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Cat. No. Product Name Information
PC-28235

DT-9081

EP4 antagonist

DT-9081 is a potent, selective and orally bioavailable antagonist of prostaglandin E2 receptor EP4 (EP4R), counteracts tumor-driven immunosuppression.
PC-28214

KF-0210

EP4 antagonist

KF-0210 is a potent, selective and oral EP4 receptor antagonist with binding IC50 of 18.6 nM, shows >500-fold selectivity over other prostaglandin receptors, including EP1, EP2, EP3, IP, DP1, and FP.
PC-27721

GR63799

EP3 agonist

GR63799X (GR63799) is a potent and selective prostanoid EP3 receptor agonist.
PC-27720

DG041

EP3 antagonist

DG-041 (DG041) is a potent and selective prostanoid EP3 receptor antagonist with IC50 of 4.6 nM and 8.1 nM in binding and FLIPR assay, respectively.
PC-27537

HTL0039732

EP4 antagonist

HTL0039732 is a potent, selective and orally bioavailable E-type prostanoid receptor 4 (EP4) antagonist, blocks signalling through prostaglandin E2 receptor EP4, enhances immune response against tumours that typically resist current immunotherapies.
PC-24436

ACT-1002-4271

EP2/EP4 antagonist

ACT-1002-4271 is a potent, selective dual EP2/EP4 antagonist with IC50 of 6 nM/3 nM for hEP2/hEP4 respectively in cAMP-based activity assays.
PC-35836A

PGN 9856-isopropyl ester

EP2 receptor agonist

PGN 9856-isopropyl ester is the isopropyl ester, which is a potent, selective prostaglandin EP2 receptor agonist with pKi of > 8.3.
PC-35836D

d4-PGN9856

EP2 receptor agonist

d4-PGN9856 is a d4-labelled PGN-9856, which is a potent, selective prostaglandin EP2 receptor agonist.
PC-21314

AZD1981

DP2 (CRTh2) inhibitor

AZD1981 is a potent and selective CRTh2 (DP2) antagonist with pIC50 of 8.4 (human recombinant DP2), with no significant affinity towards recombinant human DP1 receptors.
PC-20915

Selexipag

IP receptor agonist

Selexipag (NS-304) is an orally available, long-acting nonprostanoid prostacyclin receptor (IP receptor) agonist, the prodrug of the active form of MRE-269.
PC-20856

LY3127760

EP4 antagonist

LY3127760 is a potent, selective prostaglandin E4 (EP4) receptor antagonist with binding Ki of 58 nM (hEP4) and cAMP IC50 of 5.6 nM.
PC-20854

CR6086

EP4 antagonist

CR6086 (Vorbipiprant) is a potent, selective prostaglandin E2 receptor 4 (EP4) antagonist with Ki of 16.6 nM (hEP4 receptor), inhibits PGE2-stimulated cAMP production with IC50 of 22 nM.

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