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Cat. No. Product Name Information
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-24012

Latanoprost

FP receptor agonist

Latanoprost (PHXA41) is a prostaglandin F2α analogue and prostaglandin FP receptor agonist, increases uveoscleral outflow of aqueous humor.
PC-24011

Bimatoprost

Prostaglandin FP receptor agonist

Bimatoprost (AGN 192024) is a prostaglandin analog and prostaglandin FP receptor agonist with Ki of 6.3 uM, reduces intraocular pressure by regulating scleral and trabecular outflow.
PC-23531

Seratrodast

TXA2 antagonist, Ferroptosis inhibitor

Seratrodast (AA2414) is a potent, specific thromboxane A2 (TXA2) receptor antagonist, competitively inhibits the contractile response to U-46619 in guinea pig tracheal and parenchymal strips and dog saphenous vein strips with pA2 values of 7.69, 8.29 and 6.79, respectively, also inhibits ferroptosis.
PC-22638

Asapiprant

DP1 antagonist

Asapiprant (S-555739) is a potent and selective prostaglandin DP1 receptor antagonist with Ki of 0.44 nM, >300-fold selective over EP2 and other prostanoid receptors.
PC-22116

Travoprost

FP receptor agonist

Travoprost (Fluprostenol isopropyl ester), an isopropyl ester proagent, is a high affinity, selective FP prostaglandin full receptor agonist with Ki of 52 nM, functional EC50 of 27 nM.
PC-22027

L-902688

EP4 agonist

L-902688 (L-902,688) is a potent, selective and orally active EP4 receptor agonist with Ki of 0.38 nM and EC50 of 0.6 nM, >4,000-fold selective for EP4 over other EP and prostanoid receptors.
PC-21515

EP4R antagonist 77

EP4 antagonist

EP4R antagonist 77 is the sodium salt of EP4R antagonist 74, a potent, selective EP4 receptor antagonist with Ki of 11.2 nM.

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