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Details

Stereochemistry RACEMIC
Molecular Formula C17H15FN2O3
Molecular Weight 314.311
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FENLEUTON

SMILES

CC(C#CC1=CC(OC2=CC=C(F)C=C2)=CC=C1)N(O)C(N)=O

InChI

InChIKey=MWXPQCKCKPYBDR-UHFFFAOYSA-N
InChI=1S/C17H15FN2O3/c1-12(20(22)17(19)21)5-6-13-3-2-4-16(11-13)23-15-9-7-14(18)8-10-15/h2-4,7-12,22H,1H3,(H2,19,21)

HIDE SMILES / InChI

Molecular Formula C17H15FN2O3
Molecular Weight 314.311
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

FENLEUTON is a potent, reversible and selective inhibitor of 5-lipoxygenase with IC50 values ranging from 80 to 1100 nM. It was studied for potential use in veterinary medicine to treat chronic obstructive pulmonary disease in horses.

Approval Year

PubMed

PubMed

TitleDatePubMed
Dietary fish oil or lofrin, a 5-lipoxygenase inhibitor, decrease the growth-suppressing effects of coccidiosis in broiler chicks.
1997 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:36:45 UTC 2023
Edited
by admin
on Fri Dec 15 16:36:45 UTC 2023
Record UNII
LG64454O6I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FENLEUTON
INN   USAN  
USAN   INN  
Official Name English
N-HYDROXY-N-(4-(3-(4-FLUOROPHENOXY)PHENYL)-3-BUTYN-2-YL)UREA
Systematic Name English
ABBOTT-76745
Code English
fenleuton [INN]
Common Name English
UREA, N-(3-(3-(4-FLUOROPHENOXY)PHENYL)-1-METHYL-2-PROPYNYL)-N-HYDROXY-
Systematic Name English
FENLEUTON [USAN]
Common Name English
UREA, N-(3-(3-(4-FLUOROPHENOXY)PHENYL)-1-METHYL-2-PROPYNYL)-N-HYDROXY-, (±)-
Systematic Name English
LOFRIN
Brand Name English
A-76745
Code English
UREA, N-(3-(3-(4-FLUOROPHENOXY)PHENYL)-1-METHYL-2-PROPYN-1-YL)-N-HYDROXY-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C1322
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
Code System Code Type Description
PUBCHEM
72059
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
EPA CompTox
DTXSID40869916
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
USAN
GG-24
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
EVMPD
SUB07570MIG
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
CAS
141579-54-6
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
NCI_THESAURUS
C65656
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
FDA UNII
LG64454O6I
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
SMS_ID
100000081278
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
WIKIPEDIA
Fenleuton
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
ChEMBL
CHEMBL293743
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
INN
7321
Created by admin on Fri Dec 15 16:36:45 UTC 2023 , Edited by admin on Fri Dec 15 16:36:45 UTC 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY