Record Information
Version1.0
Creation date2010-04-08 22:14:09 UTC
Update date2019-11-26 03:17:07 UTC
Primary IDFDB019119
Secondary Accession NumbersNot Available
Chemical Information
FooDB Namexi-p-Coumaric acid 4-glucoside
Descriptiontrans-p-Coumaric acid 4-glucoside belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. trans-p-Coumaric acid 4-glucoside has been detected, but not quantified in, loquats (Eriobotrya japonica). This could make trans-p-coumaric acid 4-glucoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on trans-p-Coumaric acid 4-glucoside.
CAS Number14364-05-7
Structure
Thumb
Synonyms
SynonymSource
trans-p-Coumarate 4-glucosideGenerator
3-(4-(beta-D-Glucopyranosyloxy)phenyl)-2-propenoic acidHMDB
3-[4-(beta-D-Glucopyranosyloxy)phenyl]acrylic acidHMDB
3-[4-(beta-D-Glucopyranosyloxy)phenyl]prop-2-enoic acidHMDB
4-O-beta-D-Glucosyl-4-coumaric acidHMDB
4-O-beta-D-Glucosyl-4-hydroxycinnamateHMDB
4-O-[4-(2-Carboxyvinyl)phenyl]-beta-D-glucopyranoseHMDB
(2E)-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoateGenerator
cis-p-Coumarate 4-glucosideGenerator
2-Propenoic acid, 3-(4-(beta-D-glucopyranosyloxy)phenyl)-biospider
3-[4-(beta-D-glucopyranosyloxy)phenyl]acrylic acidbiospider
3-[4-(beta-D-glucopyranosyloxy)phenyl]prop-2-enoic acidbiospider
4-O-[4-(2-carboxyvinyl)phenyl]-beta-D-glucopyranosebiospider
4-O-beta-D-glucosyl-4-coumaric acidbiospider
Predicted Properties
PropertyValueSource
Water Solubility5.08 g/LALOGPS
logP-0.35ALOGPS
logP-0.44ChemAxon
logS-1.8ALOGPS
pKa (Strongest Acidic)3.72ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count5ChemAxon
Polar Surface Area136.68 ŲChemAxon
Rotatable Bond Count5ChemAxon
Refractivity77.19 m³·mol⁻¹ChemAxon
Polarizability31.85 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Chemical FormulaC15H18O8
IUPAC name(2E)-3-(4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoic acid
InChI IdentifierInChI=1S/C15H18O8/c16-7-10-12(19)13(20)14(21)15(23-10)22-9-4-1-8(2-5-9)3-6-11(17)18/h1-6,10,12-16,19-21H,7H2,(H,17,18)/b6-3+
InChI KeyLJFYQZQUAULRDF-ZZXKWVIFSA-N
Isomeric SMILESOCC1OC(OC2=CC=C(\C=C\C(O)=O)C=C2)C(O)C(O)C1O
Average Molecular Weight326.2986
Monoisotopic Molecular Weight326.100167552
Classification
Description Belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentPhenolic glycosides
Alternative Parents
Substituents
  • Phenolic glycoside
  • Cinnamic acid
  • Cinnamic acid or derivatives
  • Hexose monosaccharide
  • O-glycosyl compound
  • Phenoxy compound
  • Phenol ether
  • Styrene
  • Monocyclic benzene moiety
  • Monosaccharide
  • Oxane
  • Benzenoid
  • Secondary alcohol
  • Organoheterocyclic compound
  • Monocarboxylic acid or derivatives
  • Oxacycle
  • Carboxylic acid
  • Carboxylic acid derivative
  • Acetal
  • Polyol
  • Alcohol
  • Hydrocarbon derivative
  • Organic oxide
  • Carbonyl group
  • Primary alcohol
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Route of exposure:

Source:

Biological location:

Role

Biological role:

Physico-Chemical Properties - Experimental
Physico-Chemical Properties - Experimental
PropertyValueReference
Physical stateNot Available
Physical DescriptionNot Available
Mass CompositionC 55.21%; H 5.56%; O 39.23%DFC
Melting PointNot Available
Boiling PointNot Available
Experimental Water SolubilityNot Available
Experimental logPNot Available
Experimental pKaNot Available
Isoelectric pointNot Available
ChargeNot Available
Optical RotationNot Available
Spectroscopic UV DataNot Available
DensityNot Available
Refractive IndexNot Available
Spectra
Spectra
EI-MS/GC-MS
TypeDescriptionSplash KeyView
Predicted GC-MSxi-p-Coumaric acid 4-glucoside, non-derivatized, Predicted GC-MS Spectrum - 70eV, Positivesplash10-0zfr-5943000000-c492ad4cea7748c10d1dSpectrum
Predicted GC-MSxi-p-Coumaric acid 4-glucoside, 5 TMS, Predicted GC-MS Spectrum - 70eV, Positivesplash10-00di-1020229000-cd5e122c29a7c414bbb3Spectrum
Predicted GC-MSxi-p-Coumaric acid 4-glucoside, non-derivatized, Predicted GC-MS Spectrum - 70eV, PositiveNot AvailableSpectrum
MS/MS
TypeDescriptionSplash KeyView
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0691-0935000000-c974f539415af8bc2656Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-014j-0910000000-2b9e08298c82be733463Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-00kb-1900000000-301e2a0a8e986454b07eSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-01t9-1928000000-664ca3f5aa531f156b9fSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-03di-1911000000-33266a1715378857682aSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-03xs-3900000000-6a847d57baead9a24cf2Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-00or-0906000000-ff40c38471b820f5cd46Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-02t9-2920000000-9836ca930b3e9ff1b7efSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-014i-0900000000-8cc86ba16bb3961ac899Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0002-0906000000-b01d52f59a8d17a35095Spectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0a4i-0694000000-5fd94da869aa357b76dcSpectrum
Predicted MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0uxr-2910000000-f71f5d773ce8ae94144eSpectrum
NMRNot Available
ChemSpider IDNot Available
ChEMBL IDNot Available
KEGG Compound IDNot Available
Pubchem Compound ID13783633
Pubchem Substance IDNot Available
ChEBI IDNot Available
Phenol-Explorer IDNot Available
DrugBank IDNot Available
HMDB IDNot Available
CRC / DFC (Dictionary of Food Compounds) IDCMP73-U:LPD99-O
EAFUS IDNot Available
Dr. Duke IDNot Available
BIGG IDNot Available
KNApSAcK IDNot Available
HET IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
Flavornet IDNot Available
GoodScent IDNot Available
SuperScent IDNot Available
Wikipedia IDNot Available
Phenol-Explorer Metabolite IDNot Available
Duplicate IDSNot Available
Old DFC IDSNot Available
Associated Foods
FoodContent Range AverageReference
FoodReference
Biological Effects and Interactions
Health Effects / BioactivitiesNot Available
EnzymesNot Available
PathwaysNot Available
MetabolismNot Available
BiosynthesisNot Available
Organoleptic Properties
FlavoursNot Available
Files
MSDSNot Available
References
Synthesis ReferenceNot Available
General ReferenceNot Available
Content Reference