Cat. No. |
Product Name |
Information |
PC-42419 |
AMG-9810
TRPV1 inhibitor
|
AMG-9810 is a potent, selective and competitive TRPV1 antagonist with IC50 of 24.5 and 85.6 nM for human and rat TRPV1, respectively. |
PC-45556 |
PF-4840154
TRPA1 agonist
|
PF-4840154 is a potent, selective agonist of the rat (EC50=97 nM) and human (EC50=23 nM) TRPA1 channel. |
PC-42017 |
SKF-96365 hydrochloride
SOCE inhibitor
|
SKF-96365 hydrochloride (SKF96365) is potent inhibitor of receptor-mediated calcium entry (RMCE) with IC50 of 8.5 and 11.7 uM for inhibition in platelets stimulated with ADP and thrombin, respectively. |
PC-42689 |
AMG517
TRPV1 antagonist
|
AMG517 is a potent and selective vanilloid receptor TRPV1 antagonist with IC50 of 0.76 nM for hTRPV |
PC-42931 |
SB-366791
TRPV1 antagonist
|
SB-366791 (SB366791) is a potent and selective vanilloid receptor (VR1/TRPV1) antagonist with IC50 of 5.7 nM. |
PC-42084 |
HC-067047
TRPV4 inhibitor
|
HC-067047 (HC067047) is a potent and selective TRPV4 antagonist with IC50 of 48 nM, 133 nM, and 17 nM for human, rat, and mouse TRPV4 in cell assays, respectively. |
PC-45632 |
Pyr10
TRPC3 inhibitor
|
Pyr10 is a novel TRPC3-selective inhibitor, inhibits Ca2+ influx in carbachol-stimulated TRPC3-transfected HEK293 cells with IC50 of 0.72 uM. |
PC-45764 |
BCTC
TRPV1 antagonist
|
BCTC is a highly potent, selective, CNS-penetrant TRPV1 antagonist that inhibits capsaicin-induced and acid-induced activation of rat TRPV1 with IC50 values of 35 and 6 nM, respectively. |
PC-45355 |
Nonivamide
TRPV1 agonist
|
Nonivamide is a capsaicin analog that acts as an agonist of TRPV1 channel. |
PC-23622 |
LY3526318
TRPA1 antagonist
|
LY3526318 is an orally bioavailable, potent, and selective TRPA1 antagonist with limited penetration to the central nervous system, effectively blocks cinnamaldehyde-evoked activation of rat and human TRPA1. |
PC-23550 |
Pyr3
TRPC3 inhibitor
|
Pyr3 is a potent, selective inhibitor of transient receptor potential canonical channel 3 (TRPC3) with IC50 of 700 nM for inhibition of TRPC3-mediated Ca2+ influx. |
PC-23549 |
TRPC3 antagonist 60a
TRPC3 inhibitor
|
TRPC3 antagonist 60a is a potent, selective RPC3 antagonist with IC50 of 60 nM, has significant neuronal protective abilities. |