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Search Results for " prostanoid "

20

Compounds

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).
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