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
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)
| 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 | ( + / - ) |
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Pharmacokinetics and pharmacodynamics of fenleuton, a 5-lipoxygenase inhibitor, in ponies. | 1998-06-13 |
|
| Effect of the 5-lipoxygenase inhibitor, fenleuton, on antigen-induced neutrophil accumulation and lung function changes in horses with chronic obstructive pulmonary disease. | 1998-06 |
|
| Dietary fish oil or lofrin, a 5-lipoxygenase inhibitor, decrease the growth-suppressing effects of coccidiosis in broiler chicks. | 1997-10 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:32:33 GMT 2025
by
admin
on
Mon Mar 31 18:32:33 GMT 2025
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| Record UNII |
LG64454O6I
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C1322
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72059
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DTXSID40869916
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GG-24
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SUB07570MIG
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141579-54-6
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C65656
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LG64454O6I
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100000081278
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Fenleuton
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CHEMBL293743
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7321
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PRIMARY |
| Related Record | Type | Details | ||
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ENANTIOMER -> RACEMATE | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
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ACTIVE MOIETY |