Showing metabocard for TG(20:3n6/15:0/20:4(5Z,8Z,11Z,14Z)) (BMDB0107374)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 10:21:40 UTC
Update Date2020-04-22 20:07:26 UTC
BMDB IDBMDB0107374
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(20:3n6/15:0/20:4(5Z,8Z,11Z,14Z))
DescriptionTG(20:3n6/15:0/20:4(5Z,8Z,11Z,14Z)) 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(20:3n6/15:0/20:4(5Z,8Z,11Z,14Z)) is made up of one 8Z,11Z,14Z-eicosatrienoyl(R1), one pentadecanoyl(R2), and one 5Z,8Z,11Z,14Z-eicosatetraenoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(8Z,11Z,14Z-Eicosatrienoyl)-2-pentadecanoyl-3-(5Z,8Z,11Z,14Z-eicosatetraenoyl)-glycerolHMDB
1-Homo-g-linolenoyl-2-pentadecanoyl-3-arachidonoyl-glycerolHMDB
TAG(20:3/15:0/20:4)HMDB
TAG(20:3n6/15:0/20:4)HMDB
TAG(20:3W6/15:0/20:4)HMDB
TAG(55:7)HMDB
TG(20:3/15:0/20:4)HMDB
TG(20:3n6/15:0/20:4)HMDB
TG(20:3W6/15:0/20:4)HMDB
TG(55:7)HMDB
Tracylglycerol(20:3/15:0/20:4)HMDB
Tracylglycerol(20:3n6/15:0/20:4)HMDB
Tracylglycerol(20:3W6/15:0/20:4)HMDB
Tracylglycerol(55:7)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Dihomo-gamma-linolenoyl-2-pentadecanoyl-3-arachidonoyl-glycerolHMDB
TG(20:3n6/15:0/20:4n6)HMDB
TG(20:3W6/15:0/20:4W6)HMDB
Tag(20:3(8Z,11Z,14Z)/15:0/20:4(5Z,8Z,11Z,14Z))HMDB
Tag(20:3n6/15:0/20:4n6)HMDB
Tag(20:3W6/15:0/20:4W6)HMDB
Triacylglycerol(20:3(8Z,11Z,14Z)/15:0/20:4(5Z,8Z,11Z,14Z))HMDB
Triacylglycerol(20:3/15:0/20:4)HMDB
Triacylglycerol(20:3n6/15:0/20:4n6)HMDB
Triacylglycerol(20:3W6/15:0/20:4W6)HMDB
Triacylglycerol(55:7)HMDB
TG(20:3(8Z,11Z,14Z)/15:0/20:4(5Z,8Z,11Z,14Z))HMDB
TG(20:3n6/15:0/20:4(5Z,8Z,11Z,14Z))Lipid Annotator
Chemical FormulaC58H98O6
Average Molecular Weight891.416
Monoisotopic Molecular Weight890.736340876
IUPAC Name(2S)-3-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-2-(pentadecanoyloxy)propyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate
Traditional Name(2S)-3-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-2-(pentadecanoyloxy)propyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC)(COC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCCC
InChI Identifier
InChI=1S/C58H98O6/c1-4-7-10-13-16-19-22-25-27-29-31-33-36-38-41-44-47-50-56(59)62-53-55(64-58(61)52-49-46-43-40-35-24-21-18-15-12-9-6-3)54-63-57(60)51-48-45-42-39-37-34-32-30-28-26-23-20-17-14-11-8-5-2/h16-17,19-20,25-28,31-34,38,41,55H,4-15,18,21-24,29-30,35-37,39-40,42-54H2,1-3H3/b19-16-,20-17-,27-25-,28-26-,33-31-,34-32-,41-38-/t55-/m1/s1
InChI KeyMEYKWGDKIXEKDC-UYYNSSENSA-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
logP10.64ALOGPS
logP19.5ChemAxon
logS-8.1ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count50ChemAxon
Refractivity281.31 m³·mol⁻¹ChemAxon
Polarizability114.34 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, Positivesplash10-0a4i-0000000009-197a5dc5ba8d2b793fc9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-0000000009-197a5dc5ba8d2b793fc9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000j-0000094030-4d3aa7c19a63c205cfd7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-052r-0095004030-3227d6ef879eb22df9ceView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0a4r-0079001000-371f3686c55e1478119bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0pbl-3197000000-15ab31fddf7454f32930View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-001i-0095062030-d4db36a721f80e88a6f3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014j-0089010000-671535b601baf6c1e841View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aos-1059000000-fc46e86b2d5cd413415fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-03di-0000000009-d6da12e4f6ac764387ffView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-03di-0000000009-d6da12e4f6ac764387ffView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03di-0000000009-d6da12e4f6ac764387ffView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-002f-3131021390-1ce5e110e3a44b75a431View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-056r-8291000740-73b23e57af9e3e9dd75dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-004i-0192000100-9c59a83bf980cb4d253aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-0000000090-6759ab099210b1992f1eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-0000000090-6759ab099210b1992f1eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0xr8-0009099090-0a8223b0a6ac2ed94d62View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-0000000009-adeeb76f17ca8bffdf93View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-0000000009-adeeb76f17ca8bffdf93View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000i-0020094030-c10d15ed59388a2263a3View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0053666
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 Compound131764306
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available