Record Information
Version1.0
Creation Date2020-03-25 15:45:01 UTC
Update Date2020-04-22 18:58:12 UTC
BMDB IDBMDB0096449
Secondary Accession NumbersNone
Metabolite Identification
Common NameDG(14:1n5/0:0/14:1n5)
DescriptionDG(14:1n5/0:0/14:1n5) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. It is involved in the phospholipid metabolic pathway.
Structure
Thumb
Synonyms
ValueSource
2-Hydroxy-3-[(5Z)-tetradec-5-enoyloxy]propyl (5Z)-tetradec-5-enoic acidHMDB
Diacylglycerol(28:2)HMDB
DG(14:1/0:0/14:1)HMDB
DAG(14:1N5/0:0/14:1N5)HMDB
DAG(14:1/0:0/14:1)HMDB
Diacylglycerol(14:1W5/0:0/14:1W5)HMDB
Diacylglycerol(14:1n5/0:0/14:1n5)HMDB
DiglycerideHMDB
DAG(14:1W5/0:0/14:1W5)HMDB
DG(14:1W5/0:0/14:1W5)HMDB
1-Myristoleoyl-3-myristoleoyl-sn-glycerolHMDB
DiacylglycerolHMDB
Diacylglycerol(14:1/0:0/14:1)HMDB
DAG(28:2)HMDB
1-(9Z-Tetradecenoyl)-3-(9Z-tetradecenoyl)-sn-glycerolHMDB
DG(28:2)HMDB
DG(14:1n5/0:0/14:1n5)Lipid Annotator
Chemical FormulaC31H56O5
Average Molecular Weight508.784
Monoisotopic Molecular Weight508.412774903
IUPAC Name2-hydroxy-3-[(5Z)-tetradec-5-enoyloxy]propyl (5Z)-tetradec-5-enoate
Traditional Name2-hydroxy-3-[(5Z)-tetradec-5-enoyloxy]propyl (5Z)-tetradec-5-enoate
CAS Registry NumberNot Available
SMILES
[H]C(O)(COC(=O)CCC\C=C/CCCCCCCC)COC(=O)CCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C31H56O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-30(33)35-27-29(32)28-36-31(34)26-24-22-20-18-16-14-12-10-8-6-4-2/h17-20,29,32H,3-16,21-28H2,1-2H3/b19-17-,20-18-
InChI KeyHLHDHRLWUZRJSS-CLFAGFIQSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as 1,3-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 3.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerolipids
Sub ClassDiradylglycerols
Direct Parent1,3-diacylglycerols
Alternative Parents
Substituents
  • 1,3-acyl-sn-glycerol
  • Fatty acid ester
  • Fatty acyl
  • Dicarboxylic acid or derivatives
  • Secondary alcohol
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Alcohol
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Cell membrane
  • Membrane
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP8.77ALOGPS
logP9.5ChemAxon
logS-7.3ALOGPS
pKa (Strongest Acidic)13.63ChemAxon
pKa (Strongest Basic)-3.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area72.83 ŲChemAxon
Rotatable Bond Count28ChemAxon
Refractivity151.53 m³·mol⁻¹ChemAxon
Polarizability64.8 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-0kai-6690300000-f981787f7c93e776515aView in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (1 TMS) - 70eV, Positivesplash10-0q3c-9423020000-21f6d52c1fd947c9be88View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-0290160000-253e9f48e3143fba1bceView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0api-4791200000-18f757b523a4dd4b0a0aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-066r-3941200000-14a9a940e535527edaaeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a6r-0090040000-f7b6b7b472ea686b35cfView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-056r-0090000000-93986669186e018d6ac9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-056r-2290000000-adc2c3e5d9ca87019538View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a4i-1090060000-745333c3b8ff4e4072d1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a59-1090010000-8d340a742595b7952b22View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-004i-1290000000-3c01d4fb0fc25e551094View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-3391470000-26a737a62420a93f9bf2View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0pc0-5594600000-08a026375e0668199cb4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0pej-6493000000-3c1ea6702c97710ef7f6View in MoNA
Biological Properties
Cellular Locations
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0056134
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB098594
KNApSAcK IDNot Available
Chemspider ID74849521
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound131801844
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available