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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
Rimtuzalcap (CAD-1883) V73588 Rimtuzalcap (CAD-1883) 2167246-24-2 Rimtuzalcap (CAD-1883) is a first-in-class, selective PAM (positive allosteric modulator) of small conductance calcium-activated potassium channels (SK channels).
ROMK-IN-32 V73653 ROMK-IN-32 1914944-54-9 ROMK-IN-32 is an inhibitor (blocker/antagonist) of renal outer medullary potassium channels (ROMK) with IC50 of 35 nM.
RU-TRAAK-2 V73602 RU-TRAAK-2 1210538-56-9 RU-TRAAK-2 is a fully reversible TRAAK inhibitor.
RuBi-4AP V73614 RuBi-4AP 851956-02-0 RuBi-4AP is an analogue of 4-aminopyridine (4AP) and a cage Kv channel blocker.
SB705498 V1685 SB705498 501951-42-4 SB-705498 (SB705498; SB 705498) is an orally bioavailable and competitive antagonist of the capsaicin-mediated activation of TRPV1 (transient receptor potential vanilloid 1) receptors with important biological activity.
Sematilide HCl V3851 Sematilide HCl 101526-62-9 Sematilide (formerlyknown as CK-1752) isa novel class III antiarrhythmic agent.
Senicapoc (ICA17043) V14637 Senicapoc (ICA17043) 289656-45-7 Senicapoc, formerly known as ICA-17043, is a highly potent Gardos Channel (Ca2+-activated K+ channel; KCa3.1) inhibitor/blocker with an IC50 of 11 nM, and with the potential for the treatment of a subset of Hereditary Xerocytosis caused by mutations in the Gardos channel.
SKA-31 V14863 SKA-31 40172-65-4 SKA-31 is a potassium channel activator.
Slotoxin V81401 Slotoxin Slotoxin is a bioactive peptide extracted from the venom of the Hoffmann's scorpion Centruroides noxius, which blocks high-conductance calcium-activated potassium channels (potassium channel) with a Kd of 1.5 nM [1].
Sotalol V71346 Sotalol 3930-20-9 Sotalol is an orally bioactive, non-selective beta-adrenoceptor blocker.
Sotalol-d6 (MJ 1999-d6) V71322 Sotalol-d6 (MJ 1999-d6) 1246912-17-3 Sotalol-d6 is the deuterium labelled form of Sotalol.
Spadin TFA V76488 Spadin TFA Spadin TFA, a natural peptide extracted from a propeptide released in the blood, is a potent TREK-1 channel blocker with IC50 of 10 nM.
Spinoxin (Potassium channel toxin alpha-KTx 6.13; SPX; α-KTx6.13) V73611 Spinoxin (Potassium channel toxin alpha-KTx 6.13; SPX; α-KTx6.13) 752984-66-0 Spinoxin, extracted from the venom of the scorpion Heterometrus spinifer, is a 34-residue peptide neurotoxin cross-linked by four disulfide bridges.
SPS-4251 V15184 SPS-4251 870653-45-5 SPS-4251 [PAP-1; SPS4251; 5-(4-Phenoxybutoxy)psoralen] is a novel and potent KCNA3 channel blocker (inhibitor ofKv1.3, voltage-gated K+ channel) with the potential to be usedin treatment of multiple sclerosis.
Ssm spooky toxin (SsTx Toxin) V81436 Ssm spooky toxin (SsTx Toxin) Ssm Spooky Toxin is extracted from Scolopendra mutilans and displays lethal toxicity in the blood and respiratory system by effectively inhibiting KCNQ (voltage-gated potassium channel family 7) channels.
Stromatoxin 1 V73649 Stromatoxin 1 741738-59-0 Stromatoxin 1 is a potassium channel inhibitor, a peptide extracted from tarantulas.
Tamapin V81501 Tamapin Tamapin is a venom peptide that targets small conductance Ca(2+)-activated K(+) (SK) channels.
Tamapin TFA V81502 Tamapin TFA Tamapin TFA is a venom peptide that targets small conductance Ca(2+)-activated K(+) (SK) channels.
Tertiapin LQ V81556 Tertiapin LQ Tertiapin LQ is a specific and reversible inhibitor of the renal outer medullary potassium ROMK1 (Kir1.1) channel.
Tertiapin-RQ V81557 Tertiapin-RQ Tertiapin-RQ is an inward rectifier K+ channel blocker peptide with antidepressant effects.
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