CHEBI:29806 - fumarate(2−)

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ChEBI Name fumarate(2−)
ChEBI ID CHEBI:29806
ChEBI ASCII Name fumarate(2-)
Definition A C4-dicarboxylate that is the E-isomer of but-2-enedioate(2−)
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:24122, CHEBI:42511, CHEBI:14284
Supplier Information
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Formula C4H2O4
Net Charge -2
Average Mass 114.05628
Monoisotopic Mass 113.99641
InChI InChI=1S/C4H4O4/c5-3(6)1-2-4(7)8/h1-2H,(H,5,6)(H,7,8)/p-2/b2-1+
InChIKey VZCYOOQTPOCHFL-OWOJBTEDSA-L
SMILES [O-]C(=O)\C=C\C([O-])=O
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing fumarate(2−) (CHEBI:29806) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
fumarate(2−) (CHEBI:29806) has role human metabolite (CHEBI:77746)
fumarate(2−) (CHEBI:29806) has role metabolite (CHEBI:25212)
fumarate(2−) (CHEBI:29806) is a butenedioate (CHEBI:36180)
fumarate(2−) (CHEBI:29806) is a C4-dicarboxylate (CHEBI:61336)
fumarate(2−) (CHEBI:29806) is conjugate base of fumarate(1−) (CHEBI:37154)
Incoming dihydroxyfumarate(2−) (CHEBI:17795) has functional parent fumarate(2−) (CHEBI:29806)
mesaconate(2−) (CHEBI:36986) has functional parent fumarate(2−) (CHEBI:29806)
disodium fumarate (CHEBI:115156) has part fumarate(2−) (CHEBI:29806)
fumarate(1−) (CHEBI:37154) is conjugate acid of fumarate(2−) (CHEBI:29806)
IUPAC Name
(2E)-but-2-enedioate
Synonyms Sources
(2E)-but-2-enedioate ChEBI
(E)-2-butenedioic acid, ion(2−) ChemIDplus
FUMARATE PDBeChem
fumarate UniProt
Manual Xrefs Databases
C00122 KEGG COMPOUND
c0111 UM-BBD
DB01677 DrugBank
FUM PDBeChem
FUM MetaCyc
View more database links
Registry Numbers Types Sources
142-42-7 CAS Registry Number ChemIDplus
1861276 Beilstein Registry Number Beilstein
1861276 Reaxys Registry Number Reaxys
325288 Gmelin Registry Number Gmelin
Citations Waiting for Citations Types Sources
15618158 PubMed citation Europe PMC
16857679 PubMed citation Europe PMC
17190852 PubMed citation Europe PMC
22052553 PubMed citation Europe PMC
22405071 PubMed citation Europe PMC
Last Modified
20 November 2019