| Cat. No. |
Product Name |
Information |
| 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. |
| PC-60839 |
RPR260243
hERG activator
|
RPR260243 is a potent, selective hERG potassium channel (Kv11.1) activator that dramatically slows current deactivation at 1-30 uM. |
| PC-60838 |
SKF-32802
hERG activator
|
SKF-32802 is a potent, selective hERG potassium channel (Kv11.1) activator that induces a leftward shift in the voltage dependence of activation. |
| PC-60837 |
BeKm-1
hERG inhibitor
|
BeKm-1 is a potent, selective peptide inhibitor of hERG channel with IC50 of 3.3 nM for hERG1 channels. |
| PC-60836 |
AZSMO-23
hERG activator
|
AZSMO-23 (AZSMO 23, AZSMO23) is a potent hERG potassium channel (Kv11.1) activator that activates WT hERG pre-pulse and tail current with EC50 of 28.6 and 11.2 μM respectively. |
| PC-60835 |
ML-T531
hERG activator
|
ML-T531 (CFK332-B) is a potent, selective hERG potassium channel (Kv11.1) activator with EC50 of 3.13 uM. |
| PC-60834 |
PD-307243
hERG activator
|
A potent hERG channel activator that concentration-dependently increases the hERG current (2.1 and 3.4-fold at 3 and 10 uM, respectively) and markedly slows hERG channel deactivation and inactivation. |
