| Cat. No. |
Product Name |
Information |
| PC-21579 |
HC-030031
TRPA1 inhibitor
|
HC-030031 is a potent, selective TRPA1 inhibitor, inhibits AITC- and formalin-evoked calcium influx with IC50s of 6.2 and 5.3 μM, respectively. |
| PC-21130 |
VPC01091.4
TRPM7 inhibitor
|
VPC01091.4 is a non-phosphorylatable FTY720 analogue and novel TRPM7 inhibitor, inhibits IM7 in a dose-dependent manner with IC50 of 0.665 uM. |
| PC-20875 |
TRPV2 inhibitor IV2-1
TRPV2 inhibitor
|
TRPV2 inhibitor IV2-1 is a novel TRPV2-selective blocker, inhibits 2-APB elicited typical inwardly rectifying TRPV2 currents with IC50 of 0.8 uM. |
| PC-20743 |
SAR7334
TRPC6 inhibitor
|
SAR7334 (SAR-7334 ) is a highly potent and selective inhibitor of TRPC6 channel, reduces TRPC6-mediated Ca2+ influx with IC50 of 9.5 nM. |
| PC-20552 |
GsMTx4
TRPC1/6 inhibitor
|
GsMTx4 is a spider venom peptide that selectively inhibits cationic mechanosensitive channels (MSCs) such as TRPC1 and TRPC6 and Piezo channels, also blocks cation-selective stretch-activated channels (SACs). |
| PC-20367 |
TRPM5 inhibitor NDNA
TRPM5 inhibitor
|
TRPM5 inhibitor NDNA is potent and selecive TRPM5 inhibitor, inhibits Ca2+- induced TRPM5 currents with IC50 of 2.4 nM. |
| PC-20366 |
Triphenylphosphine oxide
TRPM5 inhibitor
|
Triphenylphosphine oxide (TPPO) is a selective and potent inhibitor of TRPM5 with IC50 of 12 and 30 uM for human and murine TRPM5 heterologously expressed in HEK293 cells. |
| PC-49702 |
AZ465
TRPA1 inhibitor
|
AZ465 (AZ-465) is a potent selective TRPA1 inhibitor, potently inhibitor Zn2+ (100 μM)- and O-chlorobenzylidene malononitrile (CS) (10 nM)-induced TRPA1 activation with IC50 of 85 nM and 20 nM, respectively. |
| PC-49701 |
AMG2504
TRPA1 inhibitor
|
AMG2504 (AMG 2504) is a selective small molecule TRPA1 inhibitor, inhibits AITC-induced increase in intracellular calcium mediated by TRPA1 in CHO cells with IC50 of 35 nM. |
| PC-49700 |
GRC-17536
TRPA1 inhibitor
|
GRC-17536 (GRC 17536) is a potent and selective TRPA1 antagonist, inhibits citric acid -induced Ca+2 influx with IC50 of 8.2 nM in cell-based assays. |
| PC-49696 |
BAY-390
TRPA1 inhibitor
|
BAY-390 (BAY390) is a potent, selective, brain-penetrant TRPA1 inhibitor with IC50 of 16 and 63 nM for hTRPA1 and rTRPV1, respectively. |
| PC-49684 |
JT010
TRPA1 agonist
|
JT010 (JT-010) is a potent, site-selective and covalent TRPA1 agonist, opens the TRPA1 channel by covalently and site-selectively binding to Cys621 with EC50 of 0.65 nM. |
