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Cat. No. Product Name Information
PC-28517

Carvacrol

TRPV3 agonist

Carvacrol (Cymophenol) is a small molecule agonist / activator of TRPV3 with EC50 of 0.39 uM, also is an inhibitor of Drosophila TRPL and mammalian TRPM7 channels, also causes cell cycle arrest in G0/G1, downregulates Notch-1, and Jagged-1 and induces apoptosis, shows antioxidant, antibacterial, antifungal, anticancer, anti-inflammatory, hepatoprotective, spasmolytic, and vasorelaxant properties.
PC-28515

SAR7334 hydrochloride

TRPC6 inhibitor

SAR7334 hydrochloride (SAR-7334) is a highly potent and selective inhibitor of TRPC6 channel, reduces TRPC6-mediated Ca2+ influx with IC50 of 9.5 nM.
PC-28400

MRTF-A-IN-2

MRTF/SRF inhibitor, TRPM7-RhoA inhibitor

MRTF-A-IN-2 is a potent inhibitor of TRPM7-RhoA interaction, reduces reduced expression of the MRTF/SRF target genes TGF-β1 and TSPAN5, inhibiting cell proliferation and inducing senescence in HCC cells.
PC-28399

MRTF-A-IN-1

MRTF/SRF inhibitor, TRPM7-RhoA inhibitor

MRTF-A-IN-1 is a potent inhibitor of TRPM7-RhoA interaction, reduces reduced expression of the MRTF/SRF target genes TGF-β1 and TSPAN5, inhibiting cell proliferation and inducing senescence in HCC cells.
PC-28383

TRPM8 antagonist Compound 496

TRPM8 antagonist

TRPM8 antagonist Compound 496 is a potent and selective antagonists of TRPM8, potently inhibits menthol and cold-induced increase in intracellular calcium in cells expressing rat TRPM8 with IC50 of 25.8 nM.
PC-28233

Ethylisopropylamiloride

Macropinocytosis inhibitor

Ethylisopropylamiloride (EIPA) is specific macropinocytosis inhibitor that inhibits endocytosis via the macropinocytic pathway, also inhibits TRPP3-mediated Ca2+-activated currents with IC50 of 10.5 uM, inhibits epithelial sodium channels (ENaC) as well as of several other Na+/H+ antiporters.
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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