| Cat. No. |
Product Name |
Information |
| PC-72122 |
tatM2NX
TRPM2 antagonist
|
tatM2NX is a novel potent, selective, cell permeable, peptide TRPM2 channel antagonist with IC50 of 396 nM, IC90 of 2 uM (TRPM2 channel currents), prevents ligand binding and TRPM2 activation. |
| PC-72111 |
KPR-5714
TRPM8 antagonist
|
KPR-5714 (KPR5714) is a novel potent, selective TRPM8 antagonist with IC50 of 25.3 and 22.4 nM against hTRPM8 and rTRPM8, respectively. |
| PC-72043 |
ML-SA5
Mucolipin 1 agonist
|
ML-SA5 (Mucolipin 1 agonist ML-SA5) is a potent, small molecule agonist of transient receptor potential mucolipin 1 (TRPML1/MCOLN1/ML1), dose-dependently activated whole-endolysosomal ML1 currents in DMD myoblasts with EC50 of 285±144 nM. |
| PC-35928 |
GSK1702934A
TRPC3/6 activator
|
GSK1702934A (GSK-1702934A) is a potent and selective TRPC3/6 activator with EC50 of 80/440 nM, respectively. |
| PC-35713 |
GSK3395879
TRPV4 inhibitor
|
GSK3395879 (GSK-3395879) is a novel potent, selective, orally bioavailable antagonist of TRPV4 with IC50 of 1 nM (hTRPV4). |
| PC-35612 |
AMG333
TRPM8 antagonist
|
AMG333 (AMG-333) is a potent, highly selective TRPM8 antagonist with IC50 of 13 nM and 20 nM for hTRPM8 and rTRPM8, respectively. |
| PC-35474 |
TRPM8 antagonist 14
TRPM8 antagonist
|
TRPM8 antagonist 14 is a potent, selective TRPM8 antagonist with IC50 of 0.2 nM in calcium influx assays, shows no activity on TRPV1. |
| PC-35235 |
AS1928370
TRPV1 inhibitor
|
AS1928370 (ASP8370) is a potent, selective, orally available TRPV1 antagonist with IC50 of 0.51 uM, shows no inhibitory effects on TRPV4, TRPA11, and TRPM8 at 10 uM. |
| PC-35234 |
TRPM4 inhibitor 5
TRPM4 inhibitor, TMEM206 inhibitor
|
TRPM4 inhibitor 5 (TMEM206 inhibitor CBA) is a potent and selective inhibitor of TRPM4 with IC50 of 1.5 uM (Na+ influx), also inhibits TMEM206 with IC50 of 9.55 uM. |
| PC-35045 |
DS88790512 hydrochloride
TRPC6 inhibitor
|
DS88790512 is a potent, selective, and orally bioavailable TRPC6 blocker with IC50 of 11 nM, exhibits excellent selectivity against hERG and hNaV1.5 channels (IC50 >100 uM). |
| PC-35044 |
DS88790512
TRPC6 inhibitor
|
DS88790512 is a potent, selective, and orally bioavailable TRPC6 blocker with IC50 of 11 nM, exhibits excellent selectivity against hERG and hNaV1.5 channels (IC50 >100 uM). |
| PC-63428 |
JNJ-38893777
TRPV1 inhibitor
|
JNJ-38893777 is a potent and selective transient receptor potential vanilloid 1 (TRPV1) channel antagonist for treatment of ociceptive and neuropathic pain. |
