Showing metabocard for TG(24:0/24:1(15Z)/20:3n6) (BMDB0101536)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 01:47:56 UTC
Update Date2020-04-22 19:30:21 UTC
BMDB IDBMDB0101536
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(24:0/24:1(15Z)/20:3n6)
DescriptionTG(24:0/24:1(15Z)/20:3n6) 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(24:0/24:1(15Z)/20:3n6) is made up of one tetracosanoyl(R1), one 15Z-tetracosenoyl(R2), and one 8Z,11Z,14Z-eicosatrienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-Lignoceroyl-2-nervonoyl-3-homo-g-linolenoyl-glycerolHMDB
1-Tetracosanoyl-2-(15Z-tetracosanoyl)-3-(8Z,11Z,14Z-eicosatrienoyl)-glycerolHMDB
TAG(24:0/24:1/20:3)HMDB
TAG(24:0/24:1/20:3n6)HMDB
TAG(24:0/24:1/20:3W6)HMDB
TAG(68:4)HMDB
TG(24:0/24:1/20:3)HMDB
TG(24:0/24:1/20:3n6)HMDB
TG(24:0/24:1/20:3W6)HMDB
TG(68:4)HMDB
Tracylglycerol(24:0/24:1/20:3)HMDB
Tracylglycerol(24:0/24:1/20:3n6)HMDB
Tracylglycerol(24:0/24:1/20:3W6)HMDB
Tracylglycerol(68:4)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Lignoceroyl-2-nervonoyl-3-dihomo-gamma-linolenoyl-glycerolHMDB
TG(24:0/24:1n9/20:3n6)HMDB
TG(24:0/24:1W9/20:3W6)HMDB
Tag(24:0/24:1(15Z)/20:3(8Z,11Z,14Z))HMDB
Tag(24:0/24:1n9/20:3n6)HMDB
Tag(24:0/24:1W9/20:3W6)HMDB
Triacylglycerol(24:0/24:1(15Z)/20:3(8Z,11Z,14Z))HMDB
Triacylglycerol(24:0/24:1/20:3)HMDB
Triacylglycerol(24:0/24:1n9/20:3n6)HMDB
Triacylglycerol(24:0/24:1W9/20:3W6)HMDB
Triacylglycerol(68:4)HMDB
TG(24:0/24:1(15Z)/20:3(8Z,11Z,14Z))HMDB
TG(24:0/24:1(15Z)/20:3n6)Lipid Annotator
Chemical FormulaC71H130O6
Average Molecular Weight1079.815
Monoisotopic Molecular Weight1078.986741906
IUPAC Name(2S)-1-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-3-(tetracosanoyloxy)propan-2-yl (15Z)-tetracos-15-enoate
Traditional Name(2S)-1-[(8Z,11Z,14Z)-icosa-8,11,14-trienoyloxy]-3-(tetracosanoyloxy)propan-2-yl (15Z)-tetracos-15-enoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCCCCCCCCCCCCCCCC)(COC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C71H130O6/c1-4-7-10-13-16-19-22-25-28-31-33-35-37-40-43-46-49-52-55-58-61-64-70(73)76-67-68(66-75-69(72)63-60-57-54-51-48-45-42-39-30-27-24-21-18-15-12-9-6-3)77-71(74)65-62-59-56-53-50-47-44-41-38-36-34-32-29-26-23-20-17-14-11-8-5-2/h18,21,26-27,29-30,42,45,68H,4-17,19-20,22-25,28,31-41,43-44,46-67H2,1-3H3/b21-18-,29-26-,30-27-,45-42-/t68-/m1/s1
InChI KeyFUQSYFKCKNERRH-CQRJRTSZSA-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
logP10.77ALOGPS
logP26.37ChemAxon
logS-8.2ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count66ChemAxon
Refractivity337.78 m³·mol⁻¹ChemAxon
Polarizability145.94 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, Positivesplash10-0002-9000000000-de625ff814881e0aaba7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-de625ff814881e0aaba7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03k9-2000000900-cf13252b077e16639a79View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0ara-1029000200-c293a05dd63c67c13327View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0671-0029000100-cb2d79900ac3fb8de36eView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-066r-2029000000-ccff6df874777cf5ea36View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0udi-0900000000-d7ea502e1bb139d041ebView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0udi-0900000000-d7ea502e1bb139d041ebView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0udi-0900000000-d7ea502e1bb139d041ebView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-9000000000-a291218954a0989b47eeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-9000000000-a291218954a0989b47eeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-02ti-4004000900-9b99ddab29ae1b7e16d4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0ar0-6009400800-aa83a55dbb048753433cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0005-0009200100-7a5b33bf0ff4b31fa008View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aor-1009100000-40e49086b8420a149f32View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0h00-9003000402-01cefe01f2dd2c47b37aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-006t-8019000224-504eea067d46220d66a4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0002-2229200120-91b13dc57e17af159baeView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-9000000000-e7d2925044a0cc421cc5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-e7d2925044a0cc421cc5View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03k9-2001000900-3513224db113fe87730fView in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0047353
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 Compound131758196
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available