U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C15H13FO2
Molecular Weight 244.2609
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLURBIPROFEN

SMILES

CC(C(O)=O)C1=CC(F)=C(C=C1)C2=CC=CC=C2

InChI

InChIKey=SYTBZMRGLBWNTM-UHFFFAOYSA-N
InChI=1S/C15H13FO2/c1-10(15(17)18)12-7-8-13(14(16)9-12)11-5-3-2-4-6-11/h2-10H,1H3,(H,17,18)

HIDE SMILES / InChI

Molecular Formula C15H13FO2
Molecular Weight 244.2609
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:20:28 UTC 2023
Edited
by admin
on Fri Dec 15 15:20:28 UTC 2023
Record UNII
5GRO578KLP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLURBIPROFEN
EP   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
flurbiprofen [INN]
Common Name English
BTS 18,322
Code English
FLURBIPROFEN [USP MONOGRAPH]
Common Name English
FLURBIPROFEN [MART.]
Common Name English
FLURBIPROFEN [USAN]
Common Name English
FLURBIPROFEN [ORANGE BOOK]
Common Name English
(±)-2-(2-FLUORO-4-BIPHENYLYL)PROPIONIC ACID
Systematic Name English
FLURBIPROFEN [MI]
Common Name English
FLURBIPROFEN [VANDF]
Common Name English
(1,1'-BIPHENYL)-4-ACETIC ACID, 2-FLUORO-.ALPHA.-METHYL-, (±)-
Systematic Name English
Flurbiprofen [WHO-DD]
Common Name English
NSC-757037
Code English
FLURBIPROFEN [EP MONOGRAPH]
Common Name English
BTS-18322
Code English
U-27,182
Code English
FLURBIPROFEN [JAN]
Common Name English
(±)-2-FLUORO-.ALPHA.-METHYL-4-BIPHENYLACETIC ACID
Systematic Name English
ANSAID
Brand Name English
FLURBIPROFEN [USP-RS]
Common Name English
U-27182
Code English
Classification Tree Code System Code
WHO-VATC QM01AE09
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-VATC QR02AX01
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
NCI_THESAURUS C29577
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-ATC M01AE09
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
NDF-RT N0000175721
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
NCI_THESAURUS C1323
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-VATC QS01BC04
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
NDF-RT N0000000160
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-ATC M02AA19
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-ATC S01BC04
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
NDF-RT N0000175722
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-VATC QM02AA19
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
WHO-ATC R02AX01
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
LIVERTOX NBK548121
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
Code System Code Type Description
ECHA (EC/EINECS)
225-827-6
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
CHEBI
42446
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
DRUG BANK
DB00712
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
CAS
5104-49-4
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
RXCUI
4502
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY RxNorm
NSC
757037
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
IUPHAR
4194
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
EVMPD
SUB07745MIG
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
CHEBI
5130
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
RS_ITEM_NUM
1285750
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
INN
3220
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
SMS_ID
100000092659
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
MERCK INDEX
m5499
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY Merck Index
PUBCHEM
3394
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
EPA CompTox
DTXSID0037231
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
NCI_THESAURUS
C508
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
LACTMED
Flurbiprofen
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
MESH
D005480
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
FDA UNII
5GRO578KLP
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
DRUG CENTRAL
1219
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
WIKIPEDIA
FLURBIPROFEN
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
ChEMBL
CHEMBL563
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
DAILYMED
5GRO578KLP
Created by admin on Fri Dec 15 15:20:29 UTC 2023 , Edited by admin on Fri Dec 15 15:20:29 UTC 2023
PRIMARY
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ENANTIOMER -> RACEMATE
TRANSPORTER -> INHIBITOR
ENANTIOMER -> RACEMATE
DERIVATIVE -> PARENT
METABOLIC ENZYME -> SUBSTRATE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
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METABOLIC ENZYME -> INDUCER
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IMPURITY -> PARENT
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IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Related Record Type Details
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC