Home Tools
Log in
Cart

Potassium Channel

Potassium Channels. K+ channels are membrane proteins that allow rapid and selective flow of K+ ions across the cell membrane, and thus generate electrical signals in cells. Voltage-gated K+ channels (Kv channels), present in all animal cells, open and close upon changes in the transmembrane potential.
Signaling Pathways | Target | TargetMol
Cat. No. Product name CAS No. Purity Chemical Structure
T4316 ML365 947914-18-3 99.91%
ML365
ML365 is a novel selective small molecule inhibitor of TASK1(KCNK3).
T72066 CHET3 2489231-47-0 99.91%
CHET3
CHET3 is a TASK-3 inhibitor that can be used to study pain.
T1073 Dronedarone hydrochloride 141625-93-6 99.91%
Dronedarone hydrochloride
Dronedarone hydrochloride (SR33589) is an amiodarone analog which has an effective and promising treatment for Atrial fibrillation.
T22826 GW 542573X 660846-41-3 99.91%
GW 542573X
GW 542573X is a potent and selective small molecule Ca2+-activated K+ 2 (SK2) channel activator.GW 542573X induces a leftward shift in the Ca2+ response curve of...
T3876 Loureirin B 119425-90-0 99.91%
Loureirin B
Loureirin B can downregulate the expression of fibrosis-related molecules by regulating MMPs and TIMPs levels, inhibit scar fibroblast proliferation and suppress...
TQ0150 Levcromakalim 94535-50-9 99.91%
Levcromakalim
Levcromakalim (BRL 38227) is an activator of the ATP-sensitive K+ channel.
T3054 Daurisoline 70553-76-3 99.90%
Daurisoline
Daurisoline ((R,R)-Daurisoline) is a hERG inhibitor. Daurisoline is also an autophagy blocker.
T13320L VU591 1222810-74-3 99.9%
VU591
1222810-74-3
T10977 DCEBIO 60563-36-2 99.89%
DCEBIO
DCEBIO stimulates the secretion of Cl- through the activation of the hIK1 K + channel and the activation of the apical Cl- conductance. DCEBIO is a derivative of...
T1050 Prazosin hydrochloride 19237-84-4 99.87%
Prazosin hydrochloride
Prazosin hydrochloride (Vasoflex) reduces peripheral resistance and relaxes vascular smooth muscles as a selective adrenergic alpha-1 antagonist by a mechanism n...
T27753 KT-362 fumarate 105394-80-7 99.87%
KT-362 fumarate
KT-362 fumarate is a novel compound that acts as an antagonist of calcium channels, potassium channels and sodium channels.KT-362 fumarate causes vasodilation by...
TN1092 O-Nornuciferine 3153-55-7 99.86%
O-Nornuciferine
O-Nornuciferine reveals distinct in vitro hERG blockages measured in HEK293 cells with the IC50 value of 2.89 uM.
T8182 Guanfu base A 1394-48-5 99.85%
Guanfu base A
Guanfu base A is a potent noncompetitive CYP2D6 inhibitor (Ki: 1.20 μM in HLMs; Ki: 0.37 μM for rCYP2D6). It also inhibits HERG channel current.
T2170 SKF-96365 hydrochloride 130495-35-1 99.85%
SKF-96365 hydrochloride
SKF-96365 hydrochloride (SKF96365) , a SOCE inhibitor, exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal Y cells...
T12256 NS8593 hydrochloride 875755-24-1 99.83%
NS8593 hydrochloride
NS8593 hydrochloride (NS8593 HCl) is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels) .
T2280 Endoxifen (Z-isomer) 112093-28-4 99.81%
Endoxifen (Z-isomer)
Endoxifen Z-isomer (EDX) is a key active metabolite of tamoxifen (TAM) with higher affinity and specificity to estrogen receptors that also inhibits aromatase ac...
T6592 ML133 hydrochloride 1222781-70-5 99.81%
ML133 hydrochloride
ML133 hydrochloride (ML133 HCl) is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 a...
T1676 Rosuvastatin 287714-41-4 99.8%
Rosuvastatin
Rosuvastatin (ZD 4522) is an antilipemic agent that competitively inhibits hydroxymethyl-glutaryl-coenzyme A (HMG-CoA) reductase. HMG-CoA reductase catalyzes the...
