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Cat. No. Product Name Information
PC-72565

BI-749327

TRPC6 blocker

BI-749327 (BI 749327) is a potent, selective orally bioavailable TRPC6 antagonist (blocker) with IC50 of 13/19/15 nM for mouse/human/guinea pig TRPC6, respectively.
PC-72460

GDC-0334

TRPA1 antagonist

GDC-0334 (GDC0334) is a highly potent, selective, orally bioavailable TRPA1 antagonist with IC50 of 1.7 nM in cell-based assays.
PC-72125

JNJ-28583113

TRPM2 antagonist

JNJ-28583113 (JNJ28583113) is a potent, selective, brain penetrant TRPM2 antagonist with IC50 of 126 nM (hTRPM2).
PC-72123

AM237

TRPC5 activator

AM237 is a selective TRPC5 channel activator that potently activated homomeric TRPC5:C5 channels (EC50=15–20 nM in Ca2+i assays).
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-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-35044

DS88790512

TRPC6 blocker

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-43289

ML204 hydrochloride

TRPC4/TRPC5 inhibitor

ML204 hydrochloride is a potent, selective antagonist of TRPC4 and TRPC5 channels, inhibits TRPC4β-mediated intracellular Ca(2+) rise with IC50 of 0.96 uM, exhibits 19-fold selectivity against TRPC6 channel.
PC-43288

ML204

TRPC4/TRPC5 inhibitor

ML204 is a potent, selective antagonist of TRPC4 and TRPC5 channels, inhibits TRPC4β-mediated intracellular Ca(2+) rise with IC50 of 0.96 uM, exhibits 19-fold selectivity against TRPC6 channel.

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