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Details

Stereochemistry ACHIRAL
Molecular Formula C11H11F3N2O3
Molecular Weight 276.2118
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FLUTAMIDE

SMILES

CC(C)C(=O)NC1=CC(=C(C=C1)[N+]([O-])=O)C(F)(F)F

InChI

InChIKey=MKXKFYHWDHIYRV-UHFFFAOYSA-N
InChI=1S/C11H11F3N2O3/c1-6(2)10(17)15-7-3-4-9(16(18)19)8(5-7)11(12,13)14/h3-6H,1-2H3,(H,15,17)

HIDE SMILES / InChI
Molecular Formula C11H11F3N2O3
Molecular Weight 276.2118
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
123738
Substance Class Chemical
Created
by admin
on Sat Dec 16 17:43:06 UTC 2023
Edited
by admin
on Sat Dec 16 17:43:06 UTC 2023
Record UNII
76W6J0943E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FLUTAMIDE
EP   INN   JAN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
USAN   INN  
Official Name English
NSC-215876
Code English
FLUTAMIDE [EP IMPURITY]
Common Name English
FLUTAMIDE [EP MONOGRAPH]
Common Name English
FLUTAMIDE [USAN]
Common Name English
EULEXIN
Brand Name English
FLUTAMIDE [MART.]
Common Name English
FLUTAMIDE [ORANGE BOOK]
Common Name English
SCH-13521
Code English
PROPANAMIDE, 2-METHYL-N-(4-NITRO-3-(TRIFLUOROMETHYL)PHENYL)-
Systematic Name English
SCH 13521
Code English
.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-2-METHYL-4'-NITRO-M-PROPIONOTOLUIDIDE
Common Name English
FLUTAMIDE [USP-RS]
Common Name English
FLUTAMIDE [MI]
Common Name English
Flutamide [WHO-DD]
Common Name English
FLUTAMIDE [USP MONOGRAPH]
Common Name English
FLUTAMIDE [JAN]
Common Name English
flutamide [INN]
Common Name English
Classification Tree Code System Code
NDF-RT N0000175560
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
WHO-ATC L02BB01
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
NDF-RT N0000000243
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
NCI_THESAURUS C242
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
NCI_THESAURUS C1915
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
WHO-VATC QL02BB01
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
LIVERTOX NBK548908
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
Code System Code Type Description
DAILYMED
76W6J0943E
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
WIKIPEDIA
FLUTAMIDE
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
DRUG BANK
DB00499
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
RS_ITEM_NUM
1285851
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
CHEBI
5132
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
MERCK INDEX
m5508
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL806
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
RXCUI
4508
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
236-341-9
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
SMS_ID
100000092094
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
CAS
13311-84-7
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
DRUG CENTRAL
1223
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
INN
3483
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
PUBCHEM
3397
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
MESH
D005485
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
IUPHAR
6943
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
FDA UNII
76W6J0943E
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
EPA CompTox
DTXSID7032004
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
NCI_THESAURUS
C509
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
NSC
215876
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
EVMPD
SUB07756MIG
Created by admin on Sat Dec 16 17:43:07 UTC 2023 , Edited by admin on Sat Dec 16 17:43:07 UTC 2023
PRIMARY
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MRP-1
TRANSPORTER -> SUBSTRATE
Structure of FLUTAMIDE
BASIS OF STRENGTH->SUBSTANCE
ASSAY (UV)
EP
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BINDER->LIGAND
Structure of FLUTAMIDE
BASIS OF STRENGTH->SUBSTANCE
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ANDROGEN RECEPTOR
TARGET -> INHIBITOR
BINDING
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Structure of 2-AMINO-5-NITRO-4-(TRIFLUOROMETHYL)PHENOL
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Structure of 2-AMINO-5-NITRO-4-(TRIFLUOROMETHYL)PHENOL, O-GLUCURONIDE
METABOLITE -> PARENT
URINE
Structure of 2-AMINO-5-NITRO-4-(TRIFLUOROMETHYL)PHENOL, 1-(HYDROGEN SULFATE)
METABOLITE -> PARENT
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IMPURITY -> PARENT
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Structure of 3-TRIFLUOROMETHYLISOBUTYRANILIDE
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Structure of 3-TRIFLUOROMETHYLANILINE
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Structure of 4-NITRO-3-TRIFLUOROMETHYLPROPIONANILIDE
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Structure of 4-NITRO-3-TRIFLUOROMETHYLACETANILIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Structure of 3-TRIFLUOROMETHYLANILINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-NITRO-3-TRIFLUOROMETHYLANILINE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Structure of O-FLUTAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
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Structure of 4-NITRO-3-TRIFLUOROMETHYLACETANILIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-NITRO-3-TRIFLUOROMETHYLPROPIONANILIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 3-TRIFLUOROMETHYLISOBUTYRANILIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of FLUTAMIDE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC
Tmax PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
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