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Potassium Channel

Potassium Channel

Almost all living things contain potassium channels, which are the most common type of ion channel. They build pores across cell membranes that are selective for potassium. The majority of cell types contain potassium channels, which regulate a wide range of cellular activities. Potassium channels work to quickly and selectively conduct potassium ions down their electrochemical gradient. In many cells, these channels function to either set or reset the resting potential. The delayed counterflow of potassium ions in excitable cells, like neurons, shapes the action potential. Failure of potassium channels can lead to potentially fatal arrhythmias by helping to control the duration of the action potential in cardiac muscle. Maintaining vascular tone may also involve potassium channels.

Potassium Channel related products

Structure Cat No. Product Name CAS No. Product Description
ML365 V4002 ML365 947914-18-3 ML365 is a potent, novel and selective small molecule inhibitor of the TASK1(KCNK3, a two-pore domain potassium channel).
ML402 V4016 ML402 298684-44-3 ML402 (ML-402) is a potent and selective activator of TREK-1/-2and an agonist for OPRM1-OPRD1 (OPRM1: opioid receptor mu 1; OPRD1: delta opioid receptor) heterdimerization.
ML67-33 V73592 ML67-33 1443290-89-8 ML67-33 is a selective activator of temperature- and mechanically-sensitive K2P channels.
Nalanthalide V91075 Nalanthalide 145603-76-5 Nalanthalide is a voltage-gated potassium channel (Potassium Channel) Kv1.3 blocker (IC50=3.9 µM) and potential immunosuppressant.
Nav1.8-IN-7 V89791 Nav1.8-IN-7 2761181-58-0 Nav1.8-IN-7 (Example 116) is a selective Nav1.8 inhibitor.
Nerispirdine V94637 Nerispirdine 119229-65-1 Nerispirdine is an ion channel inhibitor with IC50 values of 3.6, 3.7 and 11.9 μM for K(v)1.1, K(v)1.2 and voltage-dependent Na(+) channels, respectively.
Nicorandil-d4 (Nicorandil d4) V73620 Nicorandil-d4 (Nicorandil d4) 1132681-23-2 Nicorandil-d4 is the deuterium labelled form of Nicorandil.
Noxiustoxin V73657 Noxiustoxin 85205-49-8 Noxiustoxin is a toxin from the venom of the Mexican scorpion Centruroides noxius that blocks voltage-dependent potassium channels (Kv1.3, IC50=360 nM) and calcium-activated potassium channels.
NPBA V85801 NPBA 524033-40-7
NS-11021 V11738 NS-11021 956014-19-0 NS-11021 is a novel, potent and selective activator of large-conductance Ca2+-activated potassium channels (BKCa, KCa1.1).
NS-1643 V2831 NS-1643 448895-37-2 NS1643 is a novel and potent human ether-a-go-go related gene (hERG) KV11 channel activator with EC50 of 10.5 μM.
NS-5806 V21754 NS-5806 426834-69-7 NS-5806 (NS5806) is a novel and potent potassium currentKV4.3 channel activator whichincreases KV4.3/KChIP2 peak current amplitudes with an EC50 of 5.3 μM.
NS1619 V2809 NS1619 153587-01-0 NS-1619 is a selective activator of the large conductance Ca2+-activated K+-channel (BKCa, KCa1.1).
NS19504 V73591 NS19504 327062-46-4 NS19504 is a Ca2+-activated K+ channel (BK channel) activator (EC50=11.0 µM) that has a relaxing effect on spontaneous phasic contractions of bladder smooth muscle.
NS309 V26675 NS309 18711-16-5 NS309 is a nonselective activator of small- and intermediate-conductance Ca2+-activated K+ (SK/KCa2 and IK/KCa3.1) channels (EC50s range from 0.12-1.2 µM for SK channels and 10-90 nM for IK channels).
NS3623 V26676 NS3623 343630-41-1 NS3623 (NS-3623) is a novel and potent (hERG) and KV4.3 channel activator withantiarrhythmic effects.
NS6180 V2816 NS6180 353262-04-1 NS6180 is a novel potent and selective KCa3.1 channel inhibitor with IC50 of 9 nM.
OSK-1 V73654 OSK-1 183815-75-0 OSK-1 is an effective Kv channel blocker, with IC50s of 0.6 nM, 5.4 nM and 0.014 nM for Kv1.1, Kv1.2 and Kv1.3 respectively.
Oxybutynin-d11 chloride (oxybutynin d11 (chloride)) V70540 Oxybutynin-d11 chloride (oxybutynin d11 (chloride)) 1185151-95-4 Oxybutynin-d11 (chloride) is the deuterated form of Oxybutynin chloride.
P-CAB agent 2 V73630 P-CAB agent 2 1978371-23-1 P-CAB agent 2 is a potent and orally bioactive potassium-competitive acid blocker and gastric acid secretion inhibitor.
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