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Cat. No. Product Name Information
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.
PC-45579

PF-04418948

EP2 antagonist

PF-04418948 (PF 04418948) is a novel potent and selective prostaglandin EP2 receptor antagonist.
PC-45077

Grapiprant

EP4 antagonist

Grapiprant (CJ-023423, AAT-007) is a potent, selective EP4 receptor antagonist with Ki values of 13/20 nM against human and rat EP(4) receptors.
PC-42573

MK-2894 sodium

EP4 antagonist

MK-2894 sodium is a highly potent, selective, second generation prostaglandin E2 subtype 4 receptor (EP4) antagonist with Ki of 0.56 nM.
PC-42572

MK-2894

EP4 antagonist

MK-2894 (MK2894) is a highly potent, selective, second generation prostaglandin E2 subtype 4 receptor (EP4) antagonist with Ki of 0.56 nM.
PC-27072

Evatanepag

EP2 receptor agonist

Evatanepag (CP-533536, CP-533,536) is a highly selective and potent functional EP2 receptor agonist with high affinity to rat EP2 receptor (IC50=50 nM), is >50-fold more selective over EP4 receptor subtype.
PC-27006

TP-18

EP2/EP4 antagonist

TP-18 is a potent, selective, orally available dual PGE2 receptor EP2/EP4 antagonist with IC50 of 9.5/3.3 nM respectively.
PC-26606

SC-51089

EP1 antagonist

SC-51089 (SC51089) is a selective antagonist of prostaglandin E2 EP1 receptor, with Ki values of 1.3, 11.2, 17.5, and 61.1 μM for EP1, TP, EP3, and FP receptors, respectively, exhibits neuroprotective activity.
PC-26564

BPN-37440

EP2 antagonist

BPN-37440 is a potent, selective prostaglandin-E2 receptor EP2 antagonist with IC50 of 53 nM, with no activity against DP1, EP4 and IP receptors.

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