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Details

Stereochemistry ACHIRAL
Molecular Formula C15H10ClF3N2O6S
Molecular Weight 438.763
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FOMESAFEN

SMILES

CS(=O)(=O)NC(=O)C1=C(C=CC(OC2=C(Cl)C=C(C=C2)C(F)(F)F)=C1)[N+]([O-])=O

InChI

InChIKey=BGZZWXTVIYUUEY-UHFFFAOYSA-N
InChI=1S/C15H10ClF3N2O6S/c1-28(25,26)20-14(22)10-7-9(3-4-12(10)21(23)24)27-13-5-2-8(6-11(13)16)15(17,18)19/h2-7H,1H3,(H,20,22)

HIDE SMILES / InChI

Molecular Formula C15H10ClF3N2O6S
Molecular Weight 438.763
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
The effect of protoporphyrinogen oxidase inhibitors on microsomal and mitochondrial cytochromes.
1995 Dec
[Participation of dexamethasone and E and C vitamins in the modulation of the hepatotoxic effect induced by fomesafen and 2,4-D amino herbicides, in rats ].
2002
Nonylphenol polyethoxylate adjuvant mitigates the reproductive toxicity of fomesafen on the freshwater snail Lymnaea stagnalis in outdoor experimental ponds.
2002 Sep
Solid-phase fluoroimmunoassay for the determination of mesotrione--a novel triketone herbicide--in water with direct measurement of the fluorescence onto the solid support.
2003 Apr
ZnCl2 induces Syrian hamster embryo (SHE) cell transformation.
2003 Apr 30
Circadian response of annual weeds in a natural setting to high and low application rates of four herbicides with different modes of actions.
2003 Mar
Experimental hepatic uroporphyria induced by the diphenyl-ether herbicide fomesafen in male DBA/2 mice.
2003 May 15
Quantitative expression analysis of GH3, a gene induced by plant growth regulator herbicides in soybean.
2004 Feb 11
Population dynamics of weeds in no-tillage and conventional crop systems.
2005
Multiple resistance of acetolactate synthase and protoporphyrinogen oxidase inhibitors in Euphorbia heterophylla biotypes.
2005
Homoglutathione confers tolerance to acifluorfen in transgenic tobacco plants expressing soybean homoglutathione synthetase.
2005 Aug
Manipulation of plant tolerance to herbicides through co-ordinated metabolic engineering of a detoxifying glutathione transferase and thiol cosubstrate.
2005 Jul
Effects of fomesafen, alone and in combination with an adjuvant, on plankton communities in freshwater outdoor pond mesocosms.
2005 May
Effects of self-fertilization, environmental stress and exposure to xenobiotics on fitness-related traits of the freshwater snail Lymnaea stagnalis.
2006 Mar
Use of carbon and nitrogen stable isotope ratios to assess the effects of environmental contaminants on aquatic food webs.
2006 May
Hemocyte-specific responses to the peroxidizing herbicide fomesafen in the pond snail Lymnaea stagnalis (Gastropoda, Pulmonata).
2007 Mar
Haemocyte apoptosis as a general cellular immune response of the snail, Lymnaea stagnalis, to a toxicant.
2007 May
Effect of a toxicant on phagocytosis pathways in the freshwater snail Lymnaea stagnalis.
2008 Jul
Biodegradation of fomesafen by strain Lysinibacillus sp. ZB-1 isolated from soil.
2009 Dec
Effects of diquat and fomesafen applied alone and in combination with a nonylphenol polyethoxylate adjuvant on Lemna minor in aquatic indoor microcosms.
2009 Mar
[Isolation, identification and soil remediation of atrazine-degrading strain T3 AB1].
2010 Dec
[Determination of biphenyl ether herbicides in water using HPLC with cloud-point extraction].
2010 Jan
Assessment of possible carcinogenicity of oxyfluorfen to humans using mode of action analysis of rodent liver effects.
2012 Aug
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:53:11 GMT 2023
Edited
by admin
on Fri Dec 15 18:53:11 GMT 2023
Record UNII
M0A3U4CDTF
Record Status Validated (UNII)
Record Version
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Name Type Language
FOMESAFEN
HSDB   ISO   MI  
Common Name English
FOMESAFEN [ISO]
Common Name English
5-(2-CHLORO-.ALPHA.,.ALPHA.,.ALPHA.-TRIFLUORO-P-TOLYLOXY)-N-MESYL-2-NITROBENZAMIDE
Common Name English
FOMESAFEN [MI]
Common Name English
5-(2-CHLORO-4-(TRIFLUOROMETHYL)PHENOXY)-N-(METHYLSULFONYL)-2-NITROBENZAMIDE
Systematic Name English
FOMESAFEN [HSDB]
Common Name English
Classification Tree Code System Code
EPA PESTICIDE CODE 123803
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
Code System Code Type Description
FDA UNII
M0A3U4CDTF
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
MERCK INDEX
m5524
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY Merck Index
PUBCHEM
51556
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
HSDB
6660
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
MESH
C088563
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
ECHA (EC/EINECS)
276-439-9
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
EPA CompTox
DTXSID7024112
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
CAS
72178-02-0
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
WIKIPEDIA
Fomesafen
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY
ALANWOOD
fomesafen
Created by admin on Fri Dec 15 18:53:11 GMT 2023 , Edited by admin on Fri Dec 15 18:53:11 GMT 2023
PRIMARY