Showing metabocard for TG(16:0/18:1(9Z)/18:1(9Z))[iso3] (BMDB0005382)

IdentificationTaxonomyPhysical propertiesSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 23:16:08 UTC
Update Date2020-06-04 20:34:16 UTC
MCDB ID BMDB0005382
Secondary Accession Numbers
  • BMDB05382
Metabolite Identification
Common NameTG(16:0/18:1(9Z)/18:1(9Z))[iso3]
DescriptionTG(16:0/18:1(9Z)/18:1(9Z))[iso3], also known as tag(16:0/18:1/18:1) or glycerol dioleate palmitate, 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. TG(16:0/18:1(9Z)/18:1(9Z))[iso3] is possibly soluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). TG(16:0/18:1(9Z)/18:1(9Z))[iso3] can be biosynthesized from DG(16:0/18:1(9Z)/0:0) and oleoyl-CoA; which is mediated by the enzyme diacylglycerol O-acyltransferase. In cattle, TG(16:0/18:1(9Z)/18:1(9Z))[iso3] is involved in the metabolic pathway called de novo triacylglycerol biosynthesis TG(16:0/18:1(9Z)/18:1(9Z)) pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1,2-Di-(9Z)-octadecenoyl-3-hexadecanoylglycerolChEBI
1-Hexadecanoyl-2,3-di-(9Z)-octadecenoylglycerolChEBI
Glycerol dioleate palmitateChEBI
PalmitodioleinChEBI
Palmitoyl-dioleylglycerolChEBI
TAG(16:0/18:1/18:1)ChEBI
TAG(52:2)ChEBI
TG(16:0/18:1/18:1)ChEBI
TG(16:0/18:1omega9/18:1omega9)ChEBI
TG(52:2)ChEBI
Triacylglycerol(16:0/18:1/18:1)ChEBI
Triacylglycerol(16:0/18:1omega9/18:1omega9)ChEBI
Triacylglycerol(52:2)ChEBI
Triglyceride OOPChEBI
Triglyceride pooChEBI
Glycerol dioleic acid palmitic acidGenerator
1,2-DO-3PGMeSH
1-Palmitoyl-2-oleoyl-3-oleoyl-glycerolHMDB
TAG(16:0/18:1n9/18:1n9)HMDB
TAG(16:0/18:1W9/18:1W9)HMDB
TG(16:0/18:1n9/18:1n9)HMDB
TG(16:0/18:1W9/18:1W9)HMDB
Tracylglycerol(16:0/18:1/18:1)HMDB
Tracylglycerol(16:0/18:1n9/18:1n9)HMDB
Tracylglycerol(16:0/18:1W9/18:1W9)HMDB
Tracylglycerol(52:2)HMDB
TriacylglycerolHMDB
TriglycerideHMDB
1,2-Dioleoyl-3-palmitoylglycerolMeSH
Chemical FormulaC55H102O6
Average Molecular Weight859.3948
Monoisotopic Molecular Weight858.767640996
IUPAC Name1-(hexadecanoyloxy)-3-[(9Z)-octadec-9-enoyloxy]propan-2-yl (9Z)-octadec-9-enoate
Traditional Name1-(hexadecanoyloxy)-3-[(9Z)-octadec-9-enoyloxy]propan-2-yl (9Z)-octadec-9-enoate
CAS Registry Number27071-84-7
SMILES
CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCC\C=C/CCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C55H102O6/c1-4-7-10-13-16-19-22-25-27-30-33-36-39-42-45-48-54(57)60-51-52(50-59-53(56)47-44-41-38-35-32-29-24-21-18-15-12-9-6-3)61-55(58)49-46-43-40-37-34-31-28-26-23-20-17-14-11-8-5-2/h25-28,52H,4-24,29-51H2,1-3H3/b27-25-,28-26-
InChI KeyJFISYPWOVQNHLS-LBXGSASVSA-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 Descriptors
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP10.74ALOGPS
logP19.98ChemAxon
logS-8ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count52ChemAxon
Refractivity261.93 m³·mol⁻¹ChemAxon
Polarizability114.61 ųChemAxon
Number of Rings0ChemAxon
Bioavailability0ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectrum TypeDescriptionSplash KeyDeposition DateView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0arc-0091062040-7e06467f2719b88e86ef2016-08-01View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-00kr-0093021210-3ba7069c466418e557702016-08-01View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-01w0-0091004610-61f0fee473558520d5712016-08-01View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0bu9-0090020010-e3bc77682e7741eb0dd32016-08-03View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-06sr-0090000000-afbaada0b835b3c9afef2016-08-03View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-06sr-1090000000-385a5601c5b287bcc1402016-08-03View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-014i-0000000090-d19de471e852da520bd52021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-0000000090-d19de471e852da520bd52021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-04k0-0090040040-68e5502e6b49f8fdd88f2021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-004i-0000000090-737f74f071afb11b73a82021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-004i-0000000090-737f74f071afb11b73a82021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0kdi-0030099070-239560399f08435bbd082021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-001i-0000000090-8124134fd02fc15952b32021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-001i-0000000090-8124134fd02fc15952b32021-10-21View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-001i-0000000090-8124134fd02fc15952b32021-10-21View Spectrum
Concentrations
StatusValueReferenceDetails
Detected and Quantified668 +/- 6 uM details
Detected and Quantified1072 +/- 59 uM details
Detected and Quantified3094 +/- 208 uM details
Detected and Quantified26 +/- 4 uM details
HMDB IDHMDB0303020
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB007308
KNApSAcK IDNot Available
Chemspider ID13628595
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound25240174
PDB IDNot Available
ChEBI ID75848
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Tang C, Zhang K, Zhan T, Zhao Q, Zhang J: Metabolic Characterization of Dairy Cows Treated with Gossypol by Blood Biochemistry and Body Fluid Untargeted Metabolome Analyses. J Agric Food Chem. 2017 Oct 25;65(42):9369-9378. doi: 10.1021/acs.jafc.7b03544. Epub 2017 Oct 17. [PubMed:28965405 ]
  2. A. Foroutan et al. (2019). A. Foroutan et al. The Chemical Composition of Commercial Cow's Milk (in preparation). Journal of Agricultural and Food Chemistry.