Home   >  
Ion Channel/Membrane Transporter
Potassium Channel

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products






Raw Materials

Potassium Channel

Chemical Structure Cat. No. Product Name CAS No.
MK-7145 Chemical Structure
BCP38355 MK-7145 1255204-84-2
MK-7145 is a ROMK inhibitor, with an IC50 of 0.045 μM.
Flupirtine Chemical Structure
BCP38233 Flupirtine 56995-20-1
Flupirtine is a selective neuronal potassium channel opener act as an Analgesic, having substituted pyridine with central analgesic properties.
ICA-105574 Chemical Structure
BCP38017 ICA-105574 316146-57-3
ICA-105574 is a potent and efficacious hERG channel activator steeply potentiates current amplitudes more than 10-fold with EC50 of 0.5 uM.
OR-1855 Chemical Structure
BCP37945 OR-1855 101328-85-2
OR-1855 belongs to the class of organic compounds known as aniline and substituted anilines.
Kv2-IN-A1 Chemical Structure
BCP37858 Kv2-IN-A1 689297-68-5
Kv2-IN-A1 is a Kv2.1 and Kv2.2 inhibitor.
BMS-191011 Chemical Structure
BCP37808 BMS-191011 202821-81-6
BMS-191011 is an opener of the large-conductance, Ca2+-activated potassium (maxi-K) channel, effective in stroke models.
ML418 Chemical Structure
BCP37608 ML418 1928763-08-9
ML418 is the first potent, selective and CNS penetrating blocker of Kir7.1 potassium channel (IC50, 310 nM), which also potently inhibits Kir6.2/SUR1, and exhibits superior selectivity over other Kir channels.
JNJ303 Chemical Structure
BCP37605 JNJ303 878489-28-2
JNJ 303 has been found to be a potent IKs blocker (IC50 = 64 nM) as well as a 11β-HSD1 inhibitor.
Procainamide Chemical Structure
BCP35189 Procainamide 51-06-9
Procainamide is an oral antiarrhythmic agent that has been in use for more than 60 years. Long term procainamide therapy is known to induce hypersensitivity reactions, autoantibody formation and a lupus-like syndrome but is a rare cause of clinically apparent acute liver injury.
Amiodarone Chemical Structure
BCP35085 Amiodarone 1951-25-3
Amiodarone is an antiarrhythmic drug for inhibition of ATP-sensitive potassium channel with an IC50 of 19.1 μM.
123下一頁末頁共 100 條記錄 1 / 10 頁