| Weight | 524.626 g/mol |
|---|---|
| Formula | C30H28CaO6 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 8 |
Fenoprofen calcium (34597-40-5)
Fenoprofen · Nalfon · Fenoprofen, Anhydrous, Calcium Salt
Score:
#1396 in Biochemistry
,
#3345 in Biology
,
#4169 in Chemistry
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- Capillary electrophoretic chiral separations with cyclodextrin additives: I. acids: Chiral selectivity as a function of pH and the concentration of -cyclodextrin for fenoprofen and ibuprofen (Journal of Chromatography A, 1993)
- Fenoprofen nephropathy: lipoid nephrosis and interstitial nephritis. A possible T-lymphocyte disorder. (The American Journal of Medicine, 1982)
- Stereoselective Inversion of (R)-Fenoprofen to (S)-Fenoprofen in Humans (Journal of Pharmaceutical Sciences, 1985)
- Crystal structure of an inclusion complex of .beta.-cyclodextrin with racemic fenoprofen: direct evidence for chiral recognition (Journal of the American Chemical Society, 1988)
- Gastrointestinal Blood Loss: Effect of Aspirin, Fenoprofen, and Acetaminophen in Rheumatoid Arthritis as Determined by Sequential Gastroscopy and Radioactive Fecal Markers (JAMA, 1977)
- The stereospecific incorporation of fenoprofen into rat hepatocyte and adipocyte triacylglycerols (Biochemical Pharmacology, 1988)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Fenoprofen
- Nalfon
- Fenoprofen, Anhydrous, Calcium Salt
- Fenoprofen Dihydrate, Calcium Salt
- Nalgesic
-
SMILESCC(C1=CC(=CC=C1)OC2=CC=CC=C2)C(=O)O.CC(C1=CC(=CC=C1)OC2=CC=CC=C2)C(=O)O.[Ca]
-
InChIKeyNRZVLXYXXJDVKN-UHFFFAOYSA-N
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Synthesis
Reactant
+
phenoxyalcohol
(Dakin oxidation)
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