CHEBI:15361 - pyruvate

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
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
Download Molfile XML SDF
Formula C3H3O3
Net Charge -1
Average Mass 87.05412
Monoisotopic Mass 87.00877
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 Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): fundamental metabolite
Any metabolite produced by all living cells.
cofactor
An organic molecule or ion (usually a metal ion) that is required by an enzyme for its activity. It may be attached either loosely (coenzyme) or tightly (prosthetic group).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing pyruvate (CHEBI:15361) has functional parent propionate (CHEBI:17272)
pyruvate (CHEBI:15361) has role cofactor (CHEBI:23357)
pyruvate (CHEBI:15361) has role fundamental metabolite (CHEBI:78675)
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-aminophenyl)pyruvate (CHEBI:143071) 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-bromopyruvate (CHEBI:131592) 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-hydroxyphenylpyruvate (CHEBI:167869) 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
Manual Xrefs 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 Europe PMC
21603897 PubMed citation Europe PMC
21823181 PubMed citation Europe PMC
21854850 PubMed citation Europe PMC
22006570 PubMed citation Europe PMC
22016370 PubMed citation Europe PMC
22215378 PubMed citation Europe PMC
22311625 PubMed citation Europe PMC
22451307 PubMed citation Europe PMC
22458763 PubMed citation Europe PMC
Last Modified
25 July 2019