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Cat. No. Product Name Information
PC-45556

PF-4840154

TRPA1 agonist

PF-4840154 is a potent, selective agonist of the rat (EC50=97 nM) and human (EC50=23 nM) TRPA1 channel.
PC-42017

SKF-96365 hydrochloride

SOCE inhibitor

SKF-96365 hydrochloride (SKF96365) is potent inhibitor of receptor-mediated calcium entry (RMCE) with IC50 of 8.5 and 11.7 uM for inhibition in platelets stimulated with ADP and thrombin, respectively.
PC-42689

AMG517

TRPV1 antagonist

AMG517 is a potent and selective vanilloid receptor TRPV1 antagonist with IC50 of 0.76 nM for hTRPV
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.
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-23230

Plumbagin

TRPV2 inhibitor

Plumbagin (2-Methyljuglone) is a naphthoquinone isolated from Plumbago zeylanica, exhibits anticancer and antiproliferative activities, also is a potent TRPV2 negative allosteric modulator with IC50 of 0.85 μM, exhibiting >14-fold selectivity over TRPV1, TRPV3 and TRPV4.
PC-22981

Capsazepine

TRPV1 antagonist

Capsazepine is a selective antagonist of vanilloid receptor TRPV1 with IC50 of 562 nM.
PC-22742

GSK3491943

TRPV4 inhibitor

GSK3491943 is a potent, selective TRPV4 inhibitor with IC50 of 3.2 nM (hTRPV4).
PC-22421

TRPV1 antagonist CX-3

TRPV1 antagonist

TRPV1 antagonist CX-3 is a first-in-class highly selective TRPV1 antagonist with IC50 of 26.2 nM, inhibits TRPV1 current with IC50 value of 9.71 uM in whole-cell patch-clamp assay.

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