Showing metabocard for DG(18:0/18:1(11Z)/0:0) (BMDB0007159)

IdentificationTaxonomyPhysical propertiesPathwaysSpectraConcentrationsLinksReferencesenzymes (2) Show 2 proteinsXML
Record Information
Version1.0
Creation Date2016-09-30 23:31:45 UTC
Update Date2020-05-21 16:27:45 UTC
BMDB IDBMDB0007159
Secondary Accession Numbers
  • BMDB07159
Metabolite Identification
Common NameDG(18:0/18:1(11Z)/0:0)
DescriptionDG(18:0/18:1(11Z)/0:0), also known as dg(18:0/18:1(11z)/0:0) or DAG(18:0/18:1), belongs to the class of organic compounds known as 1,2-dg(18:0/18:1(11z)/0:0)s. These are dg(18:0/18:1(11z)/0:0)s containing a glycerol acylated at positions 1 and 2. DG(18:0/18:1(11Z)/0:0) is possibly soluble (in water) and an extremely weak basic (essentially neutral) compound (based on its pKa). DG(18:0/18:1(11Z)/0:0) participates in a number of enzymatic reactions, within cattle. In particular, DG(18:0/18:1(11Z)/0:0) can be biosynthesized from PA(18:0/18:1(11Z)); which is mediated by the enzyme phosphatidate phosphatase. Furthermore, DG(18:0/18:1(11Z)/0:0) and oleoyl-CoA can be converted into TG(18:0/18:1(11Z)/18:1(9Z)) through its interaction with the enzyme dg(18:0/18:1(11z)/0:0) O-acyltransferase. Furthermore, DG(18:0/18:1(11Z)/0:0) can be biosynthesized from PA(18:0/18:1(11Z)); which is catalyzed by the enzyme phosphatidate phosphatase. Finally, DG(18:0/18:1(11Z)/0:0) and gamma-linolenoyl-CoA can be converted into TG(18:0/18:1(11Z)/18:3(6Z,9Z,12Z)) through its interaction with the enzyme dg(18:0/18:1(11z)/0:0) O-acyltransferase. In cattle, DG(18:0/18:1(11Z)/0:0) is involved in a couple of metabolic pathways, which include de novo triacylglycerol biosynthesis TG(18:0/18:1(11Z)/18:1(9Z)) pathway and de novo triacylglycerol biosynthesis TG(18:0/18:1(11Z)/18:3(6Z,9Z,12Z)) pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
ValueSource
DAG(36:1)Lipid Annotator, HMDB
DG(18:0/18:1(11Z)/0:0)Lipid Annotator
Diacylglycerol(36:1)Lipid Annotator, HMDB
DAG(18:0/18:1)Lipid Annotator, HMDB
DiglycerideLipid Annotator, HMDB
Diacylglycerol(18:0/18:1)Lipid Annotator, HMDB
DiacylglycerolLipid Annotator, HMDB
DG(18:0/18:1)Lipid Annotator, HMDB
1-stearoyl-2-vaccenoyl-sn-glycerolLipid Annotator, HMDB
1-octadecanoyl-2-(11Z-octadecenoyl)-sn-glycerolLipid Annotator, HMDB
DG(36:1)Lipid Annotator, HMDB
DAG(18:0/18:1N7)HMDB
DAG(18:0/18:1W7)HMDB
DG(18:0/18:1N7)HMDB
DG(18:0/18:1W7)HMDB
Diacylglycerol(18:0/18:1n7)HMDB
Diacylglycerol(18:0/18:1W7)HMDB
Chemical FormulaC39H74O5
Average Molecular Weight623.0019
Monoisotopic Molecular Weight622.553625478
IUPAC Name(2S)-1-hydroxy-3-(octadecanoyloxy)propan-2-yl (11Z)-octadec-11-enoate
Traditional Namediacylglycerol
CAS Registry NumberNot Available
SMILES
[H][C@](CO)(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCC\C=C/CCCCCC
InChI Identifier
InChI=1S/C39H74O5/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-38(41)43-36-37(35-40)44-39(42)34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h14,16,37,40H,3-13,15,17-36H2,1-2H3/b16-14-/t37-/m0/s1
InChI KeyYJORXFQCYXMMHL-KDKAWYBRSA-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
Ontology
StatusExpected but not Quantified
Origin
  • Endogenous
  • Exogenous
BiofunctionNot Available
ApplicationNot Available
Cellular locations
  • 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
logP10.34ALOGPS
logP13.42ChemAxon
logS-7.6ALOGPS
pKa (Strongest Acidic)14.58ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area72.83 ŲChemAxon
Rotatable Bond Count37ChemAxon
Refractivity187.22 m³·mol⁻¹ChemAxon
Polarizability81.5 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 (1 TMS) - 70eV, Positivesplash10-029i-4391446000-ed2227b5d77c37640c53View in MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (TBDMS_1_1) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS ("DG(18:0/18:1(11Z)/0:0),1TMS,#1" TMS) - 70eV, PositiveNot AvailableView in JSpectraViewer
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0000009000-fce9091ab20877af1859View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-052o-0009004000-31e141f7dec25acc8594View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000f-0009004000-8978ea08da2193fc6059View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-00dr-2057109000-bd386daa9473d916ad70View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014i-3296002000-acedd6f41f10584769a6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-014r-7697100000-081ee0587e4718774da7View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-0000009000-8b1291422a70b2640ab8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0002-0000009000-8b1291422a70b2640ab8View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-03di-0009000000-602c71feebdd81b7a4e6View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00di-1044009000-b06b88971a4a6bb66cbfView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-001i-2093000000-339bdaf2372dfce18ca0View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00lr-1191000000-318ba0d71ab598d50362View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0006-0000009000-bab9e83f09359631bc8fView in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-052o-0009004000-9f455557dd938e5b9983View in MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-000f-0009004000-818182964e61f6d27663View in MoNA
Biological Properties
Cellular Locations
  • Cell membrane
  • Membrane
Biospecimen Locations
  • All Tissues
Pathways
Normal Concentrations
BiospecimenStatusValueAgeSexConditionReferenceDetails
All TissuesExpected but not QuantifiedNot QuantifiedNot SpecifiedNot SpecifiedNormal
  • Not Applicable
 details
Abnormal Concentrations
Not Available
HMDB IDHMDB0007159
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDNot Available
KNApSAcK IDNot Available
Chemspider ID24765954
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound53478049
PDB IDNot Available
ChEBI IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available

