Showing metabocard for 3-Oxodecanoic acid (BMDB0010724)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesenzymes (1) Show 1 proteinXML
Record Information
Version1.0
Creation Date2016-10-03 18:12:34 UTC
Update Date2020-05-21 16:27:15 UTC
BMDB IDBMDB0010724
Secondary Accession Numbers
  • BMDB10724
Metabolite Identification
Common Name3-Oxodecanoic acid
Description3-Oxodecanoic acid, also known as 3-oxodecanoic acid or 3-oxodecanoic acid, belongs to the class of organic compounds known as medium-chain keto acids and derivatives. These are keto acids with a 6 to 12 carbon atoms long side chain. 3-Oxodecanoic acid is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. 3-Oxodecanoic acid exists in all eukaryotes, ranging from yeast to humans. 3-Oxodecanoic acid participates in a number of enzymatic reactions, within cattle. In particular, 3-Oxodecanoic acid can be biosynthesized from caprylic acid and malonic acid; which is catalyzed by the enzyme fatty acid synthase. Beta ketoacyl synthase domain. In addition, 3-Oxodecanoic acid can be converted into (R)-3-hydroxydecanoic acid; which is mediated by the enzyme fatty acid synthase. Beta ketoacyl synthase domain. In cattle, 3-oxodecanoic acid is involved in the metabolic pathway called fatty acid biosynthesis pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
3-OxodecanoateGenerator
3-Ketodecanoic acidHMDB
3-Oxocapric acidHMDB
beta-Ketocapric acidHMDB
beta-Ketodecanoic acidHMDB
beta-Oxodecanoic acidHMDB
3-KetodecanoateHMDB
3-OxocaprateHMDB
b-KetocaprateHMDB
b-Ketocapric acidHMDB
beta-KetocaprateHMDB
Β-ketocaprateHMDB
Β-ketocapric acidHMDB
b-KetodecanoateHMDB
b-Ketodecanoic acidHMDB
beta-KetodecanoateHMDB
Β-ketodecanoateHMDB
Β-ketodecanoic acidHMDB
b-OxodecanoateHMDB
b-Oxodecanoic acidHMDB
beta-OxodecanoateHMDB
Β-oxodecanoateHMDB
Β-oxodecanoic acidHMDB
Chemical FormulaC10H18O3
Average Molecular Weight186.2481
Monoisotopic Molecular Weight186.125594442
IUPAC Name3-oxodecanoic acid
Traditional Name3-oxodecanoic acid
CAS Registry NumberNot Available
SMILES
CCCCCCCC(=O)CC(O)=O
InChI Identifier
InChI=1S/C10H18O3/c1-2-3-4-5-6-7-9(11)8-10(12)13/h2-8H2,1H3,(H,12,13)
InChI KeyYXTHWTPUTHTODU-UHFFFAOYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as medium-chain keto acids and derivatives. These are keto acids with a 6 to 12 carbon atoms long side chain.
KingdomOrganic compounds
Super ClassOrganic acids and derivatives
ClassKeto acids and derivatives
Sub ClassMedium-chain keto acids and derivatives
Direct ParentMedium-chain keto acids and derivatives
Alternative Parents
Substituents
  • Medium-chain keto acid
  • Beta-keto acid
  • 1,3-dicarbonyl compound
  • Beta-hydroxy ketone
  • Ketone
  • Monocarboxylic acid or derivatives
  • Carboxylic acid
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External Descriptors
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Membrane
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP2.61ALOGPS
logP2.92ChemAxon
logS-2.7ALOGPS
pKa (Strongest Acidic)4.44ChemAxon
pKa (Strongest Basic)-7.5ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area54.37 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity50.17 m³·mol⁻¹ChemAxon
Polarizability21.19 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Biological Properties
Cellular Locations
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0010724
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB027872
KNApSAcK IDNot Available
Chemspider ID4446109
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound5282982
PDB IDNot Available
ChEBI ID37157
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Enzymes

Enzyme Details
1. Fatty acid synthase
General function:
Secondary metabolites biosynthesis, transport and catabolism
Specific function:
Fatty acid synthetase catalyzes the formation of long-chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH. This multifunctional protein has 7 catalytic activities as an acyl carrier protein.
Gene Name:
FASN
Uniprot ID:
Q71SP7
Molecular weight:
274554.0
Reactions
Caprylic acid + Malonic acid → 3-Oxodecanoic aciddetails
3-Oxodecanoic acid → (R)-3-Hydroxydecanoic aciddetails