Showing metabocard for TG(20:3n6/15:0/22:2(13Z,16Z)) (BMDB0107375)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 10:21:45 UTC
Update Date2020-04-22 20:07:26 UTC
BMDB IDBMDB0107375
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(20:3n6/15:0/22:2(13Z,16Z))
DescriptionTG(20:3n6/15:0/22:2(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(20:3n6/15:0/22:2(13Z,16Z)) is made up of one 8Z,11Z,14Z-eicosatrienoyl(R1), one pentadecanoyl(R2), and one 13Z,16Z-docosadienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(8Z,11Z,14Z-Eicosatrienoyl)-2-pentadecanoyl-3-(13Z,16Z-docosadienoyl)-glycerolHMDB
1-Homo-g-linolenoyl-2-pentadecanoyl-3-docosadienoyl-glycerolHMDB
TAG(20:3/15:0/22:2)HMDB
TAG(20:3n6/15:0/22:2)HMDB
TAG(20:3W6/15:0/22:2)HMDB
TAG(57:5)HMDB
TG(20:3/15:0/22:2)HMDB
TG(20:3n6/15:0/22:2)HMDB
TG(20:3W6/15:0/22:2)HMDB
TG(57:5)HMDB
Tracylglycerol(20:3/15:0/22:2)HMDB
Tracylglycerol(20:3n6/15:0/22:2)HMDB
Tracylglycerol(20:3W6/15:0/22:2)HMDB
Tracylglycerol(57:5)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Dihomo-gamma-linolenoyl-2-pentadecanoyl-3-docosadienoyl-glycerolHMDB
TG(20:3n6/15:0/22:2n6)HMDB
TG(20:3W6/15:0/22:2W6)HMDB
Tag(20:3(8Z,11Z,14Z)/15:0/22:2(13Z,16Z))HMDB
Tag(20:3n6/15:0/22:2n6)HMDB
Tag(20:3W6/15:0/22:2W6)HMDB
Triacylglycerol(20:3(8Z,11Z,14Z)/15:0/22:2(13Z,16Z))HMDB
Triacylglycerol(20:3/15:0/22:2)HMDB
Triacylglycerol(20:3n6/15:0/22:2n6)HMDB
Triacylglycerol(20:3W6/15:0/22:2W6)HMDB
Triacylglycerol(57:5)HMDB
TG(20:3(8Z,11Z,14Z)/15:0/22:2(13Z,16Z))HMDB
TG(20:3n6/15:0/22:2(13Z,16Z))Lipid Annotator
Chemical FormulaC60H106O6
Average Molecular Weight923.502
Monoisotopic Molecular Weight922.798941133
IUPAC Name(2R)-3-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-2-(pentadecanoyloxy)propyl (13Z,16Z)-docosa-13,16-dienoate
Traditional Name(2R)-3-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-2-(pentadecanoyloxy)propyl (13Z,16Z)-docosa-13,16-dienoate
CAS Registry NumberNot Available
SMILES
[H][C@@](COC(=O)CCCCCCCCCCC\C=C/C\C=C/CCCCC)(COC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCCC
InChI Identifier
InChI=1S/C60H106O6/c1-4-7-10-13-16-19-22-25-27-29-30-32-34-36-39-41-44-47-50-53-59(62)65-56-57(66-60(63)54-51-48-45-42-37-24-21-18-15-12-9-6-3)55-64-58(61)52-49-46-43-40-38-35-33-31-28-26-23-20-17-14-11-8-5-2/h16-17,19-20,25-28,33,35,57H,4-15,18,21-24,29-32,34,36-56H2,1-3H3/b19-16-,20-17-,27-25-,28-26-,35-33-/t57-/m0/s1
InChI KeySEFKRPOMLSLDGU-RDOMJWQOSA-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
logP21.12ChemAxon
logS-8.2ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count54ChemAxon
Refractivity288.28 m³·mol⁻¹ChemAxon
Polarizability121.48 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0000000009-26540c836d64d4149cf0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-0000000009-26540c836d64d4149cf0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01d9-0000049003-cc8261ab96c40d700ab2View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-052r-0059002001-e8b1e58cae7646254e3fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-052r-0049000000-95c31018e0c993e488caView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-052u-3089000000-de27be5dca64ff8b879dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-0000000009-a939d5ac479081e6195eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-004i-0000000009-a939d5ac479081e6195eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03io-0009099009-493fb90442613c5d3c75View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00dr-0089027006-23f1a21361ea8db5024aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-016s-0089000000-80da7ddf0651959e4efeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aor-3059000000-2de7427a57339578731dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0000000009-c4c50a82b77cf08f38c4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-0000000009-c4c50a82b77cf08f38c4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01ci-0010049003-76f7f2e998eb0674cc17View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-0000000009-a08b75a7835242c2fcbfView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-0000000009-a08b75a7835242c2fcbfView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0002-0000000009-a08b75a7835242c2fcbfView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-05ir-9420013225-c11e63fedb28ed75aca2View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-05dj-9141001531-74fefb57fea986596bf4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-004j-3493001400-d52c36b41609ab93d3efView in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0053667
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 Compound131764307
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available