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Cat. No. Product Name Information
PC-60320

AZ-8838

PAR2 inhibitor

AZ-8838 (AZ8838) is a potent, and selective PAR2 antagonist with Kd of 125 nM.
PC-60319

GB-110

PAR2 agonist

GB-110 is a potent, non-peptidic agonist of PAR2 that selectively induces PAR2-mediated intracellular Ca(2+) release in HT29 cells with EC50 of 0.28 uM.
PC-60318

GB-88

PAR2 inhibitor

GB-88 is a selective, orally available PAR2 antagonist that inhibits PAR2 activated Ca(2+) release with IC50 of 2 uM.
PC-42330

Vorapaxar

PAR1 antagonist

Vorapaxar (SCH 530348) is a potent, selective and orally active thrombin receptor PAR-1 antagonist with Ki of 8.1 nM.
PC-47484

TRAP-6

PAR1 agonist

TRAP-6 is a PAR1 peptide fragment (residues 42-47) that acts as a protease activating receptor 1 (PAR1) agonist, stimulates platelet aggregation (EC50=0.8 uM).
PC-21812

PAR4 antagonist 48

PAR4 antagonist

PAR4 antagonist 48 is a potent and selective quinoxaline-based PAR4 antagonist with IC50 of 1.8 nM in FLIPR calcium mobilization assays, inhibits calcium mobilization in human platelet-rich plasma (PRP) aggregation assay with γ-thrombin with IC50 of 2.1 nM.
PC-21762

1-Piperidine Propionic Acid

PAR2 inhibitor

1-Piperidine Propionic Acid (1-PPA) is an allosteric Inhibitor of protease activated receptor-2 (PAR2) with IC50 of 2.3 uM.
PC-20882

PAR2 antagonist C781

PAR2 antagonist

PAR2 antagonist C781 is a potent β-Arrestin biased protease-activated receptor-2 (PAR2) antagonist, effectively reduces 2AT, trypsin and elastase-induced signalling in vitro physiological assays.
PC-20579

AYPGKF-NH2

PAR4 agonist

AYPGKF-NH2 is a potent, PAR4-selective agonist peptide, stimulates platelet aggregation in vitro with EC50 of 15 uM.
PC-20578

TFLLRN-NH2

PAR1 agonist

TFLLRN-NH2 is a potent, PAR1-selective agonist peptide with EC50 of 1.9 uM.
PC-20577

RWJ-58259

PAR1 antagonist

RWJ-58259 (RWJ58259) is a potent, selective thrombin receptor PAR-1 antagonist with binding IC50 of 0.15 uM, and IC50 of 0.07 uM in RASMC calcium mobilization assays.

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