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Cat. No. Product Name Information
PC-70312

RU-TRAAK-2

RU-TRAAK-2 is a completely reversible TRAAK inhibitor, shows no activity for non-K2P channels (Kv1.2, Slo1 and GIRK2).
PC-70311

RU-TRAAK-1

RU-TRAAK-1 is a poorly reversible TRAAK inhibitor, shows no activity for non-K2P channels (Kv1.2, Slo1 and GIRK2).
PC-70310

RU-GIRK-1

GIRK2 inhibitor

RU-GIRK-1 is a potent GIRK2 inhibitor that inhibits GIRK2-mediated flux with an IC50 of 0.35 uM.
PC-60984

ASP2905

KCNH3 inhibitor

ASP 2905 (ASP2905) is a novel potent, selective, orally bioavailable inhibitor of voltage-gated potassium channel KCNH3 with IC50 of 9.0 nM.
PC-60945

TKN2

TREK channel inhibitor

TKN2 is a small molecule allosteric inhibitor of TREK channels with IC50 of 3.8, 1.7 and 10.3 uM for TREK-1, TREK-2 and TRAAK, respectively.
PC-60944

TKN1

TREK channel inhibitor

TKN1 is a small molecule allosteric inhibitor of TREK channels with IC50 of 6.5, 4.4 and 15.7 uM for TREK-1, TREK-2 and TRAAK, respectively.
PC-60943

28NH

TREK channel inhibitor

28NH is a small molecule allosteric inhibitor of TREK channels with IC50 of 5.0, 5.0 and 11.8 uM for TREK-1, TREK-2 and TRAAK, respectively.
PC-60942

TKDC

TREK channel inhibitor

TKDC is a small molecule allosteric inhibitor of TREK channels with IC50 of 4.9, 5.2 and 65.9 uM for TREK-1, TREK-2 and TRAAK, respectively.
PC-60843

SB335573

hERG agonist

SB335573 is a potent, selective hERG potassium channel (Kv11.1) activator.
PC-60842

LUF7244

hERG inhibitor

LUF7244 is a negative allosteric modulator of dofetilide binding to the Kv11.1 (hERG) channel with the strongest effect at 10 uM (IC50=3.9 uM).
PC-60841

VU0405601

hERG activator

VU0405601 is a potent Kv11.1 (hERG) channel allosteric modulator that protects cardiac tissue from hERG-related drug-induced arrhythmias.
PC-60840

PD-118057

hERG activator

PD-118057 is a potent, selective hERG potassium channel (Kv11.1) activator that increases peak tail hERG current of 111.1% at 10 uM in HEK293 cells.

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