CHEBI:131434 - 5-hydroxyhexanoic acid

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ChEBI Name 5-hydroxyhexanoic acid
ChEBI ID CHEBI:131434
Definition A medium-chain fatty acid that is hexanoic acid substituted at position 5 by a hydroxy group.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C6H12O3
Net Charge 0
Average Mass 132.158
Monoisotopic Mass 132.07864
InChI InChI=1S/C6H12O3/c1-5(7)3-2-4-6(8)9/h5,7H,2-4H2,1H3,(H,8,9)
InChIKey YDCRNMJQROAWFT-UHFFFAOYSA-N
SMILES OC(CCCC(=O)O)C
Metabolite of Species Details
Homo sapiens (NCBI:txid9606) See: PubMed
Homo sapiens (NCBI:txid9606) See: MetaboLights Study
Homo sapiens (NCBI:txid9606) 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): human urinary metabolite
Any metabolite (endogenous or exogenous) found in human urine samples.
View more via ChEBI Ontology
ChEBI Ontology
Outgoing 5-hydroxyhexanoic acid (CHEBI:131434) has functional parent hexanoic acid (CHEBI:30776)
5-hydroxyhexanoic acid (CHEBI:131434) has role human urinary metabolite (CHEBI:84087)
5-hydroxyhexanoic acid (CHEBI:131434) is a (ω−1)-hydroxy fatty acid (CHEBI:78954)
5-hydroxyhexanoic acid (CHEBI:131434) is a medium-chain fatty acid (CHEBI:59554)
5-hydroxyhexanoic acid (CHEBI:131434) is conjugate acid of 5-hydroxyhexanoate (CHEBI:132985)
Incoming 5-hydroxyhexanoate (CHEBI:132985) is conjugate base of 5-hydroxyhexanoic acid (CHEBI:131434)
IUPAC Name
5-hydroxyhexanoic acid
Synonyms Sources
5-hydroxy caproic acid LIPID MAPS
5-hydroxy-hexanoic acid LIPID MAPS
5-hydroxycaproic acid ChEBI
5-OH-caproic acid HMDB
Manual Xrefs Databases
149280 ChemSpider
HMDB0000525 HMDB
LMFA01050014 LIPID MAPS
View more database links
Registry Numbers Types Sources
1749065 Reaxys Registry Number Reaxys
44843-89-2 CAS Registry Number ChemIDplus
Citations Waiting for Citations Types Sources
575058 PubMed citation Europe PMC
640132 PubMed citation Europe PMC
6897376 PubMed citation Europe PMC
Last Modified
14 November 2016