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Cat. No. Product Name Information
PC-26171

Apamin TFA

SK channel inhibitor

Apamin (Apamine) TFA is a peptide neurotoxin found in apitoxin and selective small conductance Ca(2+)-activated K(+) (SK(Ca)) channel blocker, exhibits anti-inflammatory and anti-fibrotic activity.
PC-26170

Apamin

SK channel inhibitor

Apamin (Apamine) is a peptide neurotoxin found in apitoxin and selective small conductance Ca(2+)-activated K(+) (SK(Ca)) channel blocker, exhibits anti-inflammatory and anti-fibrotic activity.
PC-26105

ICA73

KCNQ2 activator

ICA‐069673 (ICA73) is a selective activator of KCNQ2 potassium channel (Kv7.2), acts within the voltage-sensor domain (VSD), shows selective effects on KCNQ2 over KCNQ3.
PC-26104

ztz240

KCNQ2 activator

ztz240 is a potent, selective activator of KCNQ2 potassium channel (Kv7.2) with EC50 of 5.8 uM on outward current of KCNQ2 channels.
PC-26103

E0714

Kv7.2 agonist

E0714 (E-0714) is a potent, specific agonist of Kv7.2 potassium channel (KCNQ2) with EC50 of 1.9 uM and 0.021 uM for Kv7.2 and Kv7.2/7.3 currents, with no significant activation of Kv7.1/7.3/7.4/7.5.
PC-25953

SK2 channel activator Compound 4

SK2 channel activator

SK2 channel activator Compound 4 is a potent, selective activator of small conductance calcium-activated potassium channel 2 (SK2), dose-dependently increases SK2 current in the presence of 2 µM intracellular Ca2+.
PC-25952

SK2 channel inhibitor Compound 1

SK2 channel inhibitor

SK2 channel inhibitor Compound 1 is a potent, selective inhibitor of small conductance calcium-activated potassium channel 2 (SK2) with IC50 of 69 nM, with 10-fold reduced potency for SK4 (IC50=660 nM), has high selectivity over other ion channels tested including hERG, Nav1.5, KCNQ1, and Cav1.2.
PC-25626

ONO-7927846

TERK inhibitor

ONO-7927846 (VU6024391) is a selective and CNS penetrant TWIK-related K+ channels (TREK) inhibitor with IC50 of 110 nM and 290 nM for human TREK-1 and TREK-2 in thallium flux assays respectively.
PC-25625

ONO-9517601

TERK inhibitor

ONO-9517601 (VU6022856) is a selective and CNS penetrant TWIK-related K+ channels (TREK) inhibitor with IC50 of 67 nM and 230 nM for human TREK-1 and TREK-2 in thallium flux assays respectively.
PC-25574

VU6080824

Kir2.1 inhibitor

VU6080824 is a potent, selective inhibitor of the inward-rectifier potassium channel Kir2.1 with IC50 of 5.9 uM in Kir2.1 thallium flux assays, selective relative to Kir1.1 and Kir4.1 up to 10 uM.
PC-25544

VU6032735

SLO3 inhibitor

VU6032735 is a highly potent, subtype-selective sperm-specific potassium channel 3 (SLO3) inhibitor with IC50 of 165 nM (hSLO3), 172-fold selective over hERG.
PC-25468

DCY1020

TMEM175 agonist

DCY1020 is a potent, specific small molecule agonist of transmembrane protein 175 (TMEM175) with EC50 of 3.7 uM, binds to TMEM175 with SPR KD of 8.3 uM.

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