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174064-08-5

174064-08-5 structure
174064-08-5 structure
  • Name: Oxaprozin, potassium salt
  • Chemical Name: potassium,3-(4,5-diphenyl-1,3-oxazol-2-yl)propanoate
  • CAS Number: 174064-08-5
  • Molecular Formula: C18H14KNO3
  • Molecular Weight: 331.40700
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2016-06-12 15:36:17
  • Modify Date: 2024-01-22 06:40:05
  • 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].

Name potassium,3-(4,5-diphenyl-1,3-oxazol-2-yl)propanoate
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].
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

[1]. Ottonello L, et al. Delayed apoptosis of human monocytes exposed to immune complexes is reversed byoxaprozin: role of the Akt/IkappaB kinase/nuclear factor kappaB pathway. Br J Pharmacol. 2009 May;157(2):294-306.

[2]. Montecucco F, et al. Oxaprozin-induced apoptosis on CD40 ligand-treated human primary monocytes is associated with the modulation of defined intracellular pathways. J Biomed Biotechnol. 2009;2009:478785.

Boiling Point 467ºC at 760mmHg
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