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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H25Cl2FO5
Molecular Weight 447.325
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUCLOROLONE

SMILES

[H][C@@]12C[C@@H](O)[C@](O)(C(=O)CO)[C@@]1(C)C[C@H](Cl)[C@@]3(Cl)[C@@]2([H])C[C@H](F)C4=CC(=O)C=C[C@]34C

InChI

InChIKey=VTWKPILBIUBMDS-OTJLYDAYSA-N
InChI=1S/C21H25Cl2FO5/c1-18-4-3-10(26)5-13(18)14(24)6-12-11-7-16(27)21(29,17(28)9-25)19(11,2)8-15(22)20(12,18)23/h3-5,11-12,14-16,25,27,29H,6-9H2,1-2H3/t11-,12-,14-,15-,16+,18-,19-,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula C21H25Cl2FO5
Molecular Weight 447.325
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 9 / 9
E/Z Centers 0
Optical Activity UNSPECIFIED

Fluclorolone is a synthetic glucocorticoid corticosteroid which was never marketed. The acetonide cyclic ketal of fluclorolone, fluclorolone acetonide is a corticosteroid for topical use on the skin. Fluclorolone is a glucocorticoid receptor agonist. It was used for the treatment of atopic dermatitis, varicose eczema and psoriasis.

Approval Year

PubMed

PubMed

TitleDatePubMed
Clinical trial of fluclorolone acetonide in FAPG base in the treatment of varicose eczema.
1974

Sample Use Guides

A double-blind trial comparing fluclorolone acetonide 0.025 % in FAPG base with the base alone was carried out on 18 female patients with varicose eczema. In 2 patients both legs were affected and treated. All the patients were routinely treated by compression sclerotherapy and the areas of eczema dressed once weekly with one or other of the creams until the eczema had cleared or there had been 4 visits with little or no improvement. Eight out of 10 patients treated with the active cream healed after one application and 1 patient after a second application, compared with only 1 patient healed and 1 showing some improvement on the base alone.
Route of Administration: Topical
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:14:46 UTC 2023
Edited
by admin
on Fri Dec 15 15:14:46 UTC 2023
Record UNII
036B9W83KK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUCLOROLONE
Common Name English
PREGNA-1,4-DIENE-3,20-DIONE, 9,11.BETA.-DICHLORO-6.ALPHA.-FLUORO-16.ALPHA.,17,21-TRIHYDROXY-
Systematic Name English
PREGNA-1,4-DIENE-3,20-DIONE, 9,11-DICHLORO-6-FLUORO-16,17,21-TRIHYDROXY-, (6.ALPHA.,11.BETA.,16.ALPHA.)-
Systematic Name English
Classification Tree Code System Code
WHO-ATC D07AC02
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
WHO-VATC QD07AC02
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
Code System Code Type Description
DRUG BANK
DB13856
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
ChEMBL
CHEMBL3707231
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
PUBCHEM
76962649
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
FDA UNII
036B9W83KK
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
WIKIPEDIA
Fluclorolone
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
DRUG CENTRAL
4546
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
EPA CompTox
DTXSID601317985
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
CAS
3693-38-7
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY
RXCUI
108091
Created by admin on Fri Dec 15 15:14:46 UTC 2023 , Edited by admin on Fri Dec 15 15:14:46 UTC 2023
PRIMARY RxNorm
Related Record Type Details
ACTIVE MOIETY