CHEBI:133250 - 5-chloromuconolactone(1−)

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ChEBI Name 5-chloromuconolactone(1−)
ChEBI ID CHEBI:133250
ChEBI ASCII Name 5-chloromuconolactone(1-)
Definition A monocarboxylic acid anion that is the conjugate base of 5-chloromuconolactone, obtained by deprotonation of the carboxy group; major species at pH 7.3.
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Gemma Holliday
Supplier Information
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Formula C6H4ClO4
Net Charge -1
Average Mass 175.547
Monoisotopic Mass 174.98036
InChI InChI=1S/C6H5ClO4/c7-5(6(9)10)3-1-2-4(8)11-3/h1-3,5H,(H,9,10)/p-1
InChIKey KGCZGOVWTWDEQD-UHFFFAOYSA-M
SMILES O1C(C=CC1C(C([O-])=O)Cl)=O
Metabolite of Species Details
Rhodococcus opacus (NCBI:txid37919) See: PubMed
Roles Classification
Biological Role(s): bacterial xenobiotic metabolite
Any bacterial metabolite produced by metabolism of a xenobiotic compound in bacteria.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-chloromuconolactone(1−) (CHEBI:133250) has role bacterial xenobiotic metabolite (CHEBI:76976)
5-chloromuconolactone(1−) (CHEBI:133250) is a monocarboxylic acid anion (CHEBI:35757)
5-chloromuconolactone(1−) (CHEBI:133250) is conjugate base of 5-chloromuconolactone (CHEBI:134415)
Incoming 5-chloromuconolactone (CHEBI:134415) is conjugate acid of 5-chloromuconolactone(1−) (CHEBI:133250)
Synonyms Sources
5-chloromuconolactone anion ChEBI
chloro(5-oxo-2,5-dihydrofuran-2-yl)acetate ChEBI
Registry Number Type Source
25133429 Reaxys Registry Number Reaxys
Citation Waiting for Citations Type Source
12218013 PubMed citation SUBMITTER
Last Modified
06 February 2017