Showing metabocard for TG(24:1(15Z)/20:3n6/24:1(15Z)) (BMDB0105989)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 08:37:15 UTC
Update Date2020-04-22 19:58:39 UTC
BMDB IDBMDB0105989
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(24:1(15Z)/20:3n6/24:1(15Z))
DescriptionTG(24:1(15Z)/20:3n6/24:1(15Z)) belongs to the family of triradyglycerols, which are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. Their general formula is [R1]OCC(CO[R2])O[R3]. TG(24:1(15Z)/20:3n6/24:1(15Z)) is made up of one 15Z-tetracosenoyl(R1), one 8Z,11Z,14Z-eicosatrienoyl(R2), and one 15Z-tetracosenoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Nervonoyl-2-dihomo-gamma-linolenoyl-3-nervonoyl-glycerolHMDB
TG(24:1/20:3/24:1)HMDB
TG(24:1n9/20:3n6/24:1n9)HMDB
TG(24:1W9/20:3W6/24:1W9)HMDB
TG(68:5)HMDB
Tag(24:1(15Z)/20:3(8Z,11Z,14Z)/24:1(15Z))HMDB
Tag(24:1/20:3/24:1)HMDB
Tag(24:1n9/20:3n6/24:1n9)HMDB
Tag(24:1W9/20:3W6/24:1W9)HMDB
Tag(68:5)HMDB
Triacylglycerol(24:1(15Z)/20:3(8Z,11Z,14Z)/24:1(15Z))HMDB
Triacylglycerol(24:1/20:3/24:1)HMDB
Triacylglycerol(24:1n9/20:3n6/24:1n9)HMDB
Triacylglycerol(24:1W9/20:3W6/24:1W9)HMDB
Triacylglycerol(68:5)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
TG(24:1(15Z)/20:3(8Z,11Z,14Z)/24:1(15Z))HMDB
Tracylglycerol(24:1/20:3W6/24:1)HMDB
TG(24:1/20:3W6/24:1)HMDB
TAG(24:1/20:3W6/24:1)HMDB
Tracylglycerol(24:1/20:3/24:1)HMDB
TG(24:1/20:3n6/24:1)HMDB
1-Nervonoyl-2-homo-g-linolenoyl-3-nervonoyl-glycerolHMDB
Tracylglycerol(24:1/20:3n6/24:1)HMDB
TAG(24:1/20:3n6/24:1)HMDB
1-(15Z-Tetracosanoyl)-2-(8Z,11Z,14Z-eicosatrienoyl)-3-(15Z-tetracosanoyl)-glycerolHMDB
Tracylglycerol(68:5)HMDB
TG(24:1(15Z)/20:3n6/24:1(15Z))Lipid Annotator
Chemical FormulaC71H128O6
Average Molecular Weight1077.7724
Monoisotopic Molecular Weight1076.971091828
IUPAC Name2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-3-[(15Z)-tetracos-15-enoyloxy]propyl (15Z)-tetracos-15-enoate
Traditional Name2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-3-[(15Z)-tetracos-15-enoyloxy]propyl (15Z)-tetracos-15-enoate
CAS Registry NumberNot Available
SMILES
[H]C(COC(=O)CCCCCCCCCCCCC\C=C/CCCCCCCC)(COC(=O)CCCCCCCCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC
InChI Identifier
InChI=1S/C71H128O6/c1-4-7-10-13-16-19-22-25-28-31-33-35-37-40-42-45-48-51-54-57-60-63-69(72)75-66-68(77-71(74)65-62-59-56-53-50-47-44-39-30-27-24-21-18-15-12-9-6-3)67-76-70(73)64-61-58-55-52-49-46-43-41-38-36-34-32-29-26-23-20-17-14-11-8-5-2/h18,21,25-30,44,47,68H,4-17,19-20,22-24,31-43,45-46,48-67H2,1-3H3/b21-18-,28-25-,29-26-,30-27-,47-44-
InChI KeyRXAVSLVLSNEBOO-JLMRWRGNSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as triacylglycerols. These are glycerides consisting of three fatty acid chains covalently bonded to a glycerol molecule through ester linkages.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerolipids
Sub ClassTriradylcglycerols
Direct ParentTriacylglycerols
Alternative Parents
Substituents
  • Triacyl-sn-glycerol
  • Tricarboxylic acid or derivatives
  • Fatty acid ester
  • Fatty acyl
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Carbonyl group
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Adiposome
  • 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
logP10.76ALOGPS
logP26.01ChemAxon
logS-8.3ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count65ChemAxon
Refractivity338.89 m³·mol⁻¹ChemAxon
Polarizability144.95 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, PositiveNot AvailableView in JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-9000000000-b8329c752ecd5ef1779aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-b8329c752ecd5ef1779aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03t9-3000000900-b28db81851f450f70268View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-9000000000-4f8ba55ac34af3ece627View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-4f8ba55ac34af3ece627View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0002-9000000000-4f8ba55ac34af3ece627View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-9000000000-1a1a333f9cb8cd1d94e3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-1a1a333f9cb8cd1d94e3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03t9-3000000900-26d82eec8511b44f9589View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-05r0-7009101600-ca9ef3e3552b89459e32View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0pca-0019501100-9095fcc55397adc53363View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aor-2009300000-a1c6d1e6a0bae2c48ca5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-9211000303-a7ecc518b139a1e72328View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-059i-8152100419-1ad464e232e391c3fcaaView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000m-2397000252-3a41d234d0e10249231cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-001i-9000000000-dc8245f8cdcb1d1ec76bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-001i-9000000000-dc8245f8cdcb1d1ec76bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01o0-4004000900-8b16831ed920a1fec386View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0052205
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound131762896
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available