CHEBI:132841 - clodinafop

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ChEBI Name clodinafop
Definition An aromatic ether that is (R)-lactic acid in which the hydroxy group at position 2 has been converted to the corresponding p-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenyl ether. It is the parent acid of the herbicide clodinafop-propargyl.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Barrie Walker
Supplier Information
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Formula C14H11ClFNO4
Net Charge 0
Average Mass 311.693
Monoisotopic Mass 311.03606
InChI InChI=1S/C14H11ClFNO4/c1-8(14(18)19)20-10-2-4-11(5-3-10)21-13-12(16)6-9(15)7-17-13/h2-8H,1H3,(H,18,19)/t8-/m1/s1
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): EC (acetyl-CoA carboxylase) inhibitor
An EC 6.4.1.* (C1C bond-forming ligase) inhibitor that interferes with the action of acetyl-CoA carboxylase (EC
Application(s): phenoxy herbicide
Any member of the class of herbicides whose members contain a phenoxy or substituted phenoxy group.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing clodinafop (CHEBI:132841) has role EC (acetyl-CoA carboxylase) inhibitor (CHEBI:70722)
clodinafop (CHEBI:132841) has role phenoxy herbicide (CHEBI:60575)
clodinafop (CHEBI:132841) is a aromatic ether (CHEBI:35618)
clodinafop (CHEBI:132841) is a monocarboxylic acid (CHEBI:25384)
clodinafop (CHEBI:132841) is a organochlorine compound (CHEBI:36683)
clodinafop (CHEBI:132841) is a organofluorine compound (CHEBI:37143)
clodinafop (CHEBI:132841) is a pyridines (CHEBI:26421)
Incoming clodinafop-propargyl (CHEBI:132921) has functional parent clodinafop (CHEBI:132841)
(2R)-2-{4-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenoxy}propanoic acid
Synonyms Sources
(2R)-2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]propanoic acid SUBMITTER
(R)-2-[4-(5-chloro-3-fluoro-2-pyridyloxy)phenoxy]propionic acid SUBMITTER
(R)-2-{4-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenoxy}propionic acid SUBMITTER
Manual Xrefs Databases
1416 PPDB
clodinafop Alan Wood's Pesticides
View more database links
Registry Numbers Types Sources
10562170 Reaxys Registry Number Reaxys
10562170 Beilstein Registry Number Beilstein
114420-56-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
10557330 PubMed citation Europe PMC
16047877 PubMed citation Europe PMC
16977528 PubMed citation Europe PMC
19290455 PubMed citation Europe PMC
19594140 PubMed citation Europe PMC
19756846 PubMed citation Europe PMC
19784963 PubMed citation Europe PMC
24121741 PubMed citation Europe PMC
26065513 PubMed citation Europe PMC
IND43870723 Agricola citation Europe PMC
IND44076496 Agricola citation Europe PMC
Last Modified
18 November 2019