Showing metabocard for TG(24:1(15Z)/20:3n6/22:2(13Z,16Z)) (BMDB0105995)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 08:37:42 UTC
Update Date2020-04-22 19:58:41 UTC
BMDB IDBMDB0105995
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(24:1(15Z)/20:3n6/22:2(13Z,16Z))
DescriptionTG(24:1(15Z)/20:3n6/22:2(13Z,16Z)) 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)/20:3n6/22:2(13Z,16Z)) is made up of one 15Z-tetracosenoyl(R1), one 8Z,11Z,14Z-eicosatrienoyl(R2), and one 13Z,16Z-docosadienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(15Z-Tetracosanoyl)-2-(8Z,11Z,14Z-eicosatrienoyl)-3-(13Z,16Z-docosadienoyl)-glycerolHMDB
1-Nervonoyl-2-homo-g-linolenoyl-3-docosadienoyl-glycerolHMDB
TAG(24:1/20:3/22:2)HMDB
TAG(24:1/20:3n6/22:2)HMDB
TAG(24:1/20:3W6/22:2)HMDB
TAG(66:6)HMDB
TG(24:1/20:3/22:2)HMDB
TG(24:1/20:3n6/22:2)HMDB
TG(24:1/20:3W6/22:2)HMDB
TG(66:6)HMDB
Tracylglycerol(24:1/20:3/22:2)HMDB
Tracylglycerol(24:1/20:3n6/22:2)HMDB
Tracylglycerol(24:1/20:3W6/22:2)HMDB
Tracylglycerol(66:6)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Nervonoyl-2-dihomo-gamma-linolenoyl-3-docosadienoyl-glycerolHMDB
TG(24:1n9/20:3n6/22:2n6)HMDB
TG(24:1W9/20:3W6/22:2W6)HMDB
Tag(24:1(15Z)/20:3(8Z,11Z,14Z)/22:2(13Z,16Z))HMDB
Tag(24:1n9/20:3n6/22:2n6)HMDB
Tag(24:1W9/20:3W6/22:2W6)HMDB
Triacylglycerol(24:1(15Z)/20:3(8Z,11Z,14Z)/22:2(13Z,16Z))HMDB
Triacylglycerol(24:1/20:3/22:2)HMDB
Triacylglycerol(24:1n9/20:3n6/22:2n6)HMDB
Triacylglycerol(24:1W9/20:3W6/22:2W6)HMDB
Triacylglycerol(66:6)HMDB
TG(24:1(15Z)/20:3(8Z,11Z,14Z)/22:2(13Z,16Z))HMDB
TG(24:1(15Z)/20:3n6/22:2(13Z,16Z))Lipid Annotator
Chemical FormulaC69H122O6
Average Molecular Weight1047.729
Monoisotopic Molecular Weight1046.924141648
IUPAC Name(2S)-3-[(13Z,16Z)-docosa-13,16-dienoyloxy]-2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]propyl (15Z)-tetracos-15-enoate
Traditional Name(2S)-3-[(13Z,16Z)-docosa-13,16-dienoyloxy]-2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]propyl (15Z)-tetracos-15-enoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCCCCCC\C=C/CCCCCCCC)(COC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC
InChI Identifier
InChI=1S/C69H122O6/c1-4-7-10-13-16-19-22-25-28-31-33-34-36-39-41-44-47-50-53-56-59-62-68(71)74-65-66(75-69(72)63-60-57-54-51-48-45-42-37-30-27-24-21-18-15-12-9-6-3)64-73-67(70)61-58-55-52-49-46-43-40-38-35-32-29-26-23-20-17-14-11-8-5-2/h17-18,20-21,25-30,42,45,66H,4-16,19,22-24,31-41,43-44,46-65H2,1-3H3/b20-17-,21-18-,28-25-,29-26-,30-27-,45-42-/t66-/m1/s1
InChI KeyACMWFFAEUVQODP-PGLMRKETSA-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
logP10.86ALOGPS
logP24.75ChemAxon
logS-8.3ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count62ChemAxon
Refractivity330.81 m³·mol⁻¹ChemAxon
Polarizability139.21 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, Positivesplash10-03di-9000000000-f834c99065c0990b2852View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03di-9000000000-f834c99065c0990b2852View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03ed-3000004900-5833c5d6640c41274eb6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014s-1009000100-77c901e1a7f1d4f02a2fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014r-0009000000-2cc107f0800ff70e0bc9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0670-2029000000-401ac6a1e1b96bfeba30View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-9000000000-7bef74e0dad9bf6e1043View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-9000000000-7bef74e0dad9bf6e1043View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-014i-9000000000-7bef74e0dad9bf6e1043View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-9200001103-1fe5cf3d95df8cf59b4fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0abi-9052001136-e5de0dd5bc6768d92ed1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-052n-1464000290-bc5969561ff4a5b89871View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0udi-9000000000-8a64132a34501016bd36View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0udi-9000000000-8a64132a34501016bd36View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0ue8-9009009900-ae30dbb50c4ece0f433bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-03di-9000000000-31a3241080d402c294cdView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03di-9000000000-31a3241080d402c294cdView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03ed-3001004900-9c09a7cc1001b714b953View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0002-6009102300-8371722d280948e254a6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a7r-0009200000-1c0065d72f5fd52f028dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4i-2009100000-308123080b2a5ad21b68View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0052211
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 CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available