(S)-2-hydroxybutyric acid (CHEBI:50613)

ChEBI > Main

Main

ChEBI Ontology

Automatic Xrefs

Reactions

Pathways

Models

ChEBI Name	(S)-2-hydroxybutyric acid

ChEBI ID	CHEBI:50613

ChEBI ASCII Name	(S)-2-hydroxybutyric acid

Definition	An optically active form of 2-hydroxybutyric acid having (S)-configuration.

Stars	This entity has been manually annotated by the ChEBI Team.

Supplier Information

Download	Molfile XML SDF

Formula

C4H8O3

Net Charge

Average Mass

104.10452

Monoisotopic Mass

104.04734

InChI

InChI=1S/C4H8O3/c1-2-3(5)4(6)7/h3,5H,2H2,1H3,(H,6,7)/t3-/m0/s1

InChIKey

AFENDNXGAFYKQO-VKHMYHEASA-N

SMILES

CC[C@H](O)C(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 2-hydroxybutyric acid ) algal metabolite Any eukaryotic metabolite produced during a metabolic reaction in algae including unicellular organisms like chlorella and diatoms to multicellular organisms like giant kelps and brown algae. (via 2-hydroxybutyric acid )

ChEBI Ontology
Outgoing	(S)-2-hydroxybutyric acid (CHEBI:50613) is a (2S)-2-hydroxy monocarboxylic acid (CHEBI:17375) (S)-2-hydroxybutyric acid (CHEBI:50613) is a 2-hydroxybutyric acid (CHEBI:1148) (S)-2-hydroxybutyric acid (CHEBI:50613) is conjugate acid of (S)-2-hydroxybutyrate (CHEBI:73709) (S)-2-hydroxybutyric acid (CHEBI:50613) is enantiomer of (R)-2-hydroxybutyric acid (CHEBI:50612)

Incoming	(S)-2-hydroxybutyrate (CHEBI:73709) is conjugate base of (S)-2-hydroxybutyric acid (CHEBI:50613) (R)-2-hydroxybutyric acid (CHEBI:50612) is enantiomer of (S)-2-hydroxybutyric acid (CHEBI:50613)

IUPAC Name

(2S)-2-hydroxybutanoic acid

Registry Number	Type	Source
1720940	Reaxys Registry Number	Reaxys

Last Modified

04 May 2018