Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C16H12O4 |
| Molecular Weight | 268.2641 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)CC1=CC=C2C(OCC3=CC=CC=C3C2=O)=C1
InChI
InChIKey=PYIHCGFQQSKYBO-UHFFFAOYSA-N
InChI=1S/C16H12O4/c17-15(18)8-10-5-6-13-14(7-10)20-9-11-3-1-2-4-12(11)16(13)19/h1-7H,8-9H2,(H,17,18)
Oxepinac was developed as an anti-inflammatory drug. Results of clinical trials have revealed that oxepinac was an effective and well-tolerated drug in the treatment of painful osteoarthritis. Experiments on animal have shown that oxepinac had no teratogenic effect on fetuses in mice and rabbits. Information about the current use of this drug is not available.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Quantitative analysis of oxepinac in human plasma, urine and saliva by gas chromatography--mass fragmentography. | 1980-04-11 |
|
| Nonsteroidal antiinflammatory agents. 2. Derivatives/analogues of dibenz[b,e]oxepin-3-acetic acid. | 1978-07 |
|
| Teratogenicity study of oxepinac in mice and rabbits. | 1978 |
|
| Acute, subacute and chronic toxicity of oxepinac. | 1978 |
|
| Multi-centered clinical evaluation of oxepinac against peripheral arthropathy particularly osteoarthritis. | 1978 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/350232
Male 31, female 104, and the age distribution are 37--82 years and 62 years in average. Three groups of the doses, 75 mg, 150 mg, 300 mg daily, respectively, were administered for two weeks.
Route of Administration:
Oral
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NCI_THESAURUS |
C257
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ACTIVE MOIETY