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Potassium Channel Potassium channel

Cat.No.  Name Information
M4973 BAPTA-AM BAPTA-AM is a selective, membrane-permeable calcium chelator. BAPTA-AM inhibits hERG channels, hKv1.3 and hKv1.5 channels in HEK 293 cells with IC50s of 1.3 μM, 1.45 μM and 1.23 μM, respectively.
M2181 ML133 hydrochloride ML133 hydrochloride is a selective inhibitor of the Kir2 family of inward rectifier (IRK, KCNJ) potassium channels.
M3456 Chlorpromazine hydrochloride Chlorpromazine hydrochloride is an antagonist of D2, 5HT2A, potassium and sodium channels. The Ki of Chlorpromazine Hydrochloride to D2 and 5HT2A were 363 nM and 8.3 nM, respectively. Chlorpromazine also excites the 20S proteasome. *The compound is unstable in solutions, freshly prepared is recommended
M7029 Nigericin sodium salt Nigericin (NSC 292567) sodium salt is a selective K+ ionophore, Nigericin sodium salt is also an NLRP3 activator which can activate NLRP3 inflammasome to induce pro-inflammatory and immunostimulatory processes.
M52729 Vm24-toxin Vm24-toxin is a toxin peptide that can be isolated from the Mexican scorpion Vaejovis mexicanus smithy.
M52728 ShK toxin ShK toxin blocks voltage-dependent potassium channel (Kv1.3 channel).
M52727 PE 22-28 PE 22-28 is a TREK-1 inhibitor with IC50 value of 0.12 nM.
M52726 Spinoxin Spinoxin isolated from the venom of scorpion Heterometrus spinifer, is a 34-residue peptide neurotoxin cross-linked by four disulfide bridges.
M52725 HsTX1 HsTX1, from the scorpion Heterometrus spinnifer, is a 34-residue, C-terminally amidated peptide cross-linked by four disulfide bridges.
M49431 Dendrotoxin K TFA Dendrotoxin K TFA is a Kv1.1 channel blocker that controls the release of glutamate from presynaptic spike waves into CA3 neurons in a time-dependent manner.
M43879 Isopropyl unoprostone UF-021, an analog of a prostaglandin metabolite and activator of large conductance calcium-activated potassium channels (BK channels), lowers intraocular pressure (IOP) by increasing aqueous humor outflow, and may be used in studies related to glaucoma.
M42246 PD-307243 PD-307243 is a hERG channel activator.
M42245 Kv3 modulator 5 Kv3 modulator 5 is a Kv3 channel modulator.
M42244 Clobutinol hydrochloride Clobutinol hydrochloride is a compound that has anti-tussive effects.
M42243 ZM226600 ZM226600 is an ATP-sensitive potassium channel opener (EC50: 500 nM).
M42242 Tamapin TFA Tamapin TFA is a venom peptide, targeting to small conductance Ca(2+)-activated K(+) (SK) channels.
M42241 AmmTX3 AmmTX3 is a peptide toxin that can be isolated from the venom of the scorpion Androctonus mauretanicus.
M42240 BDS-I BDS-I known as blood depressing substance, is a marine toxin which can be extracted from Anemonia sulcata.
M42239 VU590 dihydrochloride VU590 dihydrochloride is a potent and moderately selective ROMK (Kir1.1) inhibitor, with an IC50 of 290 nM.
M42238 KV1.3-IN-1 KV1.3-IN-1 is a KV1.3 channel inhibitor (IC50: 230 nM and 26.12 nM in Ltk cells and PHA-activated T-lymphocytes respectively).
M42237 SKA-111 SKA-111 is a selective activator of potassium phannel KCa 3.1 , evokes KCa 3.1 membrane hyperpolarization in porcine endothelial cell.
M42236 BmP02 BmP02 is a selective Kv1.3 channel blocker and a highly-selective Kv4.2 modulator, which can be isolated from Chinese scorpion (Buthus martensi Karsch) venom.
M42235 Budiodarone tartrate Budiodarone (ATI-2042) tartrate is a chemical analogue of Amiodarone with balanced, multiple cardiac ion channel (potassium, sodium and calcium channels) inhibiting activity.
M41127 Quinine sulfate hydrate Quinine sulfate hydrate (2:1:4) is an orally active potassium channel inhibitor that inhibits voltage pulse-induced currents in MT mSlo3 (KCa5.1) channels +100 mV with an IC50 of 169 μM.In addition, Quinine sulfate hydrate binds to PfPNP with low nanomolar affinity. In addition, Quinine sulfatehydrate binds to purine nucleoside phosphorylase (PfPNP) with low nanomolar affinity.




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