Phenopyrazone
Phenopyrazone (Diphenox), a derivative of Antipyrine (HY-B0171), exhibits oral activity as well as analgesic, antipyretic, anti-inflammatory, and antidiarrheal properties. Phenopyrazone can be used in research related to headache, rheumatism, chronic diarrhea and varicose veins.
For research use only. We do not sell to patients.
- CAS No.: 3426-01-5
- Formula: C15H12N2O2
- Molecular Weight:252.27
-
Storage:
Please store the product under the recommended conditions in the Certificate of Analysis.
Biological Activity
Description
In Vivo
Phenopyrazone (p.o.; single dose) alone has no detectable antipyretic activity against yeast-induced fever in rats at oral doses up to 640 mg/kg[1].
Phenopyrazone (p.o.) exhibits anti-inflammatory activity against carrageenin-induced hind paw edema in rats with an ED50 of 574.0 mg/kg p.o[1].
Phenopyrazone (oral administration) serves as a component in preparations for venous disorders and induces pseudo‑lupus syndrome accompanied by high‑titer antimitochondrial antibodies[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
-
CAS No. 3426-01-5
-
Molecular Weight 252.27
-
Formula C15H12N2O2
-
SMILES
O=C1NN(C=2C=CC=CC2)C(=O)C1C=3C=CC=CC3
-
Synonyms
Diphenox; Kr 132
-
Shipping
Room temperature in continental US; may vary elsewhere.
-
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Protocols
-
Research Protocol for Inflammation-related Diseases
The NLRP3 inflammasome is a cytosolic innate immune signaling platform that integrates priming signals and danger-signal activation to promote caspase-1 activation, maturation of IL-1β and IL-18, and gasdermin D-mediated pyroptotic cell death. The core experimental logic is to determine whether inflammatory disease phenotypes are driven by increased NLRP3 expression, ASC-containing inflammasome assembly, caspase-1 cleavage, GSDMD cleavage, and extracellular release of IL-1β/IL-18 rather than by nonspecific cell injury alone. The pathway is strongly linked to inflammation-related disease phenotypes because monosodium urate crystals activate NALP3/NLRP3 inflammasome signaling in gout-like crystal inflammation, cholesterol crystals activate NLRP3 inflammasomes in atherogenesis models, and DSS-induced intestinal inflammation has been reported to involve NLRP3 inflammasome activity. However, experimental colitis studies also show context-dependent protective effects of NLRP3 inflammasome co
Purity & Documentation
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)