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Cat. No. Product Name Information
PC-44297

Clopidogrel

P2Y12 antagonist

Clopidogrel (Clopidogrelum) is a thienopyridine-class antiplatelet agent that works by irreversibly inhibiting P2Y12 receptor on platelets.
PC-42218

Ticagrelor

P2Y12 antagonist

Ticagrelor (AZD6140) is a potent, selective, reversible and oral P2Y12 receptor antagonist with pKi of 8.7.
PC-23318

PSB-18422

GPR17 agonist

PSB-18422 is a potent, selective agonist of orphan receptor GPR17 with EC50 of 27.9 nM, selective over human P2Y receptor subtypes.
PC-23316

PSB-24040

GPR17 antagonist

PSB-24040 is a potent antagonist of orphan receptor GPR17 with Ki of 83.2 nM, and pIC50 of 7.48 in calcium mobilization assays.
PC-23315

PSB-22269

GPR17 antagonist

PSB-22269 is a potent antagonist of orphan receptor GPR17 with Ki of 8.91 nM, and pIC50 of 6.9 in calcium mobilization assays.
PC-22687

Vicagrel

P2Y12 antagonist

Vicagrel is a highly potent and orally bioavailable antiplatelet agent, irreversible P2Y12 receptor antagonist.
PC-22477

P2Y2R/GPR17 antagonist 14m

P2Y2R/GPR17 antagonist

P2Y2R/GPR17 antagonist 14m is a potent, dual P2Y2R/GPR17 antagonist with IC50 of 3.17 and 1.67 μM respectively, selective versus other closely related P2Y receptors.
PC-22103

PPTN hydrochloride

P2Y14 antagonist

PPTN hydrochloride is a potent, highly specific antagonist of P2Y14 receptor with Ki of 0.4 nM in functional assays.
PC-22102

PPTN

P2Y14 antagonist

PPTN is a potent, highly specific antagonist of P2Y14 receptor with Ki of 0.4 nM in functional assays.
PC-21206

PSB-0739

P2Y12 antagonist

PSB-0739 is a high potent, non-nucleotide-derived competitive antagonist of platelet P2Y12 receptor with Ki of 24.9 nM.
PC-20994

MRS2768 tetrasodium salt

P2Y2R agonist

MRS2768 is a selective P2Y2 receptor agonist with EC50 of 1.89 uM, shows no effect for human P2Y4 or P2Y6 receptors.
PC-20993

AR-C118925

P2Y2R antagonist

AR-C118925 is a potent, selective, competitive P2Y2 receptor antagonist with pA2 values of 37.2 nM and 51.3 nM in calcium and β-arrestin assays, respectively.

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