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Cat. No. Product Name Information
PC-73096

GSK3527497

TRPV4 inhibitor

GSK3527497 (GSK-3527497) is a potent, selective TRPV4 inhibitor with IC50 of 12 nM (hTRPV4).
PC-73026

ML-SI3

TRPML1 antagonist

ML-SI3 (Mucolipin-specific synthetic inhibitor 3) is a synthetic antagonist of transient receptor potential mucolipin 1 (TRPML1), prevents lysosomal calcium efflux and blocks downstream TRPML1-mediated induction of autophagy.
PC-73025

ML-SA1

TRPML1 agonist

ML-SA1 (Mucolipin-specific synthetic agonist 1) is a potent synthetic agonist for TRPML1.
PC-72922

JW-65

TRPC3 inhibitor

JW-65 (JW65) is a selective, potent, CNS-permeable TRPC3 inhibitor improved stability compared to Pyr3.
PC-72671

ML2-SA1

TRPML2 agonist

ML2-SA1 is a potent, selective and efficacious activator (agonist) of TRPML2 with EC50 of 1.24 uM and 2.38 uM for human and mouse TRPML2, respectively.
PC-72599

GSK2798745

TRPV4 inhibitor

GSK2798745 (GSK-2798745) is a potent, selective TRPV4 inhibitor with IC50 of 1.8/1.6 nM (hTRPV4/rTRPV4).
PC-72566

SH045

TRPC6 inhibitor

SH045 (SH-045, Larixyl-6-N-methylcarbamate) is a potent, selective TRPC6 antagonist (blocker) with IC50 of 63 nM.
PC-72565

BI-749327

TRPC6 inhibitor

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-72354

RGM8-51

TRPM8 antagonist

RGM8-51 is a β-lactam derivative, potent, selective TRPM8 antagonist with IC50 of 1.06 and 1.74 uM for rat and human TRPM8, respectively.
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).

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