| Cat. No. |
Product Name |
Information |
| PC-43293 |
Dinoprost tromethamine salt
|
Dinoprost (Prostaglandin F2α, PGF2α) is a naturally occurring prostaglandin used to induce labor and as an abortifacient, causes contraction of vascular, bronchial, intestinal, and myometrial smooth muscle, and also exhibits potent luteolytic activity.. |
| PC-43292 |
Dinoprost
|
Dinoprost (Prostaglandin F2α, PGF2α) is a naturally occurring prostaglandin used to induce labor and as an abortifacient, causes contraction of vascular, bronchial, intestinal, and myometrial smooth muscle, and also exhibits potent luteolytic activity.. |
| PC-63165 |
ONO-8055
|
ONO-8055 is a highly selective and potent EP2/EP3 dual agonist with EC50 of 0.67/0.7 nM, shows >450-fold selectivity over EP4 receptors (EC50=339 nM). |
| PC-63012 |
MF266-1
|
MF266-1 is a potent, selective prostaglandin E receptor subtype 1 (EP1) antagonist with Ki of 3.8 nM, displayes a relatively good selectivity over other prostanoid receptors.. |
| PC-63011 |
MF266-3
|
MF266-3 is a potent, selective prostaglandin E receptor subtype 3 (EP3) antagonist with Ki of 0.8 nM. |
| PC-62029 |
TG4-155
|
TG4-155 is a potent and selective prostaglandin EP2 receptor antagonist with Kb of 2.4 nM. |
| PC-61577 |
AM432 sodium
|
AM 432 is potent, selective, orally active prostaglandin D2 receptor (DP2/CRTH2) antagonist with binding IC50 of 6 nM for hDP2. |
| PC-61566 |
ARRY-502
|
ARRY-502 is an orally bioavailable, potent and selective antagonist of the prostaglandin D2 receptor (CRTh2) for treatment of mild to moderate Th2-driven asthma.. |
| PC-61564 |
TASP0376377
|
TASP0376377 is a potent, selective prostaglandin D2 receptor (CRTH2) antagonist with binding IC50 of 19 nM. |
| PC-61555 |
ER-819762
|
ER-819762 is a novel potent, selective, orally active EP4 receptor antagonist with IC50 of 59 nM in cAMP-dependent reporter assay. |
| PC-61499 |
AAT-008
|
A novel potent, and selective prostaglandin EP4 receptor antagonist with binding IC50 of 2.4 nM. |
| PC-60722 |
BMY 45778
|
A potent, non-prostanoid prostacyclin partial agonist that potently inhibits human (IC50=35 nM), rabbit (IC50=136 nM) and rat (IC50=1.3 uM) platelet aggregation. |
