FLUOROMETHOLONE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C22H29FO4
Molecular Weight	376.4617
Optical Activity	UNSPECIFIED
Defined Stereocenters	8 / 8
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of FLUOROMETHOLONE

Structure Search

SMILES

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

InChI

InChIKey=FAOZLTXFLGPHNG-KNAQIMQKSA-N

InChI=1S/C22H29FO4/c1-12-9-17-15-6-8-21(27,13(2)24)20(15,4)11-18(26)22(17,23)19(3)7-5-14(25)10-16(12)19/h5,7,10,12,15,17-18,26-27H,6,8-9,11H2,1-4H3/t12-,15-,17-,18-,19-,20-,21-,22-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C22H29FO4
Molecular Weight	376.4617
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	8 / 8
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 16:04:21 UTC 2023` Edited by `admin` on `Sat Dec 16 16:04:21 UTC 2023`
Record UNII	SV0CSG527L
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

FLUOROMETHOLONE

Official Name

English

FML

Brand Name

English

fluorometholone [INN]

Common Name

English

FLUOROMETHOLONE COMPONENT OF FML-S

Common Name

English

FLUOROMETHOLONE [MI]

Common Name

English

OXYLONE

Brand Name

English

FLUOROMETHOLONE [VANDF]

Common Name

English

9-Fluoro-11β,17-dihydroxy-6α-methylpregna-1,4-diene-3,20-dione

Systematic Name

English

Fluorometholone [WHO-DD]

Common Name

English

PREGNA-1,4-DIENE-3,20-DIONE, 9-FLUORO-11,17-DIHYDROXY-6-METHYL-, (6.ALPHA.,11.BETA.)-

Systematic Name

English

FLUOR-OP

Brand Name

English

FML-S COMPONENT FLUOROMETHOLONE

Common Name

English

NSC-33001

Code

English

FLUOROMETHOLONE [USP-RS]

Common Name

English

FLUOROMETHOLONE [USP MONOGRAPH]

Common Name

English

FLUOROMETHOLONE [JAN]

Common Name

English

FLUOROMETHOLONE [ORANGE BOOK]

Common Name

English

FLUOROMETHOLONE [MART.]

Common Name

English

Classification Tree Code System Code

NDF-RT

N0000175450

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

NDF-RT

N0000175576

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QD07AB06

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

NCI_THESAURUS

C521

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

C05AA06

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

D07AB06

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QC05AA06

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QD07XB04

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

D10AA01

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

S01CA07

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QS01BA07

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

D07CB03

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QS01CB05

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

S01BB03

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QD07CB03

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QS01BB03

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QD10AA01

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-VATC

QS01CA07

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

S01BA07

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

D07XB04

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

WHO-ATC

S01CB05

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

Code System Code Type Description

NCI_THESAURUS

C29058

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

FDA UNII

SV0CSG527L

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

WIKIPEDIA

FLUOROMETHOLONE

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

DRUG BANK

DB00324

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

IUPHAR

7079

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

MERCK INDEX

m5477

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

Merck Index

EVMPD

SUB07720MIG

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

DRUG CENTRAL

1208

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

RXCUI

4491

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

RxNorm

RS_ITEM_NUM

1278007

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

ECHA (EC/EINECS)

207-041-5

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

LACTMED

Fluorometholone

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

CAS

426-13-1

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

SMS_ID

100000091928

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

PUBCHEM

9878

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

DAILYMED

SV0CSG527L

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

EPA CompTox

DTXSID7047435

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

ChEMBL

CHEMBL1200600

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

CHEBI

31625

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

NSC

33001

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

MESH

D005469

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

INN

803

Created by admin on Sat Dec 16 16:04:22 UTC 2023 , Edited by admin on Sat Dec 16 16:04:22 UTC 2023

PRIMARY

Related Record Type Details


					FZW85LW99M

GLUCOCORTICOID RECEPTOR

TARGET -> AGONIST

Related Record Type Details


					9I50C3I3OK

FLUOROMETHOLONE ACETATE

PARENT -> IMPURITY

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

USP

Amount:


					VLK4VG0YDQ

IMPURITY -> PARENT

Interaction Type:

CHROMATOGRAPHIC PURITY (HPLC/UV)

Qualification:

USP

Amount:

Related Record Type Details


					SV0CSG527L

FLUOROMETHOLONE

ACTIVE MOIETY