T15259 |
Evatanepag
|
223488-57-1
|
99.68%
|
|
Evatanepag (CP-533536 free acid) is an EP2 receptor selective prostaglandin E2 (PGE2) agonist that induces local bone formation with EC50 of 0.3 nM.CP-533536 dem...
|
T10098 |
PGS-IN-1
|
102271-49-8
|
99.67%
|
|
PGS-IN-1 (KME-4) is a potent inhibitor of prostaglandin synthetase (PGS, IC50: 0.28 μM) and 5-lipoxygenase (IC50: 1.05 μM).
|
T17039 |
Terbogrel
|
149979-74-8
|
99.65%
|
|
Terbogrel is an oral thromboxane A2 receptor antagonist (IC50 is about 10 nM) and thromboxane A2 synthase inhibitor (IC50 is about 10 nM). Terbogrel is an antipl...
|
T14865 |
Carboprost tromethamine
|
58551-69-2
|
99.61%
|
|
Carboprost tromethamine, a synthetic 15-methyl analogue of prostaglandin F2α, effectively promotes uterine contractions and significantly reduces bleeding during...
|
T67946 |
EP2 receptor antagonist-2
|
615273-95-5
|
99.59%
|
|
EP2 receptor antagonist-2 (CID891729) is a compound that not only serves as an antagonist to the EP2 receptor, blocking its activation by PGE2, but also reduces ...
|
TN1440 |
Beta-Hydroxyisovalerylshikonin
|
7415-78-3
|
99.59%
|
|
Beta-Hydroxyisovalerylshikonin is an inhibitor of protein-tyrosine kinases such as v-Src and EGFR, and has been shown to induce apoptosis in several human tumor ...
|
T3S2007 |
MRE-269
|
475085-57-5
|
99.57%
|
|
MRE-269 (ACT-333679) is an orally available and long-acting prostacyclin receptor agonist prodrug. MRE-269(ACT-333679) is used for the treatment of pulmonary art...
|
TMA0536 |
2-Acetylbenzoic acid
|
577-56-0
|
99.57%
|
|
2-Acetylbenzoic acid is more potent than 2-propionyloxybenzoic acid in inhibiting platelet function and platelet prostaglandin (PG) synthesis although the potenc...
|
T2690 |
Tranilast
|
53902-12-8
|
99.57%
|
|
Tranilast (SB 252218), an antiallergic drug, suppresses lipid mediator and cytokine release from inflammatory cells, therefore utilized in the treatment of aller...
|
T21224 |
(+)-Fluprostenol
|
54276-17-4
|
99.56%
|
|
(+)-Fluprostenol (AL-5848), an analogue of prostaglandin F2 alpha, is a prostaglandin F2α receptor PTGFR agonist and decreases the expression of Oviductal glycop...
|
T62061 |
COX-2-IN-6
|
2756347-91-6
|
99.56%
|
|
COX-2-IN-6 is a potent, selective, and orally available cyclooxygenase-2 (COX-2) inhibitor with an IC50 of 0.84 μM and a Ki of 69 nM.COX-2-IN-6 inhibits COX-2-dr...
|
T7053 |
P-Hydroxycinnamic acid
|
7400-08-0
|
99.55%
|
|
p-Hydroxycinnamic acid (NSC-59260) can inhibit platelet activity, with IC50s of 371 μM, 126 μM for thromboxane B2 production and lipopolysaccharide-induced prost...
|
T0212 |
Seratrodast
|
112665-43-7
|
99.54%
|
|
Seratrodast (ABT-001) (INN), a thromboxane A2 (TXA2) receptor (TP receptor) antagonist, is mainly used in the therapy of asthma. It was the first TP receptor ant...
|
T6399 |
AZD1981
|
802904-66-1
|
99.54%
|
|
AZD1981 is an effective and specific CRTh2 (DP2) receptor antagonist (IC50: 4 nM), showing >1000-fold selectivity over more than 340 other enzymes and receptors,...
|
T1978 |
GW627368
|
439288-66-1
|
99.54%
|
|
GW627368 (GW 627368X)X is a novel, potent and selective antagonist of prostanoid EP4 receptor.
|
T11211 |
EP4 receptor antagonist 1
|
2287259-07-6
|
99.53%
|
|
EP4 Receptor Antagonist 1 is a highly potent and selective competitive prostanoid EP4 receptor antagonist, effective for cancer immunotherapy. It inhibits both h...
|
T68155 |
Tebufelone
|
112018-00-5
|
99.52%
|
|
Tebufelone is a potent in vitro inhibitor of CO , a novel non-steroidal anti-inflammatory drug (NSAID) belonging to the di-tert-butylphenol (DTBP) class that has...
|
TQ0292 |
Grapiprant
|
415903-37-6
|
99.49%
|
|
Grapiprant (AAT-007) is a selective EP4 receptor antagonist. Grapiprant displaces [3H]-PGE2 (1 nM) binding to dog recombinant EP4 receptor (IC50: 35 nM, Ki: 24 n...
|
T24567 |
Octimibate
|
89838-96-0
|
99.49%
|
|
Octimibate (Octimibato) is a non-prostaglandin platelet aggregation inhibitor and cyclic prostaglandin agonist.Octimibate is used in the treatment of cardiovascu...
|
T2791 |
Pectolinarin
|
28978-02-1
|
99.47%
|
|
Pectolinarin is a Cirsium isolate with anti-inflammatory activity.
|