CHEBI:16265 - succinic semialdehyde

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name succinic semialdehyde
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:15126, CHEBI:9305, CHEBI:26804
Supplier Information
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Formula C4H6O3
Net Charge 0
Average Mass 102.08864
Monoisotopic Mass 102.03169
InChI InChI=1S/C4H6O3/c5-3-1-2-4(6)7/h3H,1-2H2,(H,6,7)
Metabolite of Species Details
Mus musculus (NCBI:txid10090) Source: BioModels - MODEL1507180067 See: PubMed
Escherichia coli (NCBI:txid562) See: PubMed
Roles Classification
Chemical Role(s): Bronsted acid
A molecular entity capable of donating a hydron to an acceptor (Bronsted base).
(via oxoacid )
Biological Role(s): Escherichia coli metabolite
Any bacterial metabolite produced during a metabolic reaction in Escherichia coli.
mouse metabolite
Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus).
View more via ChEBI Ontology
ChEBI Ontology
Outgoing succinic semialdehyde (CHEBI:16265) has role Escherichia coli metabolite (CHEBI:76971)
succinic semialdehyde (CHEBI:16265) has role mouse metabolite (CHEBI:75771)
succinic semialdehyde (CHEBI:16265) is a aldehydic acid (CHEBI:26643)
succinic semialdehyde (CHEBI:16265) is conjugate acid of 4-oxobutanoate (CHEBI:57706)
Incoming ethyl 4-oxobutanoate (CHEBI:87282) has functional parent succinic semialdehyde (CHEBI:16265)
4-oxobutanoate (CHEBI:57706) is conjugate base of succinic semialdehyde (CHEBI:16265)
4-oxobutanoic acid
Synonyms Sources
3-formylpropanoic acid ChemIDplus
3-formylpropionic acid ChemIDplus
4-Oxobutanoate KEGG COMPOUND
β-formylpropionic acid ChemIDplus
semialdéhyde succinique ChEBI
succinaldehydic acid ChemIDplus
Succinate semialdehyde KEGG COMPOUND
succinic acid semialdehyde ChemIDplus
Succinic semialdehyde KEGG COMPOUND
Manual Xrefs Databases
C00019682 KNApSAcK
c0311 UM-BBD
View more database links
Registry Numbers Types Sources
1745187 Beilstein Registry Number Beilstein
692-29-5 CAS Registry Number ChemIDplus
Last Modified
04 December 2018