CHEBI:17071 - glycolaldehyde

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ChEBI Name glycolaldehyde
ChEBI ID CHEBI:17071
Definition The glycolaldehyde derived from ethylene glycol. The parent of the class of glycolaldehydes.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:5474, CHEBI:14347, CHEBI:24386
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Formula C2H4O2
Net Charge 0
Average Mass 60.052
Monoisotopic Mass 60.02113
InChI InChI=1S/C2H4O2/c3-1-2-4/h1,4H,2H2
InChIKey WGCNASOHLSPBMP-UHFFFAOYSA-N
SMILES [H]C(=O)CO
Metabolite of Species Details
Saccharomyces cerevisiae (NCBI:txid4932) Source: yeast.sf.net See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Homo sapiens (NCBI:txid9606) See: DOI
Roles Classification
Biological Role(s): fundamental metabolite
Any metabolite produced by all living cells.
human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
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ChEBI Ontology
Outgoing glycolaldehyde (CHEBI:17071) has role fundamental metabolite (CHEBI:78675)
glycolaldehyde (CHEBI:17071) has role human metabolite (CHEBI:77746)
glycolaldehyde (CHEBI:17071) is a glycolaldehydes (CHEBI:24387)
glycolaldehyde (CHEBI:17071) is tautomer of (Z)-1,2-ethenediol (CHEBI:131198)
Incoming glycolaldehyde phosphate (CHEBI:136456) has functional parent glycolaldehyde (CHEBI:17071)
glycolaldehyde triphosphate (CHEBI:137677) has functional parent glycolaldehyde (CHEBI:17071)
(Z)-1,2-ethenediol (CHEBI:131198) is tautomer of glycolaldehyde (CHEBI:17071)
IUPAC Name
hydroxyacetaldehyde
Synonyms Sources
GLYCOALDEHYDE ChemIDplus
Glycolaldehyde KEGG COMPOUND
glycolaldehyde UniProt
Glycolic aldehyde ChemIDplus
glycollaldehyde NIST Chemistry WebBook
Hydroxyacetaldehyde KEGG COMPOUND
Methylol formaldehyde ChemIDplus
Monomethylolformaldehyde ChemIDplus
Manual Xrefs Databases
C00007457 KNApSAcK
C00266 KEGG COMPOUND
DW3 PDBeChem
ECMDB02165 ECMDB
FDB030893 FooDB
Glycolaldehyde Wikipedia
GLYCOLALDEHYDE MetaCyc
HMDB0003344 HMDB
YMDB00343 YMDB
View more database links
Registry Numbers Types Sources
141-46-8 CAS Registry Number KEGG COMPOUND
141-46-8 CAS Registry Number NIST Chemistry WebBook
141-46-8 CAS Registry Number ChemIDplus
506029 Reaxys Registry Number Reaxys
506029 Beilstein Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
20960220 PubMed citation Europe PMC
21378371 PubMed citation Europe PMC
21472960 PubMed citation Europe PMC
21820089 PubMed citation Europe PMC
23543734 PubMed citation Europe PMC
29400466 PubMed citation Europe PMC
35348319 PubMed citation Europe PMC
35624799 PubMed citation Europe PMC
Last Modified
06 June 2022