Showing metabocard for TG(22:0/20:3n6/22:2(13Z,16Z)) (BMDB0100917)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 00:55:48 UTC
Update Date2020-04-22 19:26:26 UTC
BMDB IDBMDB0100917
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(22:0/20:3n6/22:2(13Z,16Z))
DescriptionTG(22:0/20:3n6/22:2(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(22:0/20:3n6/22:2(13Z,16Z)) is made up of one docosanoyl(R1), one 8Z,11Z,14Z-eicosatrienoyl(R2), and one 13Z,16Z-docosadienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Behenoyl-2-homo-g-linolenoyl-3-docosadienoyl-glycerolHMDB
1-Docosanoyl-2-(8Z,11Z,14Z-eicosatrienoyl)-3-(13Z,16Z-docosadienoyl)-glycerolHMDB
TAG(22:0/20:3/22:2)HMDB
TAG(22:0/20:3n6/22:2)HMDB
TAG(22:0/20:3W6/22:2)HMDB
TAG(64:5)HMDB
TG(22:0/20:3/22:2)HMDB
TG(22:0/20:3n6/22:2)HMDB
TG(22:0/20:3W6/22:2)HMDB
TG(64:5)HMDB
Tracylglycerol(22:0/20:3/22:2)HMDB
Tracylglycerol(22:0/20:3n6/22:2)HMDB
Tracylglycerol(22:0/20:3W6/22:2)HMDB
Tracylglycerol(64:5)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Behenoyl-2-dihomo-gamma-linolenoyl-3-docosadienoyl-glycerolHMDB
TG(22:0/20:3n6/22:2n6)HMDB
TG(22:0/20:3W6/22:2W6)HMDB
Tag(22:0/20:3(8Z,11Z,14Z)/22:2(13Z,16Z))HMDB
Tag(22:0/20:3n6/22:2n6)HMDB
Tag(22:0/20:3W6/22:2W6)HMDB
Triacylglycerol(22:0/20:3(8Z,11Z,14Z)/22:2(13Z,16Z))HMDB
Triacylglycerol(22:0/20:3/22:2)HMDB
Triacylglycerol(22:0/20:3n6/22:2n6)HMDB
Triacylglycerol(22:0/20:3W6/22:2W6)HMDB
Triacylglycerol(64:5)HMDB
TG(22:0/20:3(8Z,11Z,14Z)/22:2(13Z,16Z))HMDB
TG(22:0/20:3n6/22:2(13Z,16Z))Lipid Annotator
Chemical FormulaC67H120O6
Average Molecular Weight1021.691
Monoisotopic Molecular Weight1020.908491584
IUPAC Name(2S)-3-(docosanoyloxy)-2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]propyl (13Z,16Z)-docosa-13,16-dienoate
Traditional Name(2S)-3-(docosanoyloxy)-2-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]propyl (13Z,16Z)-docosa-13,16-dienoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCCCCCCCCCCCCCC)(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/C67H120O6/c1-4-7-10-13-16-19-22-25-28-31-33-36-38-41-44-47-50-53-56-59-65(68)71-62-64(73-67(70)61-58-55-52-49-46-43-40-35-30-27-24-21-18-15-12-9-6-3)63-72-66(69)60-57-54-51-48-45-42-39-37-34-32-29-26-23-20-17-14-11-8-5-2/h16,18-19,21,25,27-28,30,40,43,64H,4-15,17,20,22-24,26,29,31-39,41-42,44-63H2,1-3H3/b19-16-,21-18-,28-25-,30-27-,43-40-/t64-/m1/s1
InChI KeyCPRDOXJZLAUHOY-CTQOOBEISA-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
logP10.82ALOGPS
logP24.23ChemAxon
logS-8.2ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count61ChemAxon
Refractivity320.49 m³·mol⁻¹ChemAxon
Polarizability136.63 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, Positivesplash10-000i-9000000000-2c4bb945bac7c3988d82View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-9000000000-2c4bb945bac7c3988d82View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00s9-3000009400-d913a4967cfb2287c002View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00ri-2019000200-eb0a92cddf779b1327faView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-000i-0019000000-64dc457b53f9883481fcView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-000i-2039000000-10a2e2efb7597dd65375View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-9000000000-7b4e2175fb355434554eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-9000000000-7b4e2175fb355434554eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00s9-3001009400-351a9cd919051f0ac454View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-014r-5009003200-a4f3aad6830d01edb061View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-005i-0009001000-2f3b09d6e154bb1ee075View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-053i-1009000000-eb39f43357a68e2807dbView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-9001001112-59d61d805e8a01ea3ae1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-05gr-9052002155-d2f6debdf57704897760View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000l-1192000140-6b7e1813c46186102e47View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-9000000000-d0b2f6c3de21030a9192View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-004i-9000000000-d0b2f6c3de21030a9192View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00io-9009009900-75511f2fc4d50bb64021View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-9000000000-10e8b9c82c8b5222f4ebView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-9000000000-10e8b9c82c8b5222f4ebView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-9000000000-10e8b9c82c8b5222f4ebView in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0046721
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 Compound131757603
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available