Showing metabocard for TG(20:2n6/15:0/22:5(4Z,7Z,10Z,13Z,16Z)) (BMDB0106990)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 09:52:18 UTC
Update Date2020-04-22 20:05:00 UTC
BMDB IDBMDB0106990
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(20:2n6/15:0/22:5(4Z,7Z,10Z,13Z,16Z))
DescriptionTG(20:2n6/15:0/22:5(4Z,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(20:2n6/15:0/22:5(4Z,7Z,10Z,13Z,16Z)) is made up of one 11Z,14Z-eicosadienoyl(R1), one pentadecanoyl(R2), and one 4Z,7Z,10Z,13Z,16Z-docosapentaenoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(11Z,14Z-Eicosadienoyl)-2-pentadecanoyl-3-(4Z,7Z,10Z,13Z,16Z-docosapentaenoyl)-glycerolHMDB
1-Eicosadienoyl-2-pentadecanoyl-3-osbondoyl-glycerolHMDB
TAG(20:2/15:0/22:5)HMDB
TAG(20:2n6/15:0/22:5)HMDB
TAG(20:2W6/15:0/22:5)HMDB
TAG(57:7)HMDB
TG(20:2/15:0/22:5)HMDB
TG(20:2n6/15:0/22:5)HMDB
TG(20:2W6/15:0/22:5)HMDB
TG(57:7)HMDB
Tracylglycerol(20:2/15:0/22:5)HMDB
Tracylglycerol(20:2n6/15:0/22:5)HMDB
Tracylglycerol(20:2W6/15:0/22:5)HMDB
Tracylglycerol(57:7)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
TG(20:2n6/15:0/22:5n6)HMDB
TG(20:2W6/15:0/22:5W6)HMDB
Tag(20:2(11Z,14Z)/15:0/22:5(4Z,7Z,10Z,13Z,16Z))HMDB
Tag(20:2n6/15:0/22:5n6)HMDB
Tag(20:2W6/15:0/22:5W6)HMDB
Triacylglycerol(20:2(11Z,14Z)/15:0/22:5(4Z,7Z,10Z,13Z,16Z))HMDB
Triacylglycerol(20:2/15:0/22:5)HMDB
Triacylglycerol(20:2n6/15:0/22:5n6)HMDB
Triacylglycerol(20:2W6/15:0/22:5W6)HMDB
Triacylglycerol(57:7)HMDB
TG(20:2(11Z,14Z)/15:0/22:5(4Z,7Z,10Z,13Z,16Z))HMDB
TG(20:2n6/15:0/22:5(4Z,7Z,10Z,13Z,16Z))Lipid Annotator
Chemical FormulaC60H102O6
Average Molecular Weight919.47
Monoisotopic Molecular Weight918.767641004
IUPAC Name(2S)-3-[(11Z,14Z)-icosa-11,14-dienoyloxy]-2-(pentadecanoyloxy)propyl (4Z,7Z,10Z,13Z,16Z)-docosa-4,7,10,13,16-pentaenoate
Traditional Name(2S)-3-[(11Z,14Z)-icosa-11,14-dienoyloxy]-2-(pentadecanoyloxy)propyl (4Z,7Z,10Z,13Z,16Z)-docosa-4,7,10,13,16-pentaenoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCC\C=C/C\C=C/CCCCC)(COC(=O)CC\C=C/C\C=C/C\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCCC
InChI Identifier
InChI=1S/C60H102O6/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/h16-17,19-20,25-28,30,32,36,39,44,47,57H,4-15,18,21-24,29,31,33-35,37-38,40-43,45-46,48-56H2,1-3H3/b19-16-,20-17-,27-25-,28-26-,32-30-,39-36-,47-44-/t57-/m0/s1
InChI KeyMDKUGPDJBZYZJR-CAPAOAOGSA-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
logP10.74ALOGPS
logP20.39ChemAxon
logS-8.1ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count52ChemAxon
Refractivity290.52 m³·mol⁻¹ChemAxon
Polarizability118.59 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, Positivesplash10-000i-0000000009-045ec6f8407f3f08ff01View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000009-045ec6f8407f3f08ff01View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-02br-0000049003-fea64e53d0676bbab084View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-06vu-0059002001-3b8ebb55d661ca8d59e5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0bvr-0049000000-58dcf5d314e9f6b2c04cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0bvu-3079000000-3973ef59b594a3d1fdecView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-0000000009-851cc31f741315fbeae5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-0000000009-851cc31f741315fbeae5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-042r-0010049003-d41cab866eb57a4d29f7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-0000000009-9f1f7e554ca9e734d3f4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-004i-0000000009-9f1f7e554ca9e734d3f4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01b0-0004009004-eaa82ea83b28f0b497b0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-06a0-0089033004-f6b9c03097fb40d28ed9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014i-0089000000-93daa41ff501a11d8968View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aor-2059000000-af967e088d32c6a69270View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-016r-4151024169-9a1b46e60a10a5b6af35View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-056r-9241000240-80305d76060eabe3901eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-004i-1196001310-60e14a69ae14cc9c1a32View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0000000009-7ce04c573ea95ce3baa4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0006-0000000009-7ce04c573ea95ce3baa4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0006-0000000009-7ce04c573ea95ce3baa4View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0053282
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 Compound131763932
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available