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InChI=1S/CH4O/c1-2/h2H,1H3
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ChEBI
> Main
CHEBI:15740 - formate
Main
ChEBI Ontology
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ChEBI Name
formate
ChEBI ID
CHEBI:15740
Definition
A monocarboxylic acid anion that is the conjugate base of formic acid. Induces severe metabolic acidosis and ocular injury in human subjects.
Stars
This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs
CHEBI:14276, CHEBI:24081
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Formula
CHO2
Net Charge
-1
Average Mass
45.01744
Monoisotopic Mass
44.99820
InChI
InChI=1S/CH2O2/c2-1-3/h1H,(H,2,3)/p-1
InChIKey
BDAGIHXWWSANSR-UHFFFAOYSA-M
SMILES
[H]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
).
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (
Homo sapiens
).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing
formate (
CHEBI:15740
)
has role
Saccharomyces cerevisiae
metabolite (
CHEBI:75772
)
formate (
CHEBI:15740
)
has role
human metabolite (
CHEBI:77746
)
formate (
CHEBI:15740
)
is a
monocarboxylic acid anion (
CHEBI:35757
)
formate (
CHEBI:15740
)
is conjugate base of
formic acid (
CHEBI:30751
)
Incoming
caesium formate (
CHEBI:190475
)
has part
formate (
CHEBI:15740
)
ethylammonium formate (
CHEBI:63880
)
has part
formate (
CHEBI:15740
)
sodium formate (
CHEBI:62965
)
has part
formate (
CHEBI:15740
)
formic acid (
CHEBI:30751
)
is conjugate acid of
formate (
CHEBI:15740
)
carboxylato group (
CHEBI:18245
)
is substituent group from
formate (
CHEBI:15740
)
IUPAC Name
formate
Synonyms
Sources
aminate
ChEBI
formate
UniProt
formiate
ChEBI
formic acid, ion(1−)
ChemIDplus
formylate
ChEBI
HCO2 anion
NIST Chemistry WebBook
hydrogen carboxylate
ChEBI
methanoate
ChEBI
Manual Xrefs
Databases
C00058
KEGG COMPOUND
c0106
UM-BBD
Formate
Wikipedia
FORMATE
MetaCyc
HMDB0000142
HMDB
View more database links
Registry Numbers
Types
Sources
1006
Gmelin Registry Number
Gmelin
1901205
Reaxys Registry Number
Reaxys
1901205
Beilstein Registry Number
Beilstein
71-47-6
CAS Registry Number
NIST Chemistry WebBook
71-47-6
CAS Registry Number
ChemIDplus
Citations
Types
Sources
17190852
PubMed citation
Europe PMC
3946945
PubMed citation
Europe PMC
Last Modified
31 March 2022