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Cat. No. Product Name Information
PC-60572

MRT2000769

Kir7.1 inhibitor

MRT2000769 is a potent Kir7.1 inhibitor with IC50 of 2.0 uM, induces long-lasting uterine contractility similar to those observed with VU590.
PC-60571

VU591

ROMK inhibitor

VU591 is a potent, selective renal outer medullary potassium channel (ROMK, Kir1.1) inhibitor with IC50 of 0.24 uM in T1+ flux assays.
PC-60570

VU590 dihydrochloride

ROMK inhibitor

VU590 is the first small-molecule inhibitor of renal outer medullary potassium channel (ROMK, Kir1.1) and Kir7.1 with IC50 of 294 nM for ROMK.
PC-60569

VU590

ROMK inhibitor

VU590 is the first small-molecule inhibitor of renal outer medullary potassium channel (ROMK, Kir1.1) and Kir7.1 with IC50 of 294 nM for ROMK.
PC-60559

RX 871024

RX 871024 is an imidazoline compound that stimulate insulin release by inhibition of ATP-dependent K+ channels and inducing of Ca2+ mobilization in mouse pancreatic beta-cells.
PC-70220

Paxilline

BKCa inhibitor

Paxilline is a potent blocker of high-conductance Ca2+-activated K+ (BKCa, KCa1.1) channels that binds to the α-subunit of BKCa with Ki of 1.9 nM.
PC-60460

MK-7145

ROMK inhibitor

MK-7145 is a potent, selective, and oral renal outer medullary potassium channel (ROMK, Kir1.1) inhibitor with IC50 of 68 nM.
PC-60338

BL-1249

TREK channel inhibitor

BL-1249 (BL1249) is a potent K2P2.1 (TREK-1) channel activator, enhance the activity of TREK1 currents and produces relaxation of 30 mM KCl-induced contractions in rat bladder strips with EC50 of 1.12 uM.
PC-60337

ML335

TREK-1/2 activator

ML335 (ML 335) is anovel potent, selective K2P2.1 (TREK-1) and K2P10.1 (TREK-2) channels activator with EC50 of 14.3 and 5.2 uM, respectively.
PC-60336

ML402

TREK channel inhibitor

ML402 is a potent, selective K2P2.1 (TREK-1) and K2P10.1 (TREK-2) channels activator with EC50 of 13.7 and 5.9 uM, respectively.
PC-60229

NS15370

Kv.7 activator

NS15370 is a highly potent positive modulator of Kv7 channels with EC50 of 100 nM (Kv7.2-Kv7.5).
PC-60228

ML213

Kv7.2/Kv7.4 activator

ML213 is a potent, selective KCNQ2 (Kv7.2) and KCNQ4 (Kv7.4) activator with EC50 of 230 and 510 nM, respectively.

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