Showing metabocard for TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) (BMDB0005474)

IdentificationTaxonomyPhysical propertiesSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 23:18:00 UTC
Update Date2020-06-04 20:18:02 UTC
MCDB ID BMDB0005474
Secondary Accession Numbers
  • BMDB05474
Metabolite Identification
Common NameTG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z))
DescriptionTG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)), also known as TG or 1,2,3-tri-(9Z,12Z)-octadecadienoylglycerol, 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. Thus, TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) is considered to be a triradylglycerol lipid molecule. TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) can be biosynthesized from DG(18:2(9Z,12Z)/18:2(9Z,12Z)/0:0) and linoleoyl-CoA through its interaction with the enzyme diacylglycerol O-acyltransferase. In cattle, TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) is involved in the metabolic pathway called de novo triacylglycerol biosynthesis TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z)) pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1,2,3-Propanetriol trilinoleateChEBI
1,2,3-Propenetriol tri(9,12-octadecadienoate)ChEBI
1,2,3-Tri-(9Z,12Z)-octadecadienoylglycerolChEBI
1,2,3-Tri-(9Z,12Z-octadecadienoyl)glycerolChEBI
Glyceryl trilinoleateChEBI
Linoleoyl triglycerideChEBI
TAG(18:2/18:2/18:2)ChEBI
TAG(54:6)ChEBI
TGChEBI
TG(18:2/18:2/18:2)ChEBI
TG(18:2Omega6/18:2omega6/18:2omega6)ChEBI
TG(54:6)ChEBI
Tracylglycerol(18:2omega6/18:2omega6/18:2omega6)ChEBI
Triacylglycerol(18:2/18:2/18:2)ChEBI
Triacylglycerol(54:6)ChEBI
TrilinoleinChEBI
1,2,3-Propanetriol trilinoleic acidGenerator
1,2,3-Propenetriol tri(9,12-octadecadienoic acid)Generator
Glyceryl trilinoleic acidGenerator
Trilinoleic glycerolMeSH
Trilinolein, (all-e)-isomerMeSH
TrilinoelaidateMeSH
Glycerol trilinoleateMeSH
TrilinoelaidinMeSH
TriacylglycerolLipid Annotator, HMDB
1-linoleoyl-2-linoleoyl-3-linoleoyl-glycerolLipid Annotator, HMDB
Tracylglycerol(18:2/18:2/18:2)Lipid Annotator, HMDB
TriglycerideLipid Annotator, HMDB
TG(18:2(9Z,12Z)/18:2(9Z,12Z)/18:2(9Z,12Z))Lipid Annotator
Tracylglycerol(54:6)Lipid Annotator, HMDB
1-(9Z,12Z-octadecadienoyl)-2-(9Z,12Z-octadecadienoyl)-3-(9Z,12Z-octadecadienoyl)-glycerolLipid Annotator, HMDB
TAG(18:2n6/18:2n6/18:2n6)HMDB
TAG(18:2W6/18:2W6/18:2W6)HMDB
TG(18:2n6/18:2n6/18:2n6)HMDB
TG(18:2W6/18:2W6/18:2W6)HMDB
Tracylglycerol(18:2n6/18:2n6/18:2n6)HMDB
Tracylglycerol(18:2W6/18:2W6/18:2W6)HMDB
Chemical FormulaC57H98O6
Average Molecular Weight879.3844
Monoisotopic Molecular Weight878.736340868
IUPAC Name1,3-bis[(9Z,12Z)-octadeca-9,12-dienoyloxy]propan-2-yl (9Z,12Z)-octadeca-9,12-dienoate
Traditional Nametriglyceride
CAS Registry Number537-40-6
SMILES
[H]C(COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)(COC(=O)CCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCCC\C=C/C\C=C/CCCCC
InChI Identifier
InChI=1S/C57H98O6/c1-4-7-10-13-16-19-22-25-28-31-34-37-40-43-46-49-55(58)61-52-54(63-57(60)51-48-45-42-39-36-33-30-27-24-21-18-15-12-9-6-3)53-62-56(59)50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h16-21,25-30,54H,4-15,22-24,31-53H2,1-3H3/b19-16-,20-17-,21-18-,28-25-,29-26-,30-27-
InChI KeyHBOQXIRUPVQLKX-BBWANDEASA-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
  • Octadecanoid
  • 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 Descriptors
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP10.65ALOGPS
logP19.42ChemAxon
logS-8ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count50ChemAxon
Refractivity275.6 m³·mol⁻¹ChemAxon
Polarizability113.22 ųChemAxon
Number of Rings0ChemAxon
Bioavailability0ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectrum TypeDescriptionSplash KeyDeposition DateView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-0000000090-457c6a39735c24cfc3892017-10-04View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-0000000090-457c6a39735c24cfc3892017-10-04View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-002b-0000090070-ef777a07709237ac99092017-10-04View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, NegativeNot Available2020-06-30View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, NegativeNot Available2020-06-30View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, NegativeNot Available2020-06-30View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-0000000090-5099cbb5f7bc6957ba4b2021-09-22View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000090-5099cbb5f7bc6957ba4b2021-09-22View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0f79-0090009090-3e4373abb45a87b03e802021-09-22View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-004i-0085093080-c7bc55e449fa12690f152021-09-23View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-066r-0019010000-81ae524e633327a05c2d2021-09-23View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0ar0-2069022000-d0a4e7925cdfe33aed972021-09-23View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0udi-0000000009-cfe884cde7363d5f41ad2021-09-23View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0udi-0000000009-cfe884cde7363d5f41ad2021-09-23View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0udi-0000000009-cfe884cde7363d5f41ad2021-09-23View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-0000000090-b1fb8423285a4927f1c62021-09-24View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-0000000090-b1fb8423285a4927f1c62021-09-24View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-002b-0010090070-d30e70ba14e1cf2d439f2021-09-24View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-002b-1130060690-768316edee989f13c3512021-09-25View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03di-5190020420-c5f1decec11501e92a692021-09-25View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03di-0190010000-b9029b9a77af129586452021-09-25View Spectrum
Concentrations
StatusValueReferenceDetails
Detected and Quantified7.5 +/- 0.3 uM details
Detected and Quantified20 +/- 1 uM details
Detected and Quantified89 +/- 4 uM details
Detected and Quantified0.26 +/- 0.02 uM details
HMDB IDHMDB0005474
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB094336
KNApSAcK IDNot Available
Chemspider ID4479674
KEGG Compound IDC00422
BioCyc IDTriacylglycerols
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound5322095
PDB IDNot Available
ChEBI ID75844
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Tang C, Zhang K, Zhan T, Zhao Q, Zhang J: Metabolic Characterization of Dairy Cows Treated with Gossypol by Blood Biochemistry and Body Fluid Untargeted Metabolome Analyses. J Agric Food Chem. 2017 Oct 25;65(42):9369-9378. doi: 10.1021/acs.jafc.7b03544. Epub 2017 Oct 17. [PubMed:28965405 ]
  2. A. Foroutan et al. (2019). A. Foroutan et al. The Chemical Composition of Commercial Cow's Milk (in preparation). Journal of Agricultural and Food Chemistry.