Name | potassium,3-(4,5-diphenyl-1,3-oxazol-2-yl)propanoate |
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Synonyms |
oxaprozin potassium salt
potassium 3-(4,5-diphenyl-1,3-oxazol-2-yl)propanoate Daypro Alta ML56O2Z92I UNII-ML56O2Z92I 2-Oxazolepropanoic acid,4,5-diphenyl-,potassium salt OXAPROZIN POTASSIUM 4,5-diphenyl-2-oxazolepropionic acid potassium salt |
Description | Oxaprozin potassium is an orally active and potent COX inhibitor, with IC50 values of 2.2 μM for human platelet COX-1 and and 36 μM for IL-1-stimulated human synovial cell COX-2, respectively. Oxaprozin potassium also inhibits the activation of NF-κB. Oxaprozin potassium induces cell apoptosis. Oxaprozin potassium shows anti-inflammatory activity. Oxaprozin potassium-mediated inhibition of the Akt/IKK/NF-κB pathway contributes to its anti-inflammatory properties[1][2]. |
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Related Catalog | |
Target |
COX-1:2.2 μM (IC50) COX-2:36 μM (IC50) NF-κB Akt pAKT IKK |
In Vitro | Oxaprozin (0-100 μM) induces apoptosis in a dose-dependent manner. Oxaprozin increases caspase-3 activity in the activated but not in the resting condition. NF-κB activation is inhibited by Oxaprozin (50 μM). Oxaprozin inhibits activation of the IKK system induced by the reagent IκBα[1]. Oxaprozin (100 μM) induces the strongest proapoptotic effect and significantly increases CD40L-treated monocyte apoptosis. Oxaprozin treatment inhibits CD40L-induced Akt and NF-κB (p65) phosphorylation[2]. |
References |
Boiling Point | 467ºC at 760mmHg |
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Molecular Formula | C18H14KNO3 |
Molecular Weight | 331.40700 |
Flash Point | 236.2ºC |
Exact Mass | 331.06100 |
PSA | 66.16000 |
LogP | 2.69110 |
Vapour Pressure | 1.6E-09mmHg at 25°C |