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

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
Effect of famoxadone on photoinduced electron transfer between the iron-sulfur center and cytochrome c1 in the cytochrome bc1 complex.
2003 Mar 28
Effect of dose rate and mixtures of fungicides on selection for QoI resistance in populations of Plasmopara viticola.
2006 Feb
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
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 Feb 20
Rapid gas chromatographic method for the determination of famoxadone, trifloxystrobin and fenhexamid residues in tomato, grape and wine samples.
2007 May 25
Influence of several fungicides on the antioxidant activity of red wines (var. Monastrell).
2009 Aug
Multiresidue analysis of pesticides in soil by high-performance liquid chromatography with tandem mass spectrometry.
2009 Sep-Oct
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 09:04:02 GMT 2023
Edited
by admin
on Sat Dec 16 09:04:02 GMT 2023
Record UNII
V1C07OR6II
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FAMOXADONE
ISO   MI  
Common 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
DPX-JE 874
Brand 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 Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
Code System Code Type Description
MERCK INDEX
m5242
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY Merck Index
PUBCHEM
213032
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
WIKIPEDIA
Famoxadone
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
ALANWOOD
famoxadone
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
CAS
131807-57-3
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
HSDB
7266
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
EPA CompTox
DTXSID8034588
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
CHEBI
59340
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY
FDA UNII
V1C07OR6II
Created by admin on Sat Dec 16 09:04:02 GMT 2023 , Edited by admin on Sat Dec 16 09:04:02 GMT 2023
PRIMARY