Showing metabocard for TG(18:1(9Z)/22:1(13Z)/20:2n6) (BMDB0103885)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 05:44:01 UTC
Update Date2020-04-22 19:45:14 UTC
BMDB IDBMDB0103885
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(18:1(9Z)/22:1(13Z)/20:2n6)
DescriptionTG(18:1(9Z)/22:1(13Z)/20:2n6) 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(18:1(9Z)/22:1(13Z)/20:2n6) is made up of one 9Z-octadecenoyl(R1), one 13Z-docosenoyl(R2), and one 11Z,14Z-eicosadienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(9Z-Octadecenoyl)-2-(13Z-docosenoyl)-3-(11Z,14Z-eicosadienoyl)-glycerolHMDB
1-Oleoyl-2-erucoyl-3-eicosadienoyl-glycerolHMDB
TAG(18:1/22:1/20:2)HMDB
TAG(18:1/22:1/20:2n6)HMDB
TAG(18:1/22:1/20:2W6)HMDB
TAG(60:4)HMDB
TG(18:1/22:1/20:2)HMDB
TG(18:1/22:1/20:2n6)HMDB
TG(18:1/22:1/20:2W6)HMDB
TG(60:4)HMDB
Tracylglycerol(18:1/22:1/20:2)HMDB
Tracylglycerol(18:1/22:1/20:2n6)HMDB
Tracylglycerol(18:1/22:1/20:2W6)HMDB
Tracylglycerol(60:4)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
TG(18:1n9/22:1n9/20:2n6)HMDB
TG(18:1W9/22:1W9/20:2W6)HMDB
Tag(18:1(9Z)/22:1(13Z)/20:2(11Z,14Z))HMDB
Tag(18:1n9/22:1n9/20:2n6)HMDB
Tag(18:1W9/22:1W9/20:2W6)HMDB
Triacylglycerol(18:1(9Z)/22:1(13Z)/20:2(11Z,14Z))HMDB
Triacylglycerol(18:1/22:1/20:2)HMDB
Triacylglycerol(18:1n9/22:1n9/20:2n6)HMDB
Triacylglycerol(18:1W9/22:1W9/20:2W6)HMDB
Triacylglycerol(60:4)HMDB
TG(18:1(9Z)/22:1(13Z)/20:2(11Z,14Z))HMDB
TG(18:1(9Z)/22:1(13Z)/20:2n6)Lipid Annotator
Chemical FormulaC63H114O6
Average Molecular Weight967.599
Monoisotopic Molecular Weight966.861541391
IUPAC Name(2R)-1-[(11Z,14Z)-icosa-11,14-dienoyloxy]-3-[(9Z)-octadec-9-enoyloxy]propan-2-yl (13Z)-docos-13-enoate
Traditional Name(2R)-1-[(11Z,14Z)-icosa-11,14-dienoyloxy]-3-[(9Z)-octadec-9-enoyloxy]propan-2-yl (13Z)-docos-13-enoate
CAS Registry NumberNot Available
SMILES
[H][C@@](COC(=O)CCCCCCCCC\C=C/C\C=C/CCCCC)(COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCCCCCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C63H114O6/c1-4-7-10-13-16-19-22-25-28-30-31-33-36-39-42-45-48-51-54-57-63(66)69-60(58-67-61(64)55-52-49-46-43-40-37-34-27-24-21-18-15-12-9-6-3)59-68-62(65)56-53-50-47-44-41-38-35-32-29-26-23-20-17-14-11-8-5-2/h17,20,25-29,34,60H,4-16,18-19,21-24,30-33,35-59H2,1-3H3/b20-17-,28-25-,29-26-,34-27-/t60-/m0/s1
InChI KeyOSQJHCZDNGROLT-UBCHDMNKSA-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
logP10.78ALOGPS
logP22.81ChemAxon
logS-8.2ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count58ChemAxon
Refractivity300.97 m³·mol⁻¹ChemAxon
Polarizability128.8 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, Positivesplash10-001i-0000000009-e1f534aa3cd28e457504View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-001i-0000000009-e1f534aa3cd28e457504View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0atr-0000009002-aaa1c98888f6f56c195fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-07ci-0095002001-248ad78b1702382c4caeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0bu9-0096001000-288ee38dc5ebfcb42420View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0bu9-3096000000-32308edbdbf8d3161c31View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-066r-0039007007-4919f909ee1b526f1245View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014j-0009000000-53f8e0a6d676d14e1967View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a4r-2019000000-0fe9628987e0728b9f80View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-0000000009-198a1c5ce22246860ed9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000009-198a1c5ce22246860ed9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000i-0000000009-198a1c5ce22246860ed9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-066r-9314005056-57633d25f383296a4997View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-05fr-9107002061-a61bcf3a7bb7272aa50bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-05fu-4619003020-6d3b39fa39546a882ee3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-001i-0000000009-2d69c3e90bff63baf378View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-001i-0000000009-2d69c3e90bff63baf378View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0atr-0010009002-0c6be2ef5cb847fef21eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-0000000009-dfe1b3c3138c126cb711View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-0000000009-dfe1b3c3138c126cb711View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03t0-0040009004-abef1889d110c6eb2e45View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0049968
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 Compound131760730
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available