CHEBI:4510 - diclofop-methyl

ChEBI IDCHEBI:4510
ChEBI Namediclofop-methyl
Stars
DefinitionA racemate composed of equimolar amounts of (R)- and (S)-diclofop-methyl. A proherbicide for diclofop, it is used for the control of wild oats and annual weeds in wheat, barley, rye and broad-leaved crops.
Last Modified18 November 2019
FormulaC16H14Cl2O4
Net Charge0
Average Mass341.180
Monoisotopic Mass340.02691
Roles Classification
Biological Role:
EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitor  An EC 6.4.1.* (CC bond-forming ligase) inhibitor that interferes with the action of acetyl-CoA carboxylase (EC 6.4.1.2).
Application:
proherbicide  A compound that, on administration, must undergo chemical conversion by biochemical (enzymatic), chemical (possibly following an enzymatic step), or physical (e.g. photochemical) activation processes before becoming the pharmacologically active herbicide for which it is a proherbicide.
ChEBI Ontology
Outgoing Relation(s)
diclofop-methyl (CHEBI:4510) has functional parent diclofop (CHEBI:81909)
diclofop-methyl (CHEBI:4510) has part (R)-diclofop-methyl (CHEBI:145413)
diclofop-methyl (CHEBI:4510) has part (S)-diclofop-methyl (CHEBI:145414)
diclofop-methyl (CHEBI:4510) has role EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitor (CHEBI:70722)
diclofop-methyl (CHEBI:4510) has role proherbicide (CHEBI:136646)
diclofop-methyl (CHEBI:4510) is a racemate (CHEBI:60911)
IUPAC Name 
rac-methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate
Synonyms  Source
diclofop methylKEGG COMPOUND
HOE 23408ChemIDplus
diclofop methyl esterChemIDplus
(±)-diclofop-methylChemIDplus
dichlorfop-methylChemIDplus
methyldiclofopChemIDplus
Brand Names  Source
HoelonChemIDplus
HoegrassChemIDplus
IlloxanChemIDplus
Manual XrefsDatabases
C11021KEGG COMPOUND
221PPDB
DB13918DrugBank
diclofop-methylAlan Wood's Pesticides
Registry NumbersSources
Reaxys:2224754Reaxys
CAS:51338-27-3ChemIDplus
CAS:51338-27-3NIST Chemistry WebBook
Citations