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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H29FO5
Molecular Weight 392.4611
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUPEROLONE

SMILES

[H][C@@]12CC[C@](O)(C(=O)[C@H](C)O)[C@@]1(C)C[C@H](O)[C@@]3(F)[C@@]2([H])CCC4=CC(=O)C=C[C@]34C

InChI

InChIKey=SLVCCRYLKTYUQP-DVTGEIKXSA-N
InChI=1S/C22H29FO5/c1-12(24)18(27)21(28)9-7-15-16-5-4-13-10-14(25)6-8-19(13,2)22(16,23)17(26)11-20(15,21)3/h6,8,10,12,15-17,24,26,28H,4-5,7,9,11H2,1-3H3/t12-,15-,16-,17-,19-,20-,21-,22-/m0/s1

HIDE SMILES / InChI

Molecular Formula C22H29FO5
Molecular Weight 392.4611
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Fluperolone (P-1742 or Methral) is a topical fluorinated prednisolone derivative exerting an anti-inflammatory activity. It demonstrated effectivity in the treatment of various dermatoses.

Approval Year

PubMed

PubMed

TitleDatePubMed
A clinical trial of Fluperolone, a new topical steroid.
1963 Mar
A NEW SYNTHETIC CORTICOSTEROID--P.1742.
1964 Aug
CLINICAL TRIAL OF P-1742 TOPICAL OR FLUPEROLONE (9 FLUORO-21 METHYL PREDNISOLONE) IN PSORIASIS.
1964 Jun

Sample Use Guides

0.1% ointment
Route of Administration: Transdermal
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:44:39 UTC 2023
Edited
by admin
on Fri Dec 15 18:44:39 UTC 2023
Record UNII
S33056JLS5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUPEROLONE
INN   WHO-DD  
INN  
Official Name English
Fluperolone [WHO-DD]
Common Name English
9-FLUORO-11.BETA.,17.ALPHA.-DIHYDROXY-17-(S)-LACTOYLANDROSTA-1,4-DIEN-3-ONE
Common Name English
fluperolone [INN]
Common Name English
ANDROSTA-1,4-DIEN-3-ONE, 9-FLUORO-11,17-DIHYDROXY-17-(2-HYDROXY-1-OXOPROPYL)-, (11.BETA.,17.ALPHA.)-
Common Name English
ANDROSTA-1,4-DIEN-3-ONE, 9-FLUORO-11.BETA.,17.ALPHA.-DIHYDROXY-17-LACTOYL-
Common Name English
Classification Tree Code System Code
WHO-VATC QD07AB05
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
WHO-ATC D07AB05
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
Code System Code Type Description
FDA UNII
S33056JLS5
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
INN
1473
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
SMS_ID
100000080719
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
NCI_THESAURUS
C169994
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
CAS
3841-11-0
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
DRUG CENTRAL
3237
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
EPA CompTox
DTXSID60191746
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
WIKIPEDIA
Fluperolone
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
PUBCHEM
56841872
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
DRUG BANK
DB13491
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
ChEMBL
CHEMBL2107401
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
EVMPD
SUB07729MIG
Created by admin on Fri Dec 15 18:44:39 UTC 2023 , Edited by admin on Fri Dec 15 18:44:39 UTC 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY