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Details

Stereochemistry RACEMIC
Molecular Formula C22H18N2O4
Molecular Weight 374.3893
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FAMOXADONE

SMILES

CC1(OC(=O)N(NC2=CC=CC=C2)C1=O)C3=CC=C(OC4=CC=CC=C4)C=C3

InChI

InChIKey=PCCSBWNGDMYFCW-UHFFFAOYSA-N
InChI=1S/C22H18N2O4/c1-22(16-12-14-19(15-13-16)27-18-10-6-3-7-11-18)20(25)24(21(26)28-22)23-17-8-4-2-5-9-17/h2-15,23H,1H3

HIDE SMILES / InChI

Molecular Formula C22H18N2O4
Molecular Weight 374.3893
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Environmental impact on vascular development predicted by high-throughput screening.
2011-11
Generation and characterization of isolates of Peronophythora litchii resistant to carboxylic acid amide fungicides.
2010-05
Dissipation and residue of famoxadone in grape and soil.
2010-03
Famoxadone residue and dissipation in watermelon and soil.
2010-02
Multiresidue analysis of pesticides in soil by high-performance liquid chromatography with tandem mass spectrometry.
2009-11-18
Multiresidue determination of 11 new fungicides in grapes and wines by liquid-liquid extraction/clean-up and programmable temperature vaporization injection with analyte protectants/gas chromatography/ion trap mass spectrometry.
2009-08-07
Influence of several fungicides on the antioxidant activity of red wines (var. Monastrell).
2009-08
Comparison of stir bar sorptive extraction and membrane-assisted solvent extraction for the ultra-performance liquid chromatographic determination of oxazole fungicide residues in wines and juices.
2008-06-20
Effect of the use of recent commercial fungicides [under good and critical agricultural practices] on the aroma composition of Monastrell red wines.
2008-06-09
Solid-phase microextraction for the gas chromatography mass spectrometric determination of oxazole fungicides in malt beverages.
2008-06
Removal of famoxadone, fluquinconazole and trifloxystrobin residues in red wines: effects of clarification and filtration processes.
2007-09-01
Rapid gas chromatographic method for the determination of famoxadone, trifloxystrobin and fenhexamid residues in tomato, grape and wine samples.
2007-05-25
Effect of mutations in the cytochrome b ef loop on the electron-transfer reactions of the Rieske iron-sulfur protein in the cytochrome bc1 complex.
2007-02-20
Influence of fungicides on grape yeast content and its evolution in the fermentation.
2007
Removal of pesticides from white wine by the use of fining agents and filtration.
2007
Validation and global uncertainty of a liquid chromatographic with diode array detection method for the screening of azoxystrobin, kresoxim-methyl, trifloxystrobin, famoxadone, pyraclostrobin and fenamidone in grapes and wine.
2006-07-28
Determination of fludioxonil and famoxadone in processed fruits and vegetables by liquid chromatography/electrospray tandem mass spectrometry.
2006-03-11
Residues of the fungicide famoxadone in grapes and its fate during wine production.
2006-03
Effect of dose rate and mixtures of fungicides on selection for QoI resistance in populations of Plasmopara viticola.
2006-02
A comparison of a gas chromatographic with electron-capture detection and a gas chromatographic with mass spectrometric detection screening methods for the analysis of famoxadone in grapes and wines.
2006-01-27
Residue evaluation of famoxadone and trifloxystrobin in cultivated mushrooms.
2006
[Determination of famoxadone residue in oranges by GC].
2005-05
Mechanistic differences in inhibition of ubiquinol cytochrome c reductase by the proximal Qo-site inhibitors famoxadone and methoxyacrylate stilbene.
2005-03-15
Architecture of the Qo site of the cytochrome bc1 complex probed by superoxide production.
2003-06-03
Effect of famoxadone on photoinduced electron transfer between the iron-sulfur center and cytochrome c1 in the cytochrome bc1 complex.
2003-03-28
The crystal structure of mitochondrial cytochrome bc1 in complex with famoxadone: the role of aromatic-aromatic interaction in inhibition.
2002-10-01
Sensitivity of mitochondrial respiration to different inhibitors in Venturia inaequalis.
2001-09
Famoxadone: the discovery and optimisation of a new agricultural fungicide.
2001-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:27:56 GMT 2025
Edited
by admin
on Mon Mar 31 22:27:56 GMT 2025
Record UNII
V1C07OR6II
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FAMOXADONE
ISO   MI  
Common Name English
DPX-JE 874
Preferred Name English
FAMOXADONE [ISO]
Common Name English
FAMOXATE [HSDB]
Common Name English
5-METHYL-5-(4-PHENOXYPHENYL)-3-(PHENYLAMINO)-2,4-OXAZOLIDINEDIONE
Systematic Name English
FAMOXADONE [MI]
Common Name English
2,4-OXAZOLIDINEDIONE, 5-METHYL-5-(4-PHENOXYPHENYL)-3- (PHENYLAMINO)-
Systematic Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 113202
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
Code System Code Type Description
MERCK INDEX
m5242
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY Merck Index
PUBCHEM
213032
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
WIKIPEDIA
Famoxadone
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
ALANWOOD
famoxadone
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
CAS
131807-57-3
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
HSDB
7266
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID8034588
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
CHEBI
59340
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY
FDA UNII
V1C07OR6II
Created by admin on Mon Mar 31 22:27:56 GMT 2025 , Edited by admin on Mon Mar 31 22:27:56 GMT 2025
PRIMARY