DG(14:0/16:1(9Z)/0:0) (YMDB01125)

Identification
YMDB IDYMDB01125
NameDG(14:0/16:1(9Z)/0:0)
SpeciesSaccharomyces cerevisiae
StrainBrewer's yeast
DescriptionDG(14:0/16:1(9Z)/0:0) belongs to the family of Diacylglycerols. These are glycerolipids lipids containing a common glycerol backbone to which at least one fatty acyl group is esterified. DG(14:0/16:1(9Z)/0:0) is also a substrate of diacylglycerol kinase. It is involved in the phospholipid metabolic pathway.
Structure
Thumb
MOLSDFPDBSMILESInChI
Synonyms
  • 1-myristoyl-2-palmitoleoyl-sn-glycerol
  • DAG(14:0/16:1)
  • DAG(14:0/16:1n7)
  • DAG(14:0/16:1w7)
  • DAG(30:1)
  • DG(14:0/16:1)
  • DG(14:0/16:1n7)
  • DG(14:0/16:1w7)
  • DG(30:1)
  • Diacylglycerol
  • Diacylglycerol(14:0/16:1)
  • Diacylglycerol(14:0/16:1n7)
  • Diacylglycerol(14:0/16:1w7)
  • Diacylglycerol(30:1)
  • Diglyceride
CAS number3738-74-7
WeightAverage: 538.854
Monoisotopic: 538.459725096
InChI KeySSKSBJYFDDMVGX-UFOOELKISA-N
InChIInChI=1S/C33H62O5/c1-3-5-7-9-11-13-15-16-18-20-22-24-26-28-33(36)38-31(29-34)30-37-32(35)27-25-23-21-19-17-14-12-10-8-6-4-2/h13,15,31,34H,3-12,14,16-30H2,1-2H3/b15-13-/t31-/m1/s1
IUPAC Name(2R)-1-hydroxy-3-(tetradecanoyloxy)propan-2-yl (9Z)-hexadec-9-enoate
Traditional IUPAC Name(2R)-1-hydroxy-3-(tetradecanoyloxy)propan-2-yl (9Z)-hexadec-9-enoate
Chemical FormulaC33H62O5
SMILES[H][C@@](CO)(COC(=O)CCCCCCCCCCCCC)OC(=O)CCCCCCC\C=C/CCCCCC
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
StateSolid
Charge0
Melting pointNot Available
Experimental Properties
PropertyValueReference
Water SolubilityNot AvailablePhysProp
LogPNot AvailablePhysProp
Predicted Properties
PropertyValueSource
Water Solubility2.3e-05 g/LALOGPS
logP9.46ALOGPS
logP10.75ChemAxon
logS-7.4ALOGPS
pKa (Strongest Acidic)14.58ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count3ChemAxon
Hydrogen Donor Count1ChemAxon
Polar Surface Area72.83 ŲChemAxon
Rotatable Bond Count31ChemAxon
Refractivity159.61 m³·mol⁻¹ChemAxon
Polarizability70.21 ųChemAxon
Number of Rings0ChemAxon
Bioavailability0ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Biological Properties
Cellular LocationsNot Available
Organoleptic PropertiesNot Available
SMPDB Pathways
Triacylglycerol metabolism TG(14:0/14:0/16:1(9Z))PW007665 ThumbThumb?image type=greyscaleThumb?image type=simple
Triacylglycerol metabolism TG(14:0/14:1(9Z)/16:1(9Z))PW007673 ThumbThumb?image type=greyscaleThumb?image type=simple
Triacylglycerol metabolism TG(14:0/15:0/16:1(9Z))PW007688 ThumbThumb?image type=greyscaleThumb?image type=simple
Triacylglycerol metabolism TG(14:0/16:0/16:1(9Z))PW007725 ThumbThumb?image type=greyscaleThumb?image type=simple
Triacylglycerol metabolism TG(14:0/16:1(9Z)/16:1(9Z))PW007735 ThumbThumb?image type=greyscaleThumb?image type=simple
KEGG PathwaysNot Available
SMPDB ReactionsNot Available
KEGG ReactionsNot Available
Concentrations
Intracellular Concentrations
Intracellular ConcentrationSubstrateGrowth ConditionsStrainCitation
89000 ± 7575 umol/L SD media with 2% raffinose24 oCBY4741PMID: 19174513
Conversion Details Here
Extracellular ConcentrationsNot Available
Spectra
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-01p9-0094030000-0faefd377cf43f306953JSpectraViewer
References
References:
  • Ejsing, C. S., Sampaio, J. L., Surendranath, V., Duchoslav, E., Ekroos, K., Klemm, R. W., Simons, K., Shevchenko, A. (2009). "Global analysis of the yeast lipidome by quantitative shotgun mass spectrometry." Proc Natl Acad Sci U S A 106:2136-2141.19174513
Synthesis Reference:Not Available
External Links:
ResourceLink
CHEBI IDNot Available
HMDB IDHMDB07012
Pubchem Compound ID1324
Kegg IDC00165
ChemSpider ID24765846
FOODB IDNot Available
Wikipedia IDNot Available
BioCyc IDNot Available