Showing metabocard for TG(24:1(15Z)/24:0/20:2n6) (BMDB0105800)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 08:22:53 UTC
Update Date2020-04-22 19:57:22 UTC
BMDB IDBMDB0105800
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(24:1(15Z)/24:0/20:2n6)
DescriptionTG(24:1(15Z)/24:0/20:2n6) 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(24:1(15Z)/24:0/20:2n6) is made up of one 15Z-tetracosenoyl(R1), one tetracosanoyl(R2), and one 11Z,14Z-eicosadienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(15Z-Tetracosanoyl)-2-tetracosanoyl-3-(11Z,14Z-eicosadienoyl)-glycerolHMDB
1-Nervonoyl-2-lignoceroyl-3-eicosadienoyl-glycerolHMDB
TAG(24:1/24:0/20:2)HMDB
TAG(24:1/24:0/20:2n6)HMDB
TAG(24:1/24:0/20:2W6)HMDB
TAG(68:3)HMDB
TG(24:1/24:0/20:2)HMDB
TG(24:1/24:0/20:2n6)HMDB
TG(24:1/24:0/20:2W6)HMDB
TG(68:3)HMDB
Tracylglycerol(24:1/24:0/20:2)HMDB
Tracylglycerol(24:1/24:0/20:2n6)HMDB
Tracylglycerol(24:1/24:0/20:2W6)HMDB
Tracylglycerol(68:3)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
TG(24:1n9/24:0/20:2n6)HMDB
TG(24:1W9/24:0/20:2W6)HMDB
Tag(24:1(15Z)/24:0/20:2(11Z,14Z))HMDB
Tag(24:1n9/24:0/20:2n6)HMDB
Tag(24:1W9/24:0/20:2W6)HMDB
Triacylglycerol(24:1(15Z)/24:0/20:2(11Z,14Z))HMDB
Triacylglycerol(24:1/24:0/20:2)HMDB
Triacylglycerol(24:1n9/24:0/20:2n6)HMDB
Triacylglycerol(24:1W9/24:0/20:2W6)HMDB
Triacylglycerol(68:3)HMDB
TG(24:1(15Z)/24:0/20:2(11Z,14Z))HMDB
TG(24:1(15Z)/24:0/20:2n6)Lipid Annotator
Chemical FormulaC71H132O6
Average Molecular Weight1081.831
Monoisotopic Molecular Weight1081.00239197
IUPAC Name(2S)-3-[(11Z,14Z)-icosa-11,14-dienoyloxy]-2-(tetracosanoyloxy)propyl (15Z)-tetracos-15-enoate
Traditional Name(2S)-3-[(11Z,14Z)-icosa-11,14-dienoyloxy]-2-(tetracosanoyloxy)propyl (15Z)-tetracos-15-enoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCCCCCCCC\C=C/CCCCCCCC)(COC(=O)CCCCCCCCC\C=C/C\C=C/CCCCC)OC(=O)CCCCCCCCCCCCCCCCCCCCCCC
InChI Identifier
InChI=1S/C71H132O6/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/h18,21,25,27-28,30,68H,4-17,19-20,22-24,26,29,31-67H2,1-3H3/b21-18-,28-25-,30-27-/t68-/m1/s1
InChI KeyJWWYPJRNYQLXQX-KLPDHWSGSA-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
logP10.68ALOGPS
logP26.73ChemAxon
logS-8.2ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count67ChemAxon
Refractivity336.66 m³·mol⁻¹ChemAxon
Polarizability147.53 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-de9a0fe766ab316bdae4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-de9a0fe766ab316bdae4View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-04w9-2000000900-6f5e28f2aca636e48f30View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0ara-1029000200-d80f221956bab5ed3d5aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0ap1-0029000100-a405332bcc4262840110View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-066r-2029000000-86dd68e1922b8d4c5b6cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-02di-6009200600-a0beb90bce6c7dd8b845View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0005-0009200100-faca3eab354e41341075View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0aov-1009000000-7257750e61e893676bd6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-000i-9000000000-018d7eba0436922e216dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-9000000000-018d7eba0436922e216dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01bi-4004000900-1a5a62630d8bd10e8bdaView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-001i-9211000401-b00196dbd671080bfa2fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-106s-9116000332-05a7b4336148099b333cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0udl-2419100110-1d8dd89c03ba626b19e2View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0udi-0900000000-867b71750668e19b6c7cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0udi-0900000000-867b71750668e19b6c7cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0udi-0900000000-867b71750668e19b6c7cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-9000000000-6bfe4993df27caf1bb7fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-9000000000-6bfe4993df27caf1bb7fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-04w9-2001000900-e0c684353ba88bdd5b47View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0052016
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 Compound131762708
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available