CHEBI:30845 - 2-furoic acid

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ChEBI Name 2-furoic acid
ChEBI ID CHEBI:30845
Definition A furoic acid having the carboxylic acid group located at position 2.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:42470, CHEBI:1101, CHEBI:19583
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Formula C5H4O3
Net Charge 0
Average Mass 112.08350
Monoisotopic Mass 112.016
InChI InChI=1S/C5H4O3/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)
InChIKey SMNDYUVBFMFKNZ-UHFFFAOYSA-N
SMILES OC(=O)c1ccco1
Metabolite of Species Details
Cordyceps sinensis (NCBI:72228) Found in mycelium (BTO:0001436). Ethanolic extract of dried mycelia See: PubMed
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): plant metabolite
Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
bacterial xenobiotic metabolite
Any bacterial metabolite produced by metabolism of a xenobiotic compound in bacteria.
human xenobiotic metabolite
Any human metabolite produced by metabolism of a xenobiotic compound in humans.
Saccharomyces cerevisiae metabolite
Any fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae ).
inhibitor
A substance that diminishes the rate of a chemical reaction.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 2-furoic acid (CHEBI:30845) has role Saccharomyces cerevisiae metabolite (CHEBI:75772)
2-furoic acid (CHEBI:30845) has role bacterial xenobiotic metabolite (CHEBI:76976)
2-furoic acid (CHEBI:30845) has role human xenobiotic metabolite (CHEBI:76967)
2-furoic acid (CHEBI:30845) has role inhibitor (CHEBI:35222)
2-furoic acid (CHEBI:30845) has role plant metabolite (CHEBI:76924)
2-furoic acid (CHEBI:30845) is a furoic acid (CHEBI:36055)
2-furoic acid (CHEBI:30845) is conjugate acid of 2-furoate (CHEBI:16739)
Incoming 2-furancarboxylic acid (2-acetyl-1-benzothiophen-3-yl) ester (CHEBI:109645) has functional parent 2-furoic acid (CHEBI:30845)
2-furoate ester (CHEBI:50856) has functional parent 2-furoic acid (CHEBI:30845)
2-furoyl-CoA (CHEBI:15474) has functional parent 2-furoic acid (CHEBI:30845)
4-acetyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid (5-methoxycarbonyl-2-furanyl)methyl ester (CHEBI:123325) has functional parent 2-furoic acid (CHEBI:30845)
5-(tetradecyloxy)-2-furoic acid (CHEBI:77936) has functional parent 2-furoic acid (CHEBI:30845)
5-[[(2-sulfanylidene-3H-1,3,4-thiadiazol-5-yl)thio]methyl]-2-furancarboxylic acid methyl ester (CHEBI:109774) has functional parent 2-furoic acid (CHEBI:30845)
5-[[[(5-tert-butyl-2-methyl-3-furanyl)-oxomethyl]amino]methyl]-2-furancarboxylic acid ethyl ester (CHEBI:121331) has functional parent 2-furoic acid (CHEBI:30845)
5-bromo-2-furancarboxylic acid [2-[1-(2-methoxyethyl)-2,5-dimethyl-3-pyrrolyl]-2-oxoethyl] ester (CHEBI:120887) has functional parent 2-furoic acid (CHEBI:30845)
5-nitro-2-furancarboxylic acid (5-phenyl-1,3,4-oxadiazol-2-yl)methyl ester (CHEBI:95223) has functional parent 2-furoic acid (CHEBI:30845)
N-(2-furoyl)glycine (CHEBI:82912) has functional parent 2-furoic acid (CHEBI:30845)
N-2-furoyl-L-leucine (CHEBI:42477) has functional parent 2-furoic acid (CHEBI:30845)
[(1R)-1-{[N-(furan-2-ylcarbonyl)-L-leucyl]amino}-2-(1H-indol-3-yl)ethyl]phosphonic acid (CHEBI:42450) has functional parent 2-furoic acid (CHEBI:30845)
GNF5343 (CHEBI:133823) has functional parent 2-furoic acid (CHEBI:30845)
LSM-26546 (CHEBI:115084) has functional parent 2-furoic acid (CHEBI:30845)
2-furoate (CHEBI:16739) is conjugate base of 2-furoic acid (CHEBI:30845)
IUPAC Name
furan-2-carboxylic acid
Synonyms Sources
2-carboxyfuran NIST Chemistry WebBook
2-Furancarboxylic acid KEGG COMPOUND
2-furanoic acid ChEBI
2-Furoic acid KEGG COMPOUND
2-FUROIC ACID PDBeChem
2-furoic acid IUPAC
acide 2-furoïque ChEBI
ácido 2-furoico ChEBI
α-furancarboxylic acid NIST Chemistry WebBook
α-furoic acid NIST Chemistry WebBook
Furan-2-carbonsäure ChEBI
Pyromucic acid KEGG COMPOUND
Database Links Databases
2-Furoic_acid Wikipedia
C00000151 KNApSAcK
C01546 KEGG COMPOUND
HMDB0000617 HMDB
View more database links
Registry Numbers Types Sources
110149 Reaxys Registry Number Reaxys
110149 Beilstein Registry Number Beilstein
3056 Gmelin Registry Number Gmelin
88-14-2 CAS Registry Number KEGG COMPOUND
88-14-2 CAS Registry Number NIST Chemistry WebBook
88-14-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
12587683 PubMed citation Europe PMC
16306695 PubMed citation Europe PMC
18492059 PubMed citation Europe PMC
19938546 PubMed citation Europe PMC
20393580 PubMed citation Europe PMC
22031465 PubMed citation Europe PMC
23421908 PubMed citation Europe PMC
Last Modified
26 October 2016
General Comments
2011-05-19 A metabolite marker of exposure to the common industrial solvent furfural.
2011-05-19 A known biomass inhibitor.