| Cat. No. |
Product Name |
Information |
| PC-60669 |
RY796
Kv2 inhibitor
|
A novel potent, selective Kv2 channel inhibitor that potently inhibits Kv2.1 and Kv2.2 with IC50 of 0.14 and 0.09 uM, respectively. |
| PC-60655 |
Charybdotoxin
BKCa inhibitor
|
Charybdotoxin (ChTX) selective, potent peptidyl blocker of the big conductance Ca2+-activated K+ channel (BKCa, KCa1.1, MaxiK). |
| PC-60654 |
Iberiotoxin
BKCa inhibitor
|
Iberiotoxin (IbTX) is a selective, potent peptidyl blocker of the big conductance Ca2+-activated K+ channel (BKCa, KCa1.1, MaxiK) with IC50 of 0.25 nM. |
| PC-60653 |
NS19504
BKCa activator
|
A novel selective, small molecule large-conductance Ca(2+)-activated K(+) channel (BKCa, KCa1.1, MaxiK) positive modulator with EC50 of 11 uM. |
| PC-60648 |
AUT2
Kv3 modulator
|
AUT2 is a novel specific, cell permeant modulator of Kv3 channels with EC50 of 0.9 and 1.9 uM for Kv3.1b and Kv3.2a, respectively. |
| PC-60647 |
AUT1
Kv3 modulator
|
AUT1 (AUT-1) is a novel specific, cell permeant modulator of Kv3 channels with EC50 of 4.7 and 4.9 uM for Kv3.1b and Kv3.2a, respectively. |
| PC-60576 |
ML418
Kir7.1 inhibitor
|
ML418 (ML-418) is the first potent, selective, CNS penetrating inward rectifier potassium channel Kir7.1 (KCNJ13) inhibitor with IC50 of 0.31 uM. |
| PC-60575 |
BNBI
ROMK inhibitor
|
BNBI is a selective renal outer medullary potassium channel (ROMK, Kir1.1) inhibitor with IC50 of 8 uM in T1+ flux assays, does not inhibit Kir7.1 at 100 uM. |
| PC-60574 |
VU714 oxalate
Kir7.1 inhibitor
|
VU714 oxalate is a potent inwardly rectifying K+ channel Kir7.1 inhibitor with IC50 of 5.6 uM in T1+ flux assays. |
| PC-60573 |
VU714
Kir7.1 inhibitor
|
VU714 is a potent inwardly rectifying K+ channel Kir7.1 inhibitor with IC50 of 5.6 uM in T1+ flux assays. |
| 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. |
