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Cat. No. Product Name Information
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, also enhances oligodendrocyte formation via HSD17B7 inhibition.
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-27337

TRPV1 agonist MSP20

TRPV1 agonist

MSP20 is a potent, selective TRPV1 agonist with EC50 of 46 nM and Emax=78.24%, shows no agonist activity against TRPV3, TRPV4 and TRPM8 receptors.
PC-27302

TRPV4 antagonist 39

TRPV4 antagonist

TRPV4 antagonist 39 is a potent, selective TRPV4 antagonist with IC50 of 0.2 nM.
PC-27188

9-phenanthrol

TRPM4 inhibitor

9-Phenanthrol (9-Hydroxyphenanthrene) is a specific, reversible small molecule TRPM4 inhibitor with IC50 of 17 uM, is ineffective on the related channel TRPM5.
PC-26841

Ononetin

TRPM3 antagonist

Ononetin is a deoxybenzoin from Ononis spinosa and selective TRPM3 antagonist with IC50 of 0.3 uM.
PC-26530

CMP233

TRPM4 antagonist

CMP233 is a potent, selective TRPM4 channel antagonist with IC50 of 0.15 uM.
PC-26527

TRPM4 inhibitor PBA

TRPM4 inhibitor

TRPM4 inhibitor PBA is a specific small molecule inhibitor of Ca2+-activated monovalent cation channel TRPM4 with IC50 of 339 nM using the fluorescence-based Na+-influx assay on HEK293 cells stably overexpressing hTRPM4.
PC-26459

IMTU

TRPV1 antagonist

IMTU is a potent and selective TRPV1 antagonist with IC50 of 128.34 nM, significantly inhibits the capsaicin-induced calcium influx.

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