| T63667 |
ONO-8713
|
459411-08-6
|
100%
|
|
|
ONO-8713 is a selective prostaglandin E receptor subtype EP1 antagonist that can be used to study diseases of the biblical system and metabolism-related diseases...
|
| T2428 |
TG6-10-1
|
1415716-58-3
|
100%
|
|
|
TG6-10-1 is an EP2 antagonist.
|
| TN1257 |
3-O-Acetyl-α-boswellic acid
|
89913-60-0
|
100%
|
|
|
3-O-Acetyl-α-boswellic acid (α-Boswellic acid acetate) has strong anti-inflammatory activity.
|
| T77699 |
EP4-IN-1
|
2455480-28-9
|
100%
|
|
|
EP4-IN-1 is a potent prostaglandin EP4 receptor inhibitor with potential anti-tumor, anti-inflammatory and analgesic activities for the study of immune and tumor...
|
| T13563 |
AZ-1355
|
75451-07-9
|
100%
|
|
|
AZ-1355 is a novel dibenzoxepine derivative with lipid-lowering properties.
|
| T0795 |
Rutin
|
153-18-4
|
95%
|
|
|
Rutin (Quercetin 3-O-rutinoside), a flavonoid, has a variety of biological activities including antiallergic, anti-inflammatory, antiproliferative, and anticarci...
|
| T16280 |
Nedocromil
|
69049-73-6
|
95%
|
|
|
Nedocromil (FPL 59002) inhibits the action or formation of multiple mediators. Which including histamine, leukotriene C4 (LTC4), and prostaglandin D2 (PGD2).
|
| T27084 |
Crisdesalazine
|
927685-43-6
|
95.95%
|
|
|
Crisdesalazine (AAD 2004) is an inhibitor of microsomal prostaglandin E2 synthase-1 (mPGES-1). Crisdesalazine reduces autophagosome formation, axonopathy, and mo...
|
| T10960L |
Darbufelone mesylate
|
139340-56-0
|
96.81%
|
|
|
Darbufelone mesylate (CI-1004 mesylate) inhibited PGF2α and LTB4 in cells. Darbufelone mesylate inhibited PGHS-2 with IC50 value of 0.19 μM and PGHS-1 with IC50 ...
|
| T27630 |
Isbogrel
|
89667-40-3
|
97.06%
|
|
|
Isbogrel (CV4151) is a small molecule thromboxane A2 synthase (TXA2 synthase) inhibitor that can be used to study cardiac arrhythmias, transient ischemic attacks...
|
| T6485 |
Embelin
|
550-24-3
|
97.07%
|
|
|
Embelin (Embelic acid), isolated from the Japanese Ardisia herb, is an inhibitor of the X-linked inhibitor of apoptosis (IC50: 4.1 uM).
|
| T14148 |
AH 6809
|
33458-93-4
|
97.59%
|
|
|
AH 6809 is an antagonist of EP and DP receptor(with Kis of 1217, 1150, 1597, and 1415 nM for the cloned human EP1, EP2, EP3-III, and DP receptor respectively). A...
|
| T21738 |
PF-9184
|
1221971-47-6
|
97.64%
|
|
|
PF-9184 is a potent and selective inhibitor of human microsomal prostaglandin E synthase-1 (mPGES-1), IC50 =16.5 nM. PF-9184 inhibits IL-1β-induced PGE2 synthesi...
|
| T21976 |
ONO-8130
|
459841-96-4
|
97.82%
|
|
|
ONO-8130 is an orally available antagonist of EP1 receptor.
|
| T28089 |
MPGES-1 Inhibitor-1
|
1381846-21-4
|
97.90%
|
|
|
mPGES-1 Inhibitor-1 is a novel selective inhibitor of microsomal prostaglandin E synthase-1 (mPGES-1) with anti-inflammatory and analgesic activity for the study...
|
| T0159 |
Pranoprofen
|
52549-17-4
|
97.99%
|
|
|
Pranoprofen (Pyranoprofen) (INN) is a non-steroidal anti-inflammatory drug used in ophthalmology.
|
| T3965 |
Fevipiprant
|
872365-14-5
|
98%
|
|
|
Fevipiprant (NVP-QAW039) is a selective, potent, reversible competitive CRTh2 antagonist.
|
| T5758 |
Sphondin
|
483-66-9
|
98%
|
|
|
Sphondin has anticonvulsant, anti-inflammatory, and anti-proliferative activities, it possessed an inhibitory effect on IL-1beta-induced increase in the level of...
|
| T5847 |
Cloprostenol sodium salt
|
55028-72-3
|
98%
|
|
|
Cloprostenol sodium salt (ICI 80996 sodium salt) is a more water solute, crystalline form of cloprostenol than the free acid, is a synthetic analog of prostaglan...
|
| TN1650 |
Friedelin
|
559-74-0
|
98%
|
|
|
Friedelin possesses antioxidant, gastroprotective, anti-diarrhoeal, liver protective, anti-inflammatory, analgesic and antipyretic activities.
|
