Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C16H12FNO3 |
Molecular Weight | 285.2698 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 1 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C[C@H](C(O)=O)C1=CC2=C(OC(=N2)C3=CC=C(F)C=C3)C=C1
InChI
InChIKey=ARPYQKTVRGFPIS-VIFPVBQESA-N
InChI=1S/C16H12FNO3/c1-9(16(19)20)11-4-7-14-13(8-11)18-15(21-14)10-2-5-12(17)6-3-10/h2-9H,1H3,(H,19,20)/t9-/m0/s1
Flunoxaprofen is a chiral nonsteroidal anti-inflammatory drug (NSAID). It is an arylalkanoic acid derivative. Flunoxaprofen inhibits leukotriene rather than prostaglandin synthesis. Its potency was comparable with that of indomethacin and higher than that of acetyl salicylic acid, ibuprofen or phenylbutazone. The analgesic activity of flunoxaprofen, evaluated by the hot plate method and tail pinching in mice, was slightly lower than that of indomethacin but higher than that of acetyl salicylic acid and ibuprofen. Its adverse reactions profile is similar to the profiles of other NSAIDs, including gastrointestinal disturbances. Flunoxaprofen was withdrawn from clinical use because of concerns of potential hepatotoxicity.
Approval Year
PubMed
Title | Date | PubMed |
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Interference of the new antiinflammatory compound flunoxaprofen with eicosanoid formation in various biological systems. | 1987 Jan |
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Determination of the non-steroidal anti-inflammatory drug flunoxaprofen, S(+)-2-(4-fluorophenyl)-alpha-methyl-5-benzoxazoleacetic acid, in blood and urine by high-performance liquid chromatography. | 1987 Jan 23 |
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Flunoxaprofen, a new non-steroidal anti-inflammatory drug, does not interfere with prostaglandin synthesis in rat gastric mucosa. | 1989 Mar-Apr |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3670687
100 mg twice a day for a 60 days period
Route of Administration:
Oral
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QM01AE15
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M01AE15
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NCI_THESAURUS |
C257
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G02CC04
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SUB07713MIG
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DB13317
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76154
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FLUNOXAPROFEN
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C045356
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m5449
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4870
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ACTIVE MOIETY