Showing metabocard for DG(14:0/20:1(11Z)/0:0)[iso2] (BMDB0062611)

IdentificationTaxonomyPhysical propertiesSpectraConcentrationsLinksReferencesXML
Record Information
Version1.0
Creation Date2018-08-29 17:08:44 UTC
Update Date2020-06-04 20:13:56 UTC
MCDB ID BMDB0062611
Secondary Accession Numbers
  • BMDB62611
Metabolite Identification
Common NameDG(14:0/20:1(11Z)/0:0)[iso2]
DescriptionDG(14:0/20:1(11Z)/0:0), also known as DG(14:0/20:1) or diacylglycerol(34:1), belongs to the class of organic compounds known as 1,2-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 2. Thus, DG(14:0/20:1(11Z)/0:0) is considered to be a diradylglycerol lipid molecule. DG(14:0/20:1(11Z)/0:0) is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. DG(14:0/20:1(11Z)/0:0) participates in a number of enzymatic reactions, within cattle. In particular, DG(14:0/20:1(11Z)/0:0) can be biosynthesized from PA(14:0/20:1(11Z)); which is catalyzed by the enzyme phosphatidate phosphatase. Furthermore, DG(14:0/20:1(11Z)/0:0) and gondoyl-CoA can be converted into TG(14:0/20:1(11Z)/20:1(11Z)); which is catalyzed by the enzyme diacylglycerol O-acyltransferase. Furthermore, DG(14:0/20:1(11Z)/0:0) can be biosynthesized from PA(14:0/20:1(11Z)) through the action of the enzyme phosphatidate phosphatase. Furthermore, DG(14:0/20:1(11Z)/0:0) and docosanoyl-CoA can be converted into TG(14:0/20:1(11Z)/22:0) through the action of the enzyme diacylglycerol O-acyltransferase. Furthermore, DG(14:0/20:1(11Z)/0:0) can be biosynthesized from PA(14:0/20:1(11Z)); which is catalyzed by the enzyme phosphatidate phosphatase. Finally, DG(14:0/20:1(11Z)/0:0) and clupanodonoyl-CoA can be converted into TG(14:0/20:1(11Z)/22:5(7Z,10Z,13Z,16Z,19Z)); which is catalyzed by the enzyme diacylglycerol O-acyltransferase. In cattle, DG(14:0/20:1(11Z)/0:0) is involved in a few metabolic pathways, which include de novo triacylglycerol biosynthesis TG(14:0/20:1(11Z)/20:1(11Z)) pathway, de novo triacylglycerol biosynthesis TG(14:0/20:1(11Z)/22:0) pathway, and de novo triacylglycerol biosynthesis TG(14:0/20:1(11Z)/22:5(7Z,10Z,13Z,16Z,19Z)) pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
SynonymsNot Available
Chemical FormulaC37H70O5
Average Molecular Weight594.962
Monoisotopic Molecular Weight594.522325354
IUPAC Name(2R)-1-hydroxy-3-(tetradecanoyloxy)propan-2-yl (11Z)-icos-11-enoate
Traditional Name(2R)-1-hydroxy-3-(tetradecanoyloxy)propan-2-yl (11Z)-icos-11-enoate
CAS Registry NumberNot Available
SMILES
[H][C@@](CO)(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCCCC\C=C/CCCCCCCC
InChI Identifier
InChI=1S/C37H70O5/c1-3-5-7-9-11-13-15-16-17-18-19-20-22-24-26-28-30-32-37(40)42-35(33-38)34-41-36(39)31-29-27-25-23-21-14-12-10-8-6-4-2/h16-17,35,38H,3-15,18-34H2,1-2H3/b17-16-/t35-/m1/s1
InChI KeyVQOIASKPUKUIDV-XHYHITGYSA-N
Chemical Taxonomy
Description belongs to the class of organic compounds known as 1,2-diacylglycerols. These are diacylglycerols containing a glycerol acylated at positions 1 and 2.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassGlycerolipids
Sub ClassDiradylglycerols
Direct Parent1,2-diacylglycerols
Alternative Parents
Substituents
  • 1,2-acyl-sn-glycerol
  • Fatty acid ester
  • Fatty acyl
  • Dicarboxylic acid or derivatives
  • Carboxylic acid ester
  • Carboxylic acid derivative
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Primary alcohol
  • Organooxygen compound
  • Carbonyl group
  • Alcohol
  • Aliphatic acyclic compound
Molecular FrameworkAliphatic acyclic compounds
External DescriptorsNot Available
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
logP10.1ALOGPS
logP12.53ChemAxon
logS-7.5ALOGPS
pKa (Strongest Acidic)14.58ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area72.83 ŲChemAxon
Rotatable Bond Count35ChemAxon
Refractivity178.02 m³·mol⁻¹ChemAxon
Polarizability78.7 ųChemAxon
Number of Rings0ChemAxon
Bioavailability0ChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Spectra
Spectrum TypeDescriptionSplash KeyDeposition DateView
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (TMS_1_1) - 70eV, PositiveNot Available2022-08-08View Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0gbu-0059002000-db63532d3d87fe9f99712016-09-19View Spectrum
Concentrations
StatusValueReferenceDetails
Detected and Quantified33 +/- 1 uM details
Detected and Quantified42 +/- 1 uM details
Detected and Quantified55 +/- 2 uM details
Detected and Quantified10 +/- 1 uM details
HMDB IDNot Available
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB 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 CompoundNot Available
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. 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.