CHEBI:37374 - (S)-3-hydroxytetradecanoic acid

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ChEBI Name (S)-3-hydroxytetradecanoic acid
ChEBI ID CHEBI:37374
ChEBI ASCII Name (S)-3-hydroxytetradecanoic acid
Definition A C14, long-chain hydroxy fatty acid and enantiomer of the biologically active (R)-3-hydroxytetradecanoic acid.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C14H28O3
Net Charge 0
Average Mass 244.37030
Monoisotopic Mass 244.20384
InChI InChI=1S/C14H28O3/c1-2-3-4-5-6-7-8-9-10-11-13(15)12-14(16)17/h13,15H,2-12H2,1H3,(H,16,17)/t13-/m0/s1
InChIKey ATRNZOYKSNPPBF-ZDUSSCGKSA-N
SMILES CCCCCCCCCCC[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 )
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ChEBI Ontology
Outgoing (S)-3-hydroxytetradecanoic acid (CHEBI:37374) has functional parent tetradecanoic acid (CHEBI:28875)
(S)-3-hydroxytetradecanoic acid (CHEBI:37374) is a 3-hydroxy monocarboxylic acid (CHEBI:35969)
(S)-3-hydroxytetradecanoic acid (CHEBI:37374) is a hydroxy fatty acid (CHEBI:24654)
(S)-3-hydroxytetradecanoic acid (CHEBI:37374) is conjugate acid of (S)-3-hydroxytetradecanoate (CHEBI:138437)
(S)-3-hydroxytetradecanoic acid (CHEBI:37374) is enantiomer of (R)-3-hydroxytetradecanoic acid (CHEBI:42539)
Incoming (S)-3-hydroxytetradecanoyl-CoA (CHEBI:27466) has functional parent (S)-3-hydroxytetradecanoic acid (CHEBI:37374)
(S)-3-hydroxytetradecanoate (CHEBI:138437) is conjugate base of (S)-3-hydroxytetradecanoic acid (CHEBI:37374)
(R)-3-hydroxytetradecanoic acid (CHEBI:42539) is enantiomer of (S)-3-hydroxytetradecanoic acid (CHEBI:37374)
IUPAC Name
(3S)-3-hydroxytetradecanoic acid
Synonyms Sources
(S)-3-hydroxymyristic acid ChEBI
3S-hydroxy-tetradecanoic acid ChEBI
C14:0 3(S)-OH ChEBI
C14:0 3-OH
Note: (2015-03-26) Ambiguous as stereochemistry is not specified.
 ChEBI
L-β-hydroxymyristic acid ChemIDplus
Manual Xref Database
LMFA01050323 LIPID MAPS
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Registry Numbers Types Sources
35683-15-9 CAS Registry Number ChemIDplus
4667647 Beilstein Registry Number Beilstein
Last Modified
20 September 2017