TNU0864 HUP30 312747-21-0 99.8%
HUP30
HUP30 is a potent vasodilating agent. HUP30 can stimulate soluble guanylyl cyclase, activate K+ channels, and block extracellular Ca2+ influx.
T24799 SKA-111 1369170-24-0 99.79%
SKA-111
SKA-111 is a selective calcium-activated potassium phannel (potassium phannel ) KCa3.1 activator that induces membrane hyperpolarization in porcine endothelial c...
ML365
T4316
ML365 is a novel selective small molecule inhibitor of TASK1(KCNK3).
CHET3
T72066
CHET3 is a TASK-3 inhibitor that can be used to study pain.
Dronedarone hydrochloride
T1073
Dronedarone hydrochloride (SR33589) is an amiodarone analog which has an effective and promising treatment for Atrial fibrillation.
GW 542573X
T22826
GW 542573X is a potent and selective small molecule Ca2+-activated K+ 2 (SK2) channel activator.GW 542573X induces a leftward shift in the Ca2+ response curve of...
Loureirin B
T3876
Loureirin B can downregulate the expression of fibrosis-related molecules by regulating MMPs and TIMPs levels, inhibit scar fibroblast proliferation and suppress...
Levcromakalim
TQ0150
Levcromakalim (BRL 38227) is an activator of the ATP-sensitive K+ channel.
Daurisoline
T3054
Daurisoline ((R,R)-Daurisoline) is a hERG inhibitor. Daurisoline is also an autophagy blocker.
VU591
T13320L
1222810-74-3
DCEBIO
T10977
DCEBIO stimulates the secretion of Cl- through the activation of the hIK1 K + channel and the activation of the apical Cl- conductance. DCEBIO is a derivative of...
Prazosin hydrochloride
T1050
Prazosin hydrochloride (Vasoflex) reduces peripheral resistance and relaxes vascular smooth muscles as a selective adrenergic alpha-1 antagonist by a mechanism n...
KT-362 fumarate
T27753
KT-362 fumarate is a novel compound that acts as an antagonist of calcium channels, potassium channels and sodium channels.KT-362 fumarate causes vasodilation by...
O-Nornuciferine
TN1092
O-Nornuciferine reveals distinct in vitro hERG blockages measured in HEK293 cells with the IC50 value of 2.89 uM.
Guanfu base A
T8182
Guanfu base A is a potent noncompetitive CYP2D6 inhibitor (Ki: 1.20 μM in HLMs; Ki: 0.37 μM for rCYP2D6). It also inhibits HERG channel current.
SKF-96365 hydrochloride
T2170
SKF-96365 hydrochloride (SKF96365) , a SOCE inhibitor, exhibits potent anti-neoplastic activity by inducing cell-cycle arrest and apoptosis in colorectal Y cells...
NS8593 hydrochloride
T12256
NS8593 hydrochloride (NS8593 HCl) is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels) .
Endoxifen (Z-isomer)
T2280
Endoxifen Z-isomer (EDX) is a key active metabolite of tamoxifen (TAM) with higher affinity and specificity to estrogen receptors that also inhibits aromatase ac...
ML133 hydrochloride
T6592
ML133 hydrochloride (ML133 HCl) is a selective potassium channel inhibitor for Kir2.1 with IC50 of 1.8 μM (pH 7.4) and 290 nM (pH 8.5), has no effect on Kir1.1 a...
Rosuvastatin
T1676
Rosuvastatin (ZD 4522) is an antilipemic agent that competitively inhibits hydroxymethyl-glutaryl-coenzyme A (HMG-CoA) reductase. HMG-CoA reductase catalyzes the...
HUP30
TNU0864
HUP30 is a potent vasodilating agent. HUP30 can stimulate soluble guanylyl cyclase, activate K+ channels, and block extracellular Ca2+ influx.
SKA-111
T24799
SKA-111 is a selective calcium-activated potassium phannel (potassium phannel ) KCa3.1 activator that induces membrane hyperpolarization in porcine endothelial c...
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15
TargetMol