Flumetasone
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(Redirected from Flumethasone)
| Systematic (IUPAC) name | |
|---|---|
| (1R,2S,8S,10S,11S,13R,14R,15S,17S)-1,8-difluoro-14,17-dihydroxy-14-(2-hydroxyacetyl)-2,13,15-trimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-3,6-dien-5-one | |
| Clinical data | |
| AHFS/Drugs.com | Micromedex Detailed Consumer Information |
| Topical | |
| Pharmacokinetic data | |
| Metabolism | Hepatic, CYP3A4-mediated |
| Identifiers | |
| 2135-17-3 |
|
| D07AB03 , D07XB01 (combinations), QH02AB90 | |
| PubChem | CID 16490 |
| UNII | LR3CD8SX89 |
| KEGG | D04208 |
| ChEMBL | CHEMBL1201392 |
| Synonyms | (6S,8S,9S,10S,11S,13S,14S,16R,17R)-6,9-difluoro-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13,16-trimethyl-6,7,8,11,12,14,15,16-octahydrocyclopenta[a]phenanthren-3-one |
| Chemical data | |
| Formula | C22H28F2O5 |
| 410.452 g/mol | |
| |
Flumethasone (usually as the pivalic acid ester flumethasone pivalate, trade name Locacorten or Locorten) is a corticosteroid for topical use. It is available in combination with clioquinol, under the trade name Locacorten-Vioform (in some countries Locorten-Vioform), for the treatment of otitis externa and otomycosis.
Flumethasone shows fully 420 times the potency of cortisone in an animal model for anti-inflammatory activity.
Synthesis[edit]
Flumethasone synthesis:[1]
See also[edit]
References[edit]
- ^ Edwards, J. A.; Ringold, H. J.; Djerassi, C. (1959). "STEROIDS. CXXII.16α-FLUORO-16α-METHYLCORTI-COIDS—SYNTHESIS AND BIOLOGICAL ACTIVITY". Journal of the American Chemical Society 81 (12): 3156. doi:10.1021/ja01521a073.
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