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InChI=1S/CH4O/c1-2/h2H,1H3
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> Main
CHEBI:30845 - 2-furoic acid
Main
ChEBI Ontology
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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
Supplier Information
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Read full article at Wikipedia
Formula
C5H4O3
Net Charge
0
Average Mass
112.084
Monoisotopic Mass
112.01604
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)C1=CC=CO1
Metabolite of Species
Details
Cordyceps sinensis
(NCBI:txid72228)
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 (Br
o
nsted 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
)
2-Phenylethyl 2-furancarboxylate (
CHEBI:174094
)
has functional parent
2-furoic acid (
CHEBI:30845
)
2-Propenyl 2-furancarboxylate (
CHEBI:173650
)
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-Bromopyridin-3-yl furan-2-carboxylate (
CHEBI:149861
)
has functional parent
2-furoic acid (
CHEBI:30845
)
5-Chloro-3-pyridinyl 2-furoate (
CHEBI:149866
)
has functional parent
2-furoic acid (
CHEBI:30845
)
5-Chloropyridin-3-yl 5-(4-chlorophenyl)furan-2-carboxylate (
CHEBI:149865
)
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
)
[(1
R
)-1-{[
N
-(furan-2-ylcarbonyl)-
L
-leucyl]amino}-2-(1
H
-indol-3-yl)ethyl]phosphonic acid (
CHEBI:42450
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Amyl 2-furoate (
CHEBI:172428
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Asperfuran A (
CHEBI:213814
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Dimethyl 3,4-dihydroxyfuran-2,5-dicarboxylate (
CHEBI:189133
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Epoxydine B (
CHEBI:216947
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Ethyl 2-phenyl-3-furancarboxylate (
CHEBI:174095
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Ethyl 3-furoate (
CHEBI:193961
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Ethyl furoate (
CHEBI:169174
)
has functional parent
2-furoic acid (
CHEBI:30845
)
GNF5343 (
CHEBI:133823
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Hexyl 2-furoate (
CHEBI:169465
)
has functional parent
2-furoic acid (
CHEBI:30845
)
HS071 (
CHEBI:197907
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Isoamyl 2-furoate (
CHEBI:179565
)
has functional parent
2-furoic acid (
CHEBI:30845
)
LSM-26546 (
CHEBI:115084
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Methyl 2-Furancarboxylate (
CHEBI:167081
)
has functional parent
2-furoic acid (
CHEBI:30845
)
methyl 5-(hydroxymethyl) furan-2-carboxylate (
CHEBI:204914
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Methyl 5-nitro-2-furoate (
CHEBI:189109
)
has functional parent
2-furoic acid (
CHEBI:30845
)
methyl 5-{[2-(ethoxycarbonyl)-3-oxohex-1-enyl]amino}-2-furoate (
CHEBI:183376
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Octyl 2-furoate (
CHEBI:174156
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Propyl 2-furoate (
CHEBI:173659
)
has functional parent
2-furoic acid (
CHEBI:30845
)
Robillafuran (
CHEBI:226687
)
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
Manual Xrefs
Databases
10251740
ChemSpider
2-Furoic_acid
Wikipedia
C00000151
KNApSAcK
C01546
KEGG COMPOUND
FDB000951
FooDB
FOA
PDBeChem
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
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
26378464
PubMed citation
Europe PMC
29097752
PubMed citation
Europe PMC
Last Modified
28 May 2021
General Comments
2011-05-19
A metabolite marker of exposure to the common industrial solvent furfural.
2011-05-19
A known biomass inhibitor.