Enzymes

Enzyme Details
1. Ethanolaminephosphotransferase 1
General function:
Involved in ethanolaminephosphotransferase activity
Specific function:
Catalyzes phosphatidylethanolamine biosynthesis from CDP-ethanolamine. It thereby plays a central role in the formation and maintenance of vesicular membranes. Involved in the foramtion of phosphatidylethanolamine via 'Kennedy' pathway (By similarity).
Gene Name:
SELENOI
Uniprot ID:
Q17QM4
Molecular weight:
45214.0
Reactions
CDP-Ethanolamine + DG(18:0/18:1(11Z)/0:0) → Cytidine monophosphate + PE(18:0/18:1(11Z))details
Enzyme Details
2. Diacylglycerol O-acyltransferase 1
General function:
Not Available
Specific function:
Catalyzes the terminal and only committed step in triacylglycerol synthesis by using diacylglycerol and fatty acyl CoA as substrates. In contrast to DGAT2 it is not essential for survival. May be involved in VLDL (very low density lipoprotein) assembly. Functions as the major acyl-CoA retinol acyltransferase (ARAT) in the skin, where it acts to maintain retinoid homeostasis and prevent retinoid toxicity leading to skin and hair disorders. In liver, plays a role in esterifying exogenous fatty acids to glycerol.
Gene Name:
DGAT1
Uniprot ID:
Q8MK44
Molecular weight:
55602.0
Reactions
DG(18:0/18:1(11Z)/0:0) + Oleoyl-CoA → TG(18:0/18:1(11Z)/18:1(9Z)) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Gamma-linolenoyl-CoA → TG(18:0/18:1(11Z)/18:3(6Z,9Z,12Z)) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Eicosanoyl-CoA → TG(18:0/18:1(11Z)/20:0) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Gondoyl-CoA → TG(18:0/18:1(11Z)/20:1(11Z)) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + 5Z,8Z,11Z,14Z-eicosatetraenonyl-CoA → TG(18:0/18:1(11Z)/20:4(5Z,8Z,11Z,14Z)) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Docosanoyl-CoA → TG(18:0/18:1(11Z)/22:0) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Erucoyl-CoA → TG(18:0/18:1(11Z)/22:1(13Z)) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Clupanodonyl CoA → TG(18:0/18:1(11Z)/22:5(7Z,10Z,13Z,16Z,19Z)) + Coenzyme Adetails
DG(18:0/18:1(11Z)/0:0) + Tetracosanoyl-CoA → TG(18:0/18:1(11Z)/24:0) + Coenzyme Adetails