| Cat. No. |
Product Name |
Information |
| PC-60979 |
AMG1
CRAC channel inhibitor
|
AMG1 is a specific CRAC channel inhibitor that blocks function of effector but not regulatory T cells in vitro and attenuates the pogression and severity of EAE in vivo. |
| PC-60883 |
Thapsigargin
SERCA inhibitor
|
Thapsigargin (G202) is a potent, selective, non-competitive inhibitor of the sarco/endoplasmic reticulum Ca2+ ATPase (SERCA), causes ER stress and induces autophagy in mammalian cells. |
| PC-60679 |
TROX-1
|
TROX-1 is a potent, state-dependent blocker of Cav2 channels that preferentially inhibits potassium-triggered calcium influx through recombinant Cav2.2 under depolarized conditions with IC50 of 0.27 uM, compared with hyperpolarized conditions (IC50>20 uM). |
| PC-70096 |
GSK-7975A
CRAC channel blocker
|
GSK-7975A (GSK7975A) is a selective CRAC channel blocker that inhibits store-operated Ca(2+) entry (SOCE) with IC50 of 3.4 uM. |
| PC-60006 |
A-1048400
Calcium channel inhibitor
|
A-1048400 is a potent, selective, orally active N-type and T-type calcium channel blocker with IC50 of 1.4 and 1.2 uM, respectively. |
| PC-45686 |
ABT-639
T-type calcium channel inhibitor
|
ABT-639 is a novel, peripherally acting, selective T-type calcium channel blocker, blocks recombinant human Cav 3.2 in a voltage-dependent fashion (IC50=2 uM). |
| PC-45854 |
NNC 55-0396
T-type calcium channel inhibitor
|
NNC 55-0396 is a potent and selective T-type calcium channel antagonist that blocks recombinant alpha(1)G T-type channels in human embryonic kidney 293 cellswith IC50 of 7 uM. |
| PC-42314 |
MK-8998
T-type calcium channel inhibitor
|
MK-8998 (Suvecaltamide, CX-8998) is a potent and selective antagonist of the T-type calcium channel for the treatment of schizophrenia. |
| PC-42385 |
NS-638
Sodium channel inhibitor
|
NS-638 is a nonpeptide calcium channel blocker that dose dependently inhibits AMPA-stimulated [3H]GABA-release from cultured cortical neurons with IC50 of 4.3 uM. |
| PC-23295 |
Dicoumarol
VRAC inhibitor
|
Dicoumarol (Dicumarol) is an inhibitor of both NAD(P)H:quinone oxidoreductase 1 (NQO1) and PDK1 with IC50 of 0.37 and 19.42 uM respectively, also is a potent VRAC inhibitor. |
| PC-23294 |
SN-89B
LRRC8 inhibitor
|
SN-89B is a potent LRRC8 channel inhibitorsuppresses agonist-induced platelet activation and aggregation (IC50=840 nM). |
| PC-23293 |
SN-407
LRRC8 inhibitor
|
SN-407 is a potent VRAC inhibitor with IC50 of 1.6 uM in HEK cells, targets LRRC8 complex and blocks agonist-induced aggregation, ATP release, and calcium influx in platelets. |
