Showing metabocard for TG(20:2n6/15:0/22:4(7Z,10Z,13Z,16Z)) (BMDB0106989)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 09:52:13 UTC
Update Date2020-04-22 20:05:00 UTC
BMDB IDBMDB0106989
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(20:2n6/15:0/22:4(7Z,10Z,13Z,16Z))
DescriptionTG(20:2n6/15:0/22:4(7Z,10Z,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(20:2n6/15:0/22:4(7Z,10Z,13Z,16Z)) is made up of one 11Z,14Z-eicosadienoyl(R1), one pentadecanoyl(R2), and one 7Z,10Z,13Z,16Z-docosatetraenoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(11Z,14Z-Eicosadienoyl)-2-pentadecanoyl-3-(7Z,10Z,13Z,16Z-docosatetraenoyl)-glycerolHMDB
1-Eicosadienoyl-2-pentadecanoyl-3-adrenoyl-glycerolHMDB
TAG(20:2/15:0/22:4)HMDB
TAG(20:2n6/15:0/22:4)HMDB
TAG(20:2W6/15:0/22:4)HMDB
TAG(57:6)HMDB
TG(20:2/15:0/22:4)HMDB
TG(20:2n6/15:0/22:4)HMDB
TG(20:2W6/15:0/22:4)HMDB
TG(57:6)HMDB
Tracylglycerol(20:2/15:0/22:4)HMDB
Tracylglycerol(20:2n6/15:0/22:4)HMDB
Tracylglycerol(20:2W6/15:0/22:4)HMDB
Tracylglycerol(57:6)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
TG(20:2n6/15:0/22:4n6)HMDB
TG(20:2W6/15:0/22:4W6)HMDB
Tag(20:2(11Z,14Z)/15:0/22:4(7Z,10Z,13Z,16Z))HMDB
Tag(20:2n6/15:0/22:4n6)HMDB
Tag(20:2W6/15:0/22:4W6)HMDB
Triacylglycerol(20:2(11Z,14Z)/15:0/22:4(7Z,10Z,13Z,16Z))HMDB
Triacylglycerol(20:2/15:0/22:4)HMDB
Triacylglycerol(20:2n6/15:0/22:4n6)HMDB
Triacylglycerol(20:2W6/15:0/22:4W6)HMDB
Triacylglycerol(57:6)HMDB
TG(20:2(11Z,14Z)/15:0/22:4(7Z,10Z,13Z,16Z))HMDB
TG(20:2n6/15:0/22:4(7Z,10Z,13Z,16Z))Lipid Annotator
Chemical FormulaC60H104O6
Average Molecular Weight921.486
Monoisotopic Molecular Weight920.783291069
IUPAC Name(2S)-3-[(11Z,14Z)-icosa-11,14-dienoyloxy]-2-(pentadecanoyloxy)propyl (7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoate
Traditional Name(2S)-3-[(11Z,14Z)-icosa-11,14-dienoyloxy]-2-(pentadecanoyloxy)propyl (7Z,10Z,13Z,16Z)-docosa-7,10,13,16-tetraenoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCC\C=C/C\C=C/CCCCC)(COC(=O)CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCCC
InChI Identifier
InChI=1S/C60H104O6/c1-4-7-10-13-16-19-22-25-27-29-30-32-34-36-39-41-44-47-50-53-59(62)65-56-57(66-60(63)54-51-48-45-42-37-24-21-18-15-12-9-6-3)55-64-58(61)52-49-46-43-40-38-35-33-31-28-26-23-20-17-14-11-8-5-2/h16-17,19-20,25-28,30,32,36,39,57H,4-15,18,21-24,29,31,33-35,37-38,40-56H2,1-3H3/b19-16-,20-17-,27-25-,28-26-,32-30-,39-36-/t57-/m0/s1
InChI KeyNWOLJALSYRNQOS-PKBLFXTLSA-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
logP10.8ALOGPS
logP20.75ChemAxon
logS-8.1ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count53ChemAxon
Refractivity289.4 m³·mol⁻¹ChemAxon
Polarizability120.79 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-0000000009-8b3f72987e1267288f1eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000009-8b3f72987e1267288f1eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01y9-0000049003-596556488af863d1eb08View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-07d3-0059002001-d02a8bc4411cf71142a9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-06sr-0049000000-93ca9f477b82c3d4a106View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0buc-3089000000-35bce584d1275cdadc8cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00fr-8262014179-81b3dd72c230f3ad6087View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-056r-9360000340-aa79e36be23e089d77afView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-004i-1295001300-84ae83b5c36a28f2deb6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0000000009-aaf953b321c442ad75bbView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-0000000009-aaf953b321c442ad75bbView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-0000000009-aaf953b321c442ad75bbView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-0000000009-55a5f4cbcb837dc6b028View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000009-55a5f4cbcb837dc6b028View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-020i-0010049003-b4d0f8ed72e40aff410cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-0000000009-da46f49ffad25d25b336View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-004i-0000000009-da46f49ffad25d25b336View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01b0-0004009004-8fd2020282abd71561f8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-015i-0089044006-84d281228905d6ccab44View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-01ba-0089000000-5317566fc00a62f3cbe7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aor-2049000000-e11e2a585206b700dfbfView in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0053281
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 Compound131763931
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available