FLUOCINOLONE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Investigational

Investigational

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C21H26F2O6
Molecular Weight	412.4243
Optical Activity	UNSPECIFIED
Defined Stereocenters	9 / 9
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of FLUOCINOLONE

Structure Search

SMILES

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

InChI

InChIKey=UUOUOERPONYGOS-CLCRDYEYSA-N

InChI=1S/C21H26F2O6/c1-18-4-3-10(25)5-13(18)14(22)6-12-11-7-15(26)21(29,17(28)9-24)19(11,2)8-16(27)20(12,18)23/h3-5,11-12,14-16,24,26-27,29H,6-9H2,1-2H3/t11-,12-,14-,15+,16-,18-,19-,20-,21-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C21H26F2O6
Molecular Weight	412.4243
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	9 / 9
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://clinicaltrials.gov/ct2/show/NCT01743690

Fluocinolone participated in clinical trials for the treatment of Oral Lichen Planus and Candida Infection.

Approval Year

PubMed

PubMed

Title	Date	PubMed
Adverse effect of topical fluorinated corticosteroids in rosacea.	1969-03-15	4237682

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 17:52:49 GMT 2025` Edited by `admin` on `Mon Mar 31 17:52:49 GMT 2025`
Record UNII	CT1IX58L9S
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

16.ALPHA.-HYDROXY-6.ALPHA.,9-DIFLUOROPREDNISOLONE

Preferred Name

English

FLUOCINOLONE

Common Name

English

6.ALPHA.-FLUOROTRIAMCINOLONE

Common Name

English

PREGNA-1,4-DIENE-3,20-DIONE, 6.ALPHA.,9-DIFLUORO-11.BETA.,16.ALPHA.,17,21-TETRAHYDROXY-

Systematic Name

English

FLUOCINOLONE [VANDF]

Common Name

English

PREGNA-1,4-DIENE-3,20-DIONE, 6,9-DIFLUORO-11,16,17,21-TETRAHYDROXY-, (6.ALPHA.,11.BETA.,16.ALPHA.)-

Systematic Name

English

FLUOCINOLONE ACETONIDE IMPURITY C [EP IMPURITY]

Common Name

English

Classification Tree Code System Code

CFR

21 CFR 524.981C

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

FDA ORPHAN DRUG

132800

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

NCI_THESAURUS

C521

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

CFR

21 CFR 524.981B

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

CFR

21 CFR 524.981A

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

CFR

21 CFR 524.981D

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

CFR

21 CFR 524.981E

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

Code System Code Type Description

CAS

807-38-5

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

PRIMARY

RXCUI

25126

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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RxNorm

ECHA (EC/EINECS)

212-362-9

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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EPA CompTox

DTXSID001016494

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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LACTMED

Fluocinolone

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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SMS_ID

100000086881

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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WIKIPEDIA

Fluocinolone

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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EVMPD

SUB22923

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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NCI_THESAURUS

C29053

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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ChEMBL

CHEMBL989

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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MESH

C035394

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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FDA UNII

CT1IX58L9S

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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DRUG BANK

DB12553

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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PUBCHEM

91488

Created by admin on Mon Mar 31 17:52:49 GMT 2025 , Edited by admin on Mon Mar 31 17:52:49 GMT 2025

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