CHEBI:17290 - (S)-3-hydroxybutyric acid

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (S)-3-hydroxybutyric acid
ChEBI ID CHEBI:17290
ChEBI ASCII Name (S)-3-hydroxybutyric acid
Definition The S-enantiomer of 3-hydroxybutyric acid; a normal human metabolite, that has been found elevated in geriatric patients remitting from depression.
Stars This entity has been manually annotated by the ChEBI Team.
Secondary ChEBI IDs CHEBI:18748, CHEBI:393
Supplier Information
Save molfile Download Molfile
Formula C4H8O3
Net Charge 0
Average Mass 104.10452
Monoisotopic Mass 104.047
InChI InChI=1S/C4H8O3/c1-3(5)2-4(6)7/h3,5H,2H2,1H3,(H,6,7)/t3-/m0/s1
InChIKey WHBMMWSBFZVSSR-VKHMYHEASA-N
SMILES C[C@H](O)CC(O)=O
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): human metabolite
Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
(via 3-hydroxybutyric acid )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (S)-3-hydroxybutyric acid (CHEBI:17290) is a 3-hydroxybutyric acid (CHEBI:20067)
(S)-3-hydroxybutyric acid (CHEBI:17290) is conjugate acid of (S)-3-hydroxybutyrate (CHEBI:11047)
(S)-3-hydroxybutyric acid (CHEBI:17290) is enantiomer of (R)-3-hydroxybutyric acid (CHEBI:17066)
Incoming (S)-3-hydroxybutanoyl-CoA (CHEBI:15453) has functional parent (S)-3-hydroxybutyric acid (CHEBI:17290)
(S)-3-hydroxybutyrate (CHEBI:11047) is conjugate base of (S)-3-hydroxybutyric acid (CHEBI:17290)
(R)-3-hydroxybutyric acid (CHEBI:17066) is enantiomer of (S)-3-hydroxybutyric acid (CHEBI:17290)
IUPAC Name
(3S)-3-hydroxybutanoic acid
Synonyms Sources
(+)-3-hydroxybutyric acid ChEBI
(3S)-3-hydroxybutyric acid ChEBI
(S)-3-hydroxybutanoic acid ChEBI
(S)-3-hydroxybutyric acid ChEBI
(S)-3-Hydroxybutyric acid ChemIDplus
(S)-3HB ChEBI
(S)-β-hydroxybutyric acid ChEBI
L-(+)-3-hydroxybutyric acid ChEBI
L-3-hydroxybutyric acid ChEBI
Database Links Databases
3HL PDBeChem
C03197 KEGG COMPOUND
CPD-1843 MetaCyc
HMDB00758 HMDB
View more database links
Registry Numbers Types Sources
1720567 Reaxys Registry Number Reaxys
1720567 Beilstein Registry Number Beilstein
6168-83-8 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
17048218 PubMed citation Europe PMC
18461320 PubMed citation Europe PMC
19304817 PubMed citation Europe PMC
Last Modified
28 July 2014