Showing metabocard for TG(15:0/20:2n6/18:3(9Z,12Z,15Z)) (BMDB0098214)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-25 18:11:12 UTC
Update Date2020-04-22 19:09:21 UTC
BMDB IDBMDB0098214
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(15:0/20:2n6/18:3(9Z,12Z,15Z))
DescriptionTG(15:0/20:2n6/18:3(9Z,12Z,15Z)) 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(15:0/20:2n6/18:3(9Z,12Z,15Z)) is made up of one pentadecanoyl(R1), one 11Z,14Z-eicosadienoyl(R2), and one 9Z,12Z,15Z-octadecatrienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Pentadecanoyl-2-(11Z,14Z-eicosadienoyl)-3-(9Z,12Z,15Z-octadeatrienoyl)-glycerolHMDB
1-Pentadecanoyl-2-eicosadienoyl-3-a-linolenoyl-glycerolHMDB
TAG(15:0/20:2/18:3)HMDB
TAG(15:0/20:2n6/18:3)HMDB
TAG(15:0/20:2W6/18:3)HMDB
TAG(53:5)HMDB
TG(15:0/20:2/18:3)HMDB
TG(15:0/20:2n6/18:3)HMDB
TG(15:0/20:2W6/18:3)HMDB
TG(53:5)HMDB
Tracylglycerol(15:0/20:2/18:3)HMDB
Tracylglycerol(15:0/20:2n6/18:3)HMDB
Tracylglycerol(15:0/20:2W6/18:3)HMDB
Tracylglycerol(53:5)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Pentadecanoyl-2-eicosadienoyl-3-alpha-linolenoyl-glycerolHMDB
TG(15:0/20:2n6/18:3n3)HMDB
TG(15:0/20:2W6/18:3W3)HMDB
Tag(15:0/20:2(11Z,14Z)/18:3(9Z,12Z,15Z))HMDB
Tag(15:0/20:2n6/18:3n3)HMDB
Tag(15:0/20:2W6/18:3W3)HMDB
Triacylglycerol(15:0/20:2(11Z,14Z)/18:3(9Z,12Z,15Z))HMDB
Triacylglycerol(15:0/20:2/18:3)HMDB
Triacylglycerol(15:0/20:2n6/18:3n3)HMDB
Triacylglycerol(15:0/20:2W6/18:3W3)HMDB
Triacylglycerol(53:5)HMDB
TG(15:0/20:2(11Z,14Z)/18:3(9Z,12Z,15Z))HMDB
TG(15:0/20:2n6/18:3(9Z,12Z,15Z))Lipid Annotator
Chemical FormulaC56H98O6
Average Molecular Weight867.394
Monoisotopic Molecular Weight866.736340876
IUPAC Name(2S)-1-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]-3-(pentadecanoyloxy)propan-2-yl (11Z,14Z)-icosa-11,14-dienoate
Traditional Name(2S)-1-[(9Z,12Z,15Z)-octadeca-9,12,15-trienoyloxy]-3-(pentadecanoyloxy)propan-2-yl (11Z,14Z)-icosa-11,14-dienoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCCCCCCC)(COC(=O)CCCCCCC\C=C/C\C=C/C\C=C/CC)OC(=O)CCCCCCCCC\C=C/C\C=C/CCCCC
InChI Identifier
InChI=1S/C56H98O6/c1-4-7-10-13-16-19-22-25-27-28-30-32-35-38-41-44-47-50-56(59)62-53(51-60-54(57)48-45-42-39-36-33-24-21-18-15-12-9-6-3)52-61-55(58)49-46-43-40-37-34-31-29-26-23-20-17-14-11-8-5-2/h8,11,16-17,19-20,25-27,29,53H,4-7,9-10,12-15,18,21-24,28,30-52H2,1-3H3/b11-8-,19-16-,20-17-,27-25-,29-26-/t53-/m0/s1
InChI KeyPYAPRJGPZHLBDL-GCNIVINMSA-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
logP10.73ALOGPS
logP19.34ChemAxon
logS-8.1ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count50ChemAxon
Refractivity269.88 m³·mol⁻¹ChemAxon
Polarizability113.39 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-0000000090-98b694cfbb034b59da0dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-001i-0000000090-98b694cfbb034b59da0dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0atr-0000094030-b1304c6582a63f4c0882View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a6u-0091010010-85261c45077a48289c19View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-05dl-0091000000-3f6c58906cb19db77955View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a6u-2091000000-2feae8a36ce67c84808eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-0000000090-dda8476a14cf922d334aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-0000000090-dda8476a14cf922d334aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03t0-0090099090-e593624725fe0ce50e0dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-001i-0000000090-2fc52b0093aad42a0824View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-001i-0000000090-2fc52b0093aad42a0824View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-05r9-0020094030-a3c404e2f1e2272d574bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0159-0093051050-2f841de648691a7e7f7eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-00li-0069000000-a842e32937e7027bda8aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0ar0-3096000000-b66c2525b5a286ac2fc1View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-0000000090-2c11b4097d268e0fc4f3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000090-2c11b4097d268e0fc4f3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000i-0000000090-2c11b4097d268e0fc4f3View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-4040041690-dba3211094022b5d9c35View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-5090000320-596f04299e7b8911c547View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-2391000000-6f1d510a49767528236aView in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0043475
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 Compound131754595
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available