Showing metabocard for TG(16:0/16:0/18:1(9Z))[iso3] (BMDB0005360)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2016-09-30 23:15:43 UTC
Update Date2020-04-22 15:15:27 UTC
BMDB IDBMDB0005360
Secondary Accession Numbers
  • BMDB05360
Metabolite Identification
Common NameTG(16:0/16:0/18:1(9Z))[iso3]
DescriptionTG(16:0/16:0/18:1(9Z))[iso3] 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. Thus, TG(16:0/16:0/18:1(9Z))[iso3] is considered to be a triradylglycerol lipid molecule. TG(16:0/16:0/18:1(9Z))[iso3] is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. TG(16:0/16:0/18:1(9Z))[iso3] can be biosynthesized from DG(16:0/16:0/0:0) and oleoyl-CoA through its interaction with the enzyme diacylglycerol O-acyltransferase. In cattle, TG(16:0/16:0/18:1(9Z))[iso3] is involved in the metabolic pathway called de novo triacylglycerol biosynthesis TG(16:0/16:0/18:1(9Z)) pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
1-oleoyl-2-palmitoyl-3-palmitoyl-glycerol SMPDB
TG(18:1/16:0/16:0) SMPDB
TG(18:1n9/16:0/16:0) SMPDB
TG(18:1w9/16:0/16:0) SMPDB
TG(50:1) SMPDB, HMDB
Tag(18:1(9Z)/16:0/16:0) SMPDB
Tag(18:1/16:0/16:0) SMPDB
Tag(18:1n9/16:0/16:0) SMPDB
Tag(18:1w9/16:0/16:0) SMPDB
Tag(50:1) SMPDB, HMDB
Triacylglycerol(18:1(9Z)/16:0/16:0) SMPDB
Triacylglycerol(18:1/16:0/16:0) SMPDB
Triacylglycerol(18:1n9/16:0/16:0) SMPDB
Triacylglycerol(18:1w9/16:0/16:0) SMPDB
Triacylglycerol(50:1) SMPDB
Triacylglycerol SMPDB, HMDB
TriglycerideSMPDB, HMDB
TG(18:1(9Z)/16:0/16:0)SMPDB
1-Palmitoyl-2-palmitoyl-3-oleoyl-glycerolHMDB
TAG(16:0/16:0/18:1)HMDB
TAG(16:0/16:0/18:1n9)HMDB
TAG(16:0/16:0/18:1W9)HMDB
TG(16:0/16:0/18:1)HMDB
TG(16:0/16:0/18:1n9)HMDB
TG(16:0/16:0/18:1W9)HMDB
Tracylglycerol(16:0/16:0/18:1)HMDB
Tracylglycerol(16:0/16:0/18:1n9)HMDB
Tracylglycerol(16:0/16:0/18:1W9)HMDB
Tracylglycerol(50:1)HMDB
Chemical FormulaC53H100O6
Average Molecular Weight833.3575
Monoisotopic Molecular Weight832.751990932
IUPAC Name(2R)-2,3-bis(hexadecanoyloxy)propyl (9Z)-octadec-9-enoate
Traditional Nametriglyceride
CAS Registry NumberNot Available
SMILES
[H]\C(CCCCCCCC)=C(/[H])CCCCCCCC(=O)OC[C@@]([H])(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC
InChI Identifier
InChI=1S/C53H100O6/c1-4-7-10-13-16-19-22-25-26-29-31-34-37-40-43-46-52(55)58-49-50(59-53(56)47-44-41-38-35-32-28-24-21-18-15-12-9-6-3)48-57-51(54)45-42-39-36-33-30-27-23-20-17-14-11-8-5-2/h25-26,50H,4-24,27-49H2,1-3H3/b26-25-/t50-/m1/s1
InChI KeyYHMDGPZOSGBQRH-YYSBDVFPSA-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
Ontology
StatusDetected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • Adiposome
  • Cell membrane
  • Membrane
Physical Properties
StateSolid
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Predicted Properties
PropertyValueSource
logP10.68ALOGPS
logP19.45ChemAxon
logS-7.9ALOGPS
pKa (Strongest Basic)-6.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count0ChemAxon
Polar Surface Area78.9 ŲChemAxon
Rotatable Bond Count51ChemAxon
Refractivity251.61 m³·mol⁻¹ChemAxon
Polarizability111.49 ųChemAxon
Number of Rings0ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectra
Spectrum TypeDescriptionSplash Key
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 21V, positivesplash10-001i-0000000090-299b19287571b2af17ffView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 24V, positivesplash10-001i-0000000090-928944a718d4657aa18eView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 34V, positivesplash10-001i-0000050090-60aee82e21212e85b8abView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 38V, positivesplash10-003r-0000090080-a433ca058d496bd01afaView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 49V, positivesplash10-0fb9-0010090010-11a196fbbdd487c271dbView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 54V, positivesplash10-0fb9-0010090000-8474f27907c5240137deView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 74V, positivesplash10-0fc1-9532070000-5d1e3e10909877b7d9a1View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 83V, positivesplash10-000t-9521020000-39ab0b87062dc9299a5fView in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 99V, positivesplash10-000t-9400000000-4e0ddd9058669beb2476View in MoNA
LC-MS/MSLC-MS/MS Spectrum - Orbitrap 109V, positivesplash10-000t-9300000000-38d6f17b5e6b30d9e1f9View in MoNA
LC-MS/MSLC-MS/MS Spectrum - n/a 58V, positivesplash10-0fb9-0000090000-f24e58b2cd4b315d3e8fView in MoNA
Biological Properties
Cellular Locations
  • Adiposome
  • Cell membrane
  • Membrane
Biospecimen Locations
  • Milk
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
MilkDetected but not QuantifiedNot QuantifiedNot SpecifiedNot Specified
Normal		 details
MilkDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
MilkDetected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal details
Abnormal Concentrations
Not Available
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB094021
KNApSAcK IDNot Available
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound25240460
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Jensen RG, Ferris AM, Lammi-Keefe CJ: The composition of milk fat. J Dairy Sci. 1991 Sep;74(9):3228-43. doi: 10.3168/jds.S0022-0302(91)78509-3. [PubMed:1779072 ]
  2. Mottram HR, Evershed RP: Elucidation of the composition of bovine milk fat triacylglycerols using high-performance liquid chromatography-atmospheric pressure chemical ionisation mass spectrometry. J Chromatogr A. 2001 Aug 17;926(2):239-53. [PubMed:11556330 ]
  3. 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 ]