Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C22H27FO5 |
Molecular Weight | 390.4452 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC(=C)[C@](O)(C(=O)CO)[C@@]1(C)C[C@H](O)[C@@]3(F)[C@@]2([H])CCC4=CC(=O)C=C[C@]34C
InChI
InChIKey=YVHXHNGGPURVOS-SBTDHBFYSA-N
InChI=1S/C22H27FO5/c1-12-8-16-15-5-4-13-9-14(25)6-7-19(13,2)21(15,23)17(26)10-20(16,3)22(12,28)18(27)11-24/h6-7,9,15-17,24,26,28H,1,4-5,8,10-11H2,2-3H3/t15-,16-,17-,19-,20-,21-,22-/m0/s1
Molecular Formula | C22H27FO5 |
Molecular Weight | 390.4452 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 7 / 7 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
DescriptionSources: http://www.pharmazie.com/graphic/A/49/0-14349.pdf
Sources: http://www.pharmazie.com/graphic/A/49/0-14349.pdf
Fluprednidene (used in a form of fluprednidene 21-acetate) is a glucocorticoid developed for the treatment of inflammatory skin diseases. The drug is marketed under the name Decoderm in Europe.
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Steroid-induced dermal atrophy. Investigations on discontinuous application. | 1989 |
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[Optimized interval treatment of eczema with fluprednidene. A multicenter double-blind study]. | 1989 Sep 15 |
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Dermal absorption of fluprednidene-21-acetate and miconazole from a new topical preparation in pigs. | 1994 Nov |
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Double-blind comparison of miconazole/corticosteroid combination versus miconazole in inflammatory dermatomycoses. | 1995 Feb |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://www.pharmazie.com/graphic/A/49/0-14349.pdf
Apply the cream to the affected skin areas once a day.
Route of Administration:
Topical
Substance Class |
Chemical
Created
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Record UNII |
FA517NS3N7
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Record Status |
Validated (UNII)
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QD07CB02
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C521
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D07AB07
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QD07AB07
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CHEMBL2106763
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Related Record | Type | Details | ||
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ACTIVE MOIETY |