprazan
CAS:Linaprazan (AZD0865) inhibits gastric H+,K+-ATPase by K+-competitive binding with an IC50 of 1.0 μM.Formula:C21H26N4O2Purity:99.54%Color and Shape:SolidMolecular weight:366.46DPO-1
CAS:DPO-1 可以高效抑制电压门控钾离子通道Kv1.5，也可以阻断超快速延迟整流钾电流。它能够预防房性心律失常。Formula:C22H29OPPurity:99.78%Color and Shape:SolidMolecular weight:340.44Ref: TM-T22745
5mg46.00€10mg71.00€25mg142.00€50mg205.00€100mg296.00€200mg414.00€1mL*10mM (DMSO)50.00€Glibornuride
CAS:Glibornuride is a blocker of ATP-sensitive K+ channel(pKi: 5.75).Formula:C18H26N2O4SPurity:98.94% - 99.5%Color and Shape:SolidMolecular weight:366.48Ref: TM-T15385
1mg71.00€5mg152.00€10mg236.00€25mg409.00€50mg580.00€100mg803.00€1mL*10mM (DMSO)167.00€11-deoxy-PGF2a
CAS:11-deoxy-PGF2a is a thromboxane A2 receptor agonist that partially alleviates crowding in Lpar3(−/−) female embryos and induces smooth muscle contractionFormula:C20H34O4Color and Shape:SolidMolecular weight:338.48Clobutinol hydrochloride
CAS:Clobutinol hydrochloride, an antitussive agent, influences heart rate and blood pressure, and is utilized in cough-related research [1] [2] [3].Formula:C14H23Cl2NOPurity:98%Color and Shape:SolidMolecular weight:292.25C 101248
CAS:C 101248 (KCNK13-IN-1) is a selective and potent tandem pore halogen inhibitor of K+ channel 1 (THIK-1) inhibitor and a human and mouse KCNK13 inhibitor.Formula:C15H12N6OPurity:99.14% - 99.31%Color and Shape:SolidMolecular weight:292.3Kv3 modulator 1
CAS:Kv3 modulator 1 is a voltage-gated potassium channel Kv3 modulator that can be used to study neurologic-level diseases.Formula:C20H20N4O4Purity:99.41%Color and Shape:SolidMolecular weight:380.4Kv3 modulator 5
CAS:Kv3 modulator 5 (Example 5), a Kv3 channel modulator, enhances the Kv3.2 current and may be employed in research of hearing disorders [1].Formula:C20H20N4O4Color and Shape:SolidMolecular weight:380.4Kv7.2/Kv7.3 modulator-1
CAS:Kv7.2/Kv7.3 modulator-1 (compound 6a) acts as a modulator for Kv7.2/Kv7.3 channels, with a pEC50 value of 7.96 for opening these channels. Kv7.2/Kv7.3 modulator-1 is applicable in research related to epilepsy, depression, brain injury, and pain.Formula:C20H21F4N3O3Color and Shape:SolidMolecular weight:427.393KV1.3-IN-2
CAS:KV1.3-IN-2 (Compound I) selectively inhibits the kv1.3 potassium channel without affecting the hERG channel. It is applicable in research related to immune-associated diseases such as psoriasis, rheumatoid arthritis, and systemic lupus erythematosus.Formula:C16H23ClN2O4Color and Shape:SolidMolecular weight:342.818Opakalim
CAS:Opakalim is an activator of potassium channels (potassium channel) and exhibits anticonvulsant activity.Formula:C18H22F2N4OColor and Shape:SolidMolecular weight:348.39KCC2 Modulator-2
CAS:KCC2 Modulator-2 (example 53) is a regulator of KCC2 with an EC50 of 0.215 μM. It is used in the research of neurological diseases.Formula:C35H45N5O3Color and Shape:SolidMolecular weight:583.76Kv7.2/Kv7.3 agonist 1
CAS:Kv7.2/Kv7.3 agonist 1 (Compound 16) is an orally effective agonist for the KV7.2/7.3 channels (KV7.2/7.3 channel/KCNQ2/3) with an EC50 of 1.03 μM. This compound demonstrates analgesic effects in mouse models of chronic constriction injury (CCI) and Streptozotocin-induced diabetic peripheral neuropathy (DPNP), with ED50 values of 12.02 mg/kg and 9.63 mg/kg, respectively.Formula:C14H14FN3O2Color and Shape:SolidMolecular weight:275.28Kv7.2/Kv7.3 activator-1
CAS:Kv7.2/Kv7.3 Activator-1 (compound 517) serves as a powerful activator of the Kv7.2/Kv7.3 channels, exhibiting an EC50 value of less than 1 µM. It holds potential for use in neurological disease research.Formula:C19H22F2N4OColor and Shape:SolidMolecular weight:360.40cis-KV1.3-IN-1
CAS:cis-KV1.3-IN-1, also known as Compound cis-18, is the cis-isomer of KV1.3-IN-1 and functions as an inhibitor of the KV1.3 channel. In Xenopus laevis oocytes expressing human hKV1.3, cis-KV1.3-IN-1 (10 μM) achieves an inhibition rate of 25.53% against KV1.3.Formula:C23H30N2O4SColor and Shape:SolidMolecular weight:430.56
