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Cat. No. Product Name Information
PC-49647

PAR1 inhibitor Q94

PAR1 antagonist

Q94 is a selective PAR1 antagonist and allosteric modulator that selectively block PAR(1) /Gα(q) interaction and signalling.
PC-73008

UDM-001651

PAR4 inhibitor

UDM-001651 (UDM001651) is a potent, selective, and orally bioavailable PAR4 antagonist with IC50 of 2.4 nM.
PC-72283

PAR2 antagonist C391

PAR2 antagonist

PAR2 antagonist C391 (C391) is a selective PAR2 antagonist, potently inhibits peptidomimetic-induced PAR2 Ca2+ signalling with IC50 of 1.3 uM.
PC-38310

I-287

PAR2 inhibitor

I-287 is a potent, selective, orally active inhibitor of PAR2, negative PAR2 allosteric modulator, inhibits PAR2-mediated activation of Gq and G12/13 but not Gi/o proteins (IC50=45-390 nM).
PC-60320A

AZ8838 racemate

PAR2 inhibitor

AZ8838 racemate (AZ-8838 racemate) is the racemate form of AZ8838, which is a potent, and selective PAR2 antagonist with Kd of 125 nM..
PC-35139

BAY-386

PAR1 antagonist

BAY-386 (BAY386) is a potent, specific and reversible PAR-1 antagonist with IC50 of 10 nM (HEK cell) and binding IC50 of 56 nM, without affinity for PAR-4 (IC50>10 uM).
PC-62640

Parmodulin 2

PAR-1 antagonist

Parmodulin 2 (ML161) is a potent, specific antagonist of PAR-1, specifically inhibits thrombin-tethered ligand (TL) peptide-mediated platelet aggregation with IC50 of 7 uM.
PC-62125

ML354

PAR4 antagonist

ML354 (VU0099704) is a novel potent and selective PAR4 antagonist with IC50 of 140 nM, displays 71-fold selectivity versus PAR-1.
PC-62088

I-191

PAR2 inhibitor

I-191 (I191, I 191) is a novel potent, selective protease-activated receptor 2 (PAR2) antagonist with pIC50 of 7.2 in cell-based assays.
PC-62040

JF-5

PAR1 antagonist

JF5 (PAR1 inhibitor JF5) is an allosteric inhibitor of PAR1 that binds to helix 8 of the receptor.
PC-61618

GB-83

PAR2 inhibitor

GB-83 is a selective, reversible PAR2 (Protease-activated receptor 2) antagonist with IC50 of 2 uM.
PC-61561

ENMD-1068

PAR2 inhibitor

ENMD-1068 is a novel selective PAR2 antagonist without inhibitory activity against thrombin-mediated PAR3 and PAR4 signaling.

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