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首页-小分子抑制剂&激动剂-GPCR-Prostaglandin Receptor

Request The Product List ofProstaglandin Receptor Prostaglandin Receptor

Cat. No. Product Name Information
PC-70016

AH-23848 calcium salt

TP1/EP4 antagonist

AH-23848 calcium salt is a dual antagonist of TP1 and EP4 receptors that inhibit TXA2-induced platelet aggregation with IC50 of 0.26 uM.
PC-42574

AH6809

PGD2 antagonist

AH6809 is a xanthone derivative that fuctions as an EP and DP receptor antagonist with Ki of 1217, 1150, 1597, and 1415 nM for the cloned human EP1, EP2, EP3-III, and DP receptor respectively.
PC-45075

Fevipiprant

CRTH2 inhibitor

Fevipiprant (NVP-QAW039, QAW-039) is a potent, selective, slowly dissociating CRTh2 antagonist with Kd of 1.14 nM.
PC-42700

CJ-042794

EP4 antagonist

CJ-042794 (CJ-42794) is a potent, selective prostaglandin E receptor subtype 4 (EP4) antagonist with pKi of 8.5.
PC-42699

MF498

EP4 antagonist

MF498 is a selective prostaglandin E receptor subtype 4 (EP4) antagonist with Ki of 0.74 nM.
PC-46004

MRE-269

IP receptor inhibitor

MRE-269 (ACT-333679) is a potent, selective IP receptor (prostaglandin I2 receptor) agonist with Ki of 20 nM.
PC-45896

ONO-AE3-208

EP4 antagonist

ONO-AE3-208 (AE3-208) is a potent, selective EP4 receptor antagonist with Ki of 1.3 nM.
PC-45118

Terutroban

Prostanoid TP receptor antagonist

Terutroban (S-18886) is a potent, selective antagonist of the thromboxane receptor (Prostanoid TP receptor) that blocks thromboxane induced platelet aggregation and vasoconstriction.
PC-42387

PGD2-IN-1

PGD2 antagonist

PGD2-IN-1 is a potent prostaglandin D2 receptor (PGD2, DP) receptor antagonist with IC50 of 0.3 nM.
PC-45826

Laropiprant

DP1 antagonist

Laropiprant (MK-0524) is a potent and selective prostaglandin D2 (PGD2) receptor (DP1) antagonist with Ki of 0.57 nM.
PC-45103

GW627368

EP4 antagonist

GW627368 is a potent and selective competitive antagonist of prostanoid EP4 receptor with pKi of 7.0.
PC-45111

TG6-10-1

EP2 antagonist

TG6-10-1 is a potent and selective antagonist of prostaglandin E2 receptor subtype EP2 with Kb of 17.8 nM.

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