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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H29FO6
Molecular Weight 432.4819
Optical Activity UNSPECIFIED
Defined Stereocenters 7 / 7
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUPREDNIDENE ACETATE

SMILES

CC(=O)OCC(=O)[C@@]1(O)C(=C)C[C@H]2[C@@H]3CCC4=CC(=O)C=C[C@]4(C)[C@@]3(F)[C@@H](O)C[C@]12C

InChI

InChIKey=DEFOZIFYUBUHHU-IYQKUMFPSA-N
InChI=1S/C24H29FO6/c1-13-9-18-17-6-5-15-10-16(27)7-8-21(15,3)23(17,25)19(28)11-22(18,4)24(13,30)20(29)12-31-14(2)26/h7-8,10,17-19,28,30H,1,5-6,9,11-12H2,2-4H3/t17-,18-,19-,21-,22-,23-,24-/m0/s1

HIDE SMILES / InChI

Molecular Formula C24H29FO6
Molecular Weight 432.4819
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 7 / 7
E/Z Centers 0
Optical Activity UNSPECIFIED

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

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
DECODERM

Approved Use

For the treatment of inflammatory skin diseases, for example, atopic eczema (atopic dermatitis, endogenous eczema), contact dermatitis.
Doses

Doses

DosePopulationAdverse events​
0.1 % single, topical
Recommended
Dose: 0.1 %
Route: topical
Route: single
Dose: 0.1 %
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
Disc. AE: Hypersensitivity...
AEs leading to
discontinuation/dose reduction:
Hypersensitivity
Sources:
AEs

AEs

AESignificanceDosePopulation
Hypersensitivity Disc. AE
0.1 % single, topical
Recommended
Dose: 0.1 %
Route: topical
Route: single
Dose: 0.1 %
Sources:
unhealthy, ADULT
Health Status: unhealthy
Age Group: ADULT
Sex: M+F
Food Status: UNKNOWN
Sources:
PubMed

PubMed

TitleDatePubMed
Double-blind comparison of miconazole/corticosteroid combination versus miconazole in inflammatory dermatomycoses.
1995-02
Dermal absorption of fluprednidene-21-acetate and miconazole from a new topical preparation in pigs.
1994-11
[Optimized interval treatment of eczema with fluprednidene. A multicenter double-blind study].
1989-09-15
Steroid-induced dermal atrophy. Investigations on discontinuous application.
1989
Patents

Sample Use Guides

Apply the cream to the affected skin areas once a day.
Route of Administration: Topical
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:47:02 GMT 2025
Edited
by admin
on Mon Mar 31 17:47:02 GMT 2025
Record UNII
GE65DV564S
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUPREDNIDENE ACETATE
MART.   MI   WHO-DD  
Common Name English
FLUPREDNIDENE ACETATE [MI]
Preferred Name English
FLUPREDNIDENE ACETATE [MART.]
Common Name English
Fluprednidene acetate [WHO-DD]
Common Name English
Code System Code Type Description
MESH
C100064
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
DRUG CENTRAL
3238
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
CAS
1255-35-2
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
SMS_ID
100000091890
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
PUBCHEM
9980241
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
MERCK INDEX
m5492
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY Merck Index
DRUG BANK
DB08970
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
FDA UNII
GE65DV564S
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
RXCUI
25194
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY RxNorm
WIKIPEDIA
FLUPREDNIDENE ACETATE
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
EVMPD
SUB02235MIG
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
EPA CompTox
DTXSID0048719
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
ECHA (EC/EINECS)
215-013-9
Created by admin on Mon Mar 31 17:47:02 GMT 2025 , Edited by admin on Mon Mar 31 17:47:02 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY