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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 01:52:31 UTC
Update Date2022-03-07 02:56:34 UTC
HMDB IDHMDB0040344
Secondary Accession Numbers
  • HMDB40344
Metabolite Identification
Common Name3,5,6-Trihydroxy-3',4',7-trimethoxyflavone
Description3,5,6-Trihydroxy-3',4',7-trimethoxyflavone belongs to the class of organic compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position. Thus, 3,5,6-trihydroxy-3',4',7-trimethoxyflavone is considered to be a flavonoid. 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone has been detected, but not quantified in, citrus. This could make 3,5,6-trihydroxy-3',4',7-trimethoxyflavone a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone.
Structure
Data?1563863541
Synonyms
ValueSource
3,5,6-Trihydroxy-3',4',7'-trimethoxyflavoneHMDB, MeSH
Quercetagetin 7,3',4'-trimethyl etherHMDB
ThtmofHMDB
3',5,6-TH-TMFMeSH, HMDB
3',5,6-Trihydroxy-3,4',7-trimethoxyflavoneMeSH, HMDB
Chemical FormulaC18H16O8
Average Molecular Weight360.3148
Monoisotopic Molecular Weight360.084517488
IUPAC Name2-(3,4-dimethoxyphenyl)-3,5,6-trihydroxy-7-methoxy-4H-chromen-4-one
Traditional Name2-(3,4-dimethoxyphenyl)-3,5,6-trihydroxy-7-methoxychromen-4-one
CAS Registry Number99499-83-9
SMILES
COC1=C(O)C(O)=C2C(=O)C(O)=C(OC2=C1)C1=CC(OC)=C(OC)C=C1
InChI Identifier
InChI=1S/C18H16O8/c1-23-9-5-4-8(6-10(9)24-2)18-17(22)16(21)13-11(26-18)7-12(25-3)14(19)15(13)20/h4-7,19-20,22H,1-3H3
InChI KeyCZPFBNZMODZHIK-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonols. Flavonols are compounds that contain a flavone (2-phenyl-1-benzopyran-4-one) backbone carrying a