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Record Information
Version4.0
StatusPredicted
Creation Date2017-09-16 22:44:15 UTC
Update Date2019-07-23 09:53:32 UTC
HMDB IDHMDB0130168
Secondary Accession NumbersNone
Metabolite Identification
Common Name3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one
Description3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one is a predicted metabolite generated by BioTransformer¹ that is produced by the metabolism of 5,6,7-trihydroxy-2-(4-methoxyphenyl)-3,4-dihydro-2h-1-benzopyran-4-one. It is generated by unspecified-gutmicro enzyme via a flavanone-c-ring-fission reaction. This flavanone-c-ring-fission occurs in human gut microbiota.
Structure
Data?1563875612
SynonymsNot Available
Chemical FormulaC16H14O6
Average Molecular Weight302.282
Monoisotopic Molecular Weight302.079038171
IUPAC Name3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one
Traditional Name3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one
CAS Registry NumberNot Available
SMILES
COC1=CC=C(C=CC(=O)C2=C(O)C(O)=C(O)C=C2O)C=C1
InChI Identifier
InChI=1S/C16H14O6/c1-22-10-5-2-9(3-6-10)4-7-11(17)14-12(18)8-13(19)15(20)16(14)21/h2-8,18-21H,1H3
InChI KeyDUJFBATXDTXVIO-UHFFFAOYSA-N
Chemical Taxonomy
DescriptionThis compound belongs to the class of organic compounds known as 2'-hydroxychalcones. These are organic compounds containing chalcone skeleton that carries a hydroxyl group at the 2'-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassLinear 1,3-diarylpropanoids
Sub ClassChalcones and dihydrochalcones
Direct Parent2'-Hydroxychalcones
Alternative Parents
Substituents
  • 2'-hydroxychalcone
  • Cinnamylphenol
  • Acylphloroglucinol derivative
  • Benzenetriol
  • Anisole
  • Methoxybenzene
  • Phenol ether
  • Aryl ketone
  • Phenoxy compound
  • Styrene
  • Benzoyl
  • Alkyl aryl ether
  • 1-hydroxy-4-unsubstituted benzenoid
  • Phenol
  • 1-hydroxy-2-unsubstituted benzenoid
  • Monocyclic benzene moiety
  • Benzenoid
  • Acryloyl-group
  • Vinylogous acid
  • Alpha,beta-unsaturated ketone
  • Enone
  • Ketone
  • Polyol
  • Ether
  • Organic oxide
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External DescriptorsNot Available
Ontology
Disposition

Source:

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
logP2.93ALOGPS
logP3.82ChemAxon
logS-3.5ALOGPS
pKa (Strongest Acidic)7.33ChemAxon
pKa (Strongest Basic)-4.8ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count6ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area107.22 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity81.26 m³·mol⁻¹ChemAxon
Polarizability30.4 ųChemAxon
Number of Rings2ChemAxon
Bioavailability1ChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleYesChemAxon
MDDR-like RuleYesChemAxon
Spectra
Spectrum TypeDescriptionSplash KeyView
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (4 TMS) - 70eV, Positivesplash10-004i-0000190000-fadc74870780b7526669JSpectraViewer | MoNA
Predicted GC-MSPredicted GC-MS Spectrum - GC-MS (Non-derivatized) - 70eV, Positivesplash10-00s9-0691000000-65cd6672a87cf2025e42JSpectraViewer | MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Positivesplash10-0udi-0429000000-effd1348bb6c4e94d6a6JSpectraViewer | MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Positivesplash10-0wu0-0922000000-9f6d420abcdb7cc9ba58JSpectraViewer | MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Positivesplash10-0gx3-3910000000-387121c4dbbfaff6d435JSpectraViewer | MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 10V, Negativesplash10-0udi-0319000000-286bff13a678cde5fa59JSpectraViewer | MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 20V, Negativesplash10-0f6x-0922000000-80ec6eea62e35adaa16fJSpectraViewer | MoNA
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 40V, Negativesplash10-00dm-3930000000-543a00acb9efb3fcfec7JSpectraViewer | MoNA
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
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. Djoumbou Feunang, Yannick (2017). Cheminformatics Tools for Enabling Metabolomics, 2017 (PhD thesis). University of Alberta.

Enzymes

General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:
UGT1A1
Uniprot ID:
P22309
Molecular weight:
59590.91
Reactions
3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one → 3,4,5-trihydroxy-6-{3,4,5-trihydroxy-2-[3-(4-methoxyphenyl)prop-2-enoyl]phenoxy}oxane-2-carboxylic aciddetails
3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one → 3,4,5-trihydroxy-6-{2,3,5-trihydroxy-4-[3-(4-methoxyphenyl)prop-2-enoyl]phenoxy}oxane-2-carboxylic aciddetails
3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one → 3,4,5-trihydroxy-6-{2,4,6-trihydroxy-3-[3-(4-methoxyphenyl)prop-2-enoyl]phenoxy}oxane-2-carboxylic aciddetails
3-(4-methoxyphenyl)-1-(2,3,4,6-tetrahydroxyphenyl)prop-2-en-1-one → 3,4,5-trihydroxy-6-{2,3,5-trihydroxy-6-[3-(4-methoxyphenyl)prop-2-enoyl]phenoxy}oxane-2-carboxylic aciddetails