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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1626 | Prostaglandin E1 | PGE1,Alprostadil | Endogenous Metabolite , Prostaglandin Receptor |
Prostaglandin E1 (Alprostadil) is the naturally occurring prostaglandin E1 (PGE1) which displays a variety of pharmacologic actions. Prostaglandin E1 is a potent vasodilator agent that increases peripheral blood flow, in... | |||
T17232 | Vidupiprant | AMG 853 | Prostaglandin Receptor |
Vidupiprant (AMG 853) is an effective dual antagonist of CRTH2 and prostanoid D receptor with IC50s of 8 nM and 35 nM in human plasma. Vidupiprant can be used in studies about the treatment of asthma. | |||
T4635 | Ralinepag | APD811 | Others , Prostaglandin Receptor |
Ralinepag (APD811) is a potent, orally bioavailable agonist of non-prostanoid prostacyclin (IP) receptor, with EC50s of 8.5 nM, 530 nM and 850 nM for human and rat IP receptor and human DP1 receptor, respectively. | |||
T2528 | Latanoprost | Xalatan,PHXA41 | GPR , Prostaglandin Receptor , RAR/RXR |
Latanoprost (Xalatan) is a prostaglandin F2alpha analogue and a prostanoid selective FP receptor agonist with an ocular hypertensive effect. | |||
T1978 | GW627368 | GW 627368X | Prostaglandin Receptor |
GW627368 (GW 627368X)X is a novel, potent and selective antagonist of prostanoid EP4 receptor. | |||
T11211 | EP4 receptor antagonist 1 | Prostaglandin Receptor | |
EP4 Receptor Antagonist 1 is a highly potent and selective competitive prostanoid EP4 receptor antagonist, effective for cancer immunotherapy. It inhibits both human and mouse EP4 receptors with IC50 values of 6.1 nM and... | |||
T2664 | Timapiprant | OC000459 | GPR , Prostaglandin Receptor |
Timapiprant (OC000459) is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM). | |||
T15718 | Latanoprost acid | GPR | |
Latanoprost acid is a selective agonist of prostanoid receptors and inhibits RANKL-induced osteoclastogenesis and function through the inhibition of c-fos/NFATc1 pathway. Latanoprost acid can be used in studies about low... | |||
T69602 | ONO-DI-004 | ||
ONO-DI-004 is a selective EP1 Prostanoid receptor agonist. | |||
T26578 | AH13205 | AH-13205,AH 13205 | |
AH13205 is an agonist of EP2 prostanoid receptor. | |||
T29813 | AL-3138 | AL3138,AL 3138,11-Deoxy-16-fluoro PGF2alpha | |
AL-3138 is a prostaglandin F2alpha (PGF2alpha) analogue which antagonizes FP prostanoid receptor-mediated inositol phosphates generation. | |||
T27765 | L-644,698 | ||
L-644,698 is a selective agonist of human prostanoid DP receptor. | |||
T20644 | Unoprostone isopropyl | UF021,Rescula,UF-021,UF 021 | |
Unoprostone isopropyl, a prostanoid and synthetic docosanoid, is approved for the treatment of ocular hypertension and open-angle glaucoma. | |||
T19660 | QCC-374 | QCC374 | |
QCC-374 is a prostanoid agonist. It potentially for the treatment of pulmonary arterial hypertension. | |||
T27875 | LY 150310 | LY150310,LY-150310 | |
LY 150310, a histamine H1-receptor antagonist, can alter prostanoid concentrations in vitro and in vivo. | |||
T28651 | S-5751 | S 5751 | |
S-5751, a prostanoid DP (DP1) antagonist, is used potentially for the treatment of bronchial asthma. | |||
T29734 | AH 19437 | AH-19437,AH19437 | |
AH 19437 is a prostanoid receptor. | |||
T15690 | L-902688 | Prostaglandin Receptor | |
L-902688 is an orally active EP4 receptor agonist (Ki: 0.38 nM; EC50: 0.6 nM). L-902688 displays >4,000-fold selective for EP4 over other EP and prostanoid receptors. | |||
T28032 | MF266-1 | MF 266-1,MF-266-1 | |
MF266-1, a selective E prostanoid receptor 4 antagonist, relieves joint inflammation and pain in rodent models of osteoarthritis and rheumatoid. | |||
T16389 | Omidenepag | Prostaglandin Receptor | |
Omidenepag is a pharmacologically active form of Omidenepag Isopropyl and is a selective, non-prostanoid EP2 receptor agonist (EC50: 1.1 nM). Omidenepag displays binding affinities (IC50: 10 nM for h-EP2). |