Showing metabocard for TG(14:1(9Z)/20:3n6/18:3(6Z,9Z,12Z)) (BMDB0102274)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2020-03-26 03:22:20 UTC
Update Date2020-04-22 19:35:01 UTC
BMDB IDBMDB0102274
Secondary Accession NumbersNone
Metabolite Identification
Common NameTG(14:1(9Z)/20:3n6/18:3(6Z,9Z,12Z))
DescriptionTG(14:1(9Z)/20:3n6/18:3(6Z,9Z,12Z)) 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(14:1(9Z)/20:3n6/18:3(6Z,9Z,12Z)) is made up of one 9Z-tetradecenoyl(R1), one 8Z,11Z,14Z-eicosatrienoyl(R2), and one 6Z,9Z,12Z-octadecatrienoyl(R3).
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-(9Z-Tetradecenoyl)-2-(8Z,11Z,14Z-eicosatrienoyl)-3-(6Z,9Z,12Z-octadecatrienoyl)-glycerolHMDB
1-Myristoleoyl-2-homo-g-linolenoyl-3-g-linolenoyl-glycerolHMDB
TAG(14:1/20:3/18:3)HMDB
TAG(14:1/20:3n6/18:3)HMDB
TAG(14:1/20:3W6/18:3)HMDB
TAG(52:7)HMDB
TG(14:1/20:3/18:3)HMDB
TG(14:1/20:3n6/18:3)HMDB
TG(14:1/20:3W6/18:3)HMDB
TG(52:7)HMDB
Tracylglycerol(14:1/20:3/18:3)HMDB
Tracylglycerol(14:1/20:3n6/18:3)HMDB
Tracylglycerol(14:1/20:3W6/18:3)HMDB
Tracylglycerol(52:7)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1-Myristoleoyl-2-dihomo-gamma-linolenoyl-3-gamma-linolenoyl-glycerolHMDB
TG(14:1n5/20:3n6/18:3n6)HMDB
TG(14:1W5/20:3W6/18:3W6)HMDB
Tag(14:1(9Z)/20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z))HMDB
Tag(14:1n5/20:3n6/18:3n6)HMDB
Tag(14:1W5/20:3W6/18:3W6)HMDB
Triacylglycerol(14:1(9Z)/20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z))HMDB
Triacylglycerol(14:1/20:3/18:3)HMDB
Triacylglycerol(14:1n5/20:3n6/18:3n6)HMDB
Triacylglycerol(14:1W5/20:3W6/18:3W6)HMDB
Triacylglycerol(52:7)HMDB
TG(14:1(9Z)/20:3(8Z,11Z,14Z)/18:3(6Z,9Z,12Z))HMDB
TG(14:1(9Z)/20:3n6/18:3(6Z,9Z,12Z))Lipid Annotator
Chemical FormulaC55H92O6
Average Molecular Weight849.335
Monoisotopic Molecular Weight848.689390682
IUPAC Name(2S)-1-[(6Z,9Z,12Z)-octadeca-6,9,12-trienoyloxy]-3-[(9Z)-tetradec-9-enoyloxy]propan-2-yl (8Z,11Z,14Z)-icosa-8,11,14-trienoate
Traditional Name(2S)-1-[(6Z,9Z,12Z)-octadeca-6,9,12-trienoyloxy]-3-[(9Z)-tetradec-9-enoyloxy]propan-2-yl (8Z,11Z,14Z)-icosa-8,11,14-trienoate
CAS Registry NumberNot Available
SMILES
[H][C@](COC(=O)CCCCCCC\C=C/CCCC)(COC(=O)CCCC\C=C/C\C=C/C\C=C/CCCCC)OC(=O)CCCCCC\C=C/C\C=C/C\C=C/CCCCC
InChI Identifier
InChI=1S/C55H92O6/c1-4-7-10-13-16-19-22-24-26-27-29-31-34-37-40-43-46-49-55(58)61-52(50-59-53(56)47-44-41-38-35-32-21-18-15-12-9-6-3)51-60-54(57)48-45-42-39-36-33-30-28-25-23-20-17-14-11-8-5-2/h15-20,24-26,28-29,31,33,36,52H,4-14,21-23,27,30,32,34-35,37-51H2,1-3H3/b18-15-,19-16-,20-17-,26-24-,28-25-,31-29-,36-33-/t52-/m0/s1
InChI KeyHMTNHQHEYQBSPD-DBWBQWTESA-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
logP10.38ALOGPS
logP18.17ChemAxon
logS-8.2ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count47ChemAxon
Refractivity267.51 m³·mol⁻¹ChemAxon
Polarizability107.91 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, Positivesplash10-014i-0000000090-203838ef8c1943acbce8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-0000000090-203838ef8c1943acbce8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00dl-0000094030-f66efb7b8893bb670e2cView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0a6r-0091010010-a5bc0e3768ceba3fadbcView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-056r-0091000000-60910a06a52cc0f63ccaView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0a6r-2091000000-8ff1ab0f91137c866a55View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00di-0000000090-790bdb2e025b22d14a0aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00di-0000000090-790bdb2e025b22d14a0aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00di-0000000090-790bdb2e025b22d14a0aView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-006t-3130032790-3ebc8e4a000b42d0378bView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-000i-3080010930-841a7e895410310481a9View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000i-2491020120-23497f0192ddef6b3e16View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-0000000090-49e6c97bfc24c76268e8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-0000000090-49e6c97bfc24c76268e8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00dl-0020094030-4a909123c0771fdf6749View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00mk-0094051050-186e3973af2c08f6a8e6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-014i-0069000000-cb1536acc20226e4057dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-0ar0-5089000200-490355660903ae7fe54dView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0a4i-0000000090-c5185c33d02d780ac4cdView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-0000000090-c5185c33d02d780ac4cdView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0a9k-0090099090-46526c5e6405ac34e718View in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
HMDB IDHMDB0048147
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 Compound131758988
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available