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pyruvate (CHEBI:15361)

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ChEBI Name pyruvate
ChEBI ID CHEBI:15361
Definition A 2-oxo monocarboxylic acid anion that is the conjugate base of pyruvic acid, arising from deprotonation of the carboxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:14987, CHEBI:26462
Supplier Information
See structure as:  Image  Applet
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Formula Source
C3H3O3 ChEBI
Net Charge -1
Average Mass 87.05412
InChI
InChI=1S/C3H4O3/c1-2(4)3(5)6/h1H3,(H,5,6)/p-1
InChIKey
LCTONWCANYUPML-UHFFFAOYSA-M
SMILES
CC(=O)C([O-])=O
Metabolite of Species Source
Isolated from Homo sapiens (NCBI:9606) DOI
Roles Classification
Biological Role(s): 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 on the ChEBI Ontology
ChEBI Ontology
Outgoing pyruvate (CHEBI:15361) has functional parent propionate (CHEBI:17272)
pyruvate (CHEBI:15361) has role human metabolite (CHEBI:77746)
pyruvate (CHEBI:15361) has role metabolite (CHEBI:25212)
pyruvate (CHEBI:15361) is a 2-oxo monocarboxylic acid anion (CHEBI:35179)
pyruvate (CHEBI:15361) is conjugate base of pyruvic acid (CHEBI:32816)
Incoming (4-bromophenylsulfanyl)pyruvate (CHEBI:17468) has functional parent pyruvate (CHEBI:15361)
3,4-dihydro-4-hydroxyphenylpyruvate (CHEBI:64788) has functional parent pyruvate (CHEBI:15361)
3,4-dihydroxyphenylpyruvate (CHEBI:29055) has functional parent pyruvate (CHEBI:15361)
3-(4-hydroxycyclohex-2-en-1-ylidene)pyruvate (CHEBI:64789) has functional parent pyruvate (CHEBI:15361)
3-(4-hydroxyphenyl)pyruvate (CHEBI:36242) has functional parent pyruvate (CHEBI:15361)
3-(5-benzyloxyindol-3-yl)pyruvate (CHEBI:55520) has functional parent pyruvate (CHEBI:15361)
3-acylpyruvate (CHEBI:57278) has functional parent pyruvate (CHEBI:15361)
3-dimethylallyl-4-hydroxyphenylpyruvate(1−) (CHEBI:74408) has functional parent pyruvate (CHEBI:15361)
3-fluoropyruvate (CHEBI:55522) has functional parent pyruvate (CHEBI:15361)
3-hydroxypyruvate (CHEBI:17180) has functional parent pyruvate (CHEBI:15361)
3-phosphonatooxypyruvate(3−) (CHEBI:18110) has functional parent pyruvate (CHEBI:15361)
3-phosphonatopyruvate(2−) (CHEBI:71402) has functional parent pyruvate (CHEBI:15361)
3-phosphonatopyruvate(3−) (CHEBI:17271) has functional parent pyruvate (CHEBI:15361)
keto-phenylpyruvate (CHEBI:18005) has functional parent pyruvate (CHEBI:15361)
trans-2-carboxybenzylidenepyruvate(2−) (CHEBI:27040) has functional parent pyruvate (CHEBI:15361)
tetrahydro-4-hydroxyphenylpyruvate (CHEBI:64790) has functional parent pyruvate (CHEBI:15361)
sodium pyruvate (CHEBI:50144) has part pyruvate (CHEBI:15361)
pyruvic acid (CHEBI:32816) is conjugate acid of pyruvate (CHEBI:15361)
IUPAC Name
2-oxopropanoate
Synonyms Sources
2-oxopropanoate ChEBI
2-oxopropanoic acid, ion(1−) ChemIDplus
pyruvate UniProt
Database Links Databases
C00022 KEGG COMPOUND
c0159 UM-BBD
View more database links
Registry Numbers Types Sources
2502 Gmelin Registry Number Gmelin
3587721 Beilstein Registry Number Beilstein
3587721 Reaxys Registry Number Reaxys
57-60-3 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17190852 PubMed citation CiteXplore
21603897 PubMed citation CiteXplore
21823181 PubMed citation CiteXplore
21854850 PubMed citation CiteXplore
22006570 PubMed citation CiteXplore
22016370 PubMed citation CiteXplore
22215378 PubMed citation CiteXplore
22311625 PubMed citation CiteXplore
22451307 PubMed citation CiteXplore
22458763 PubMed citation CiteXplore
Last Modified
14 April 2014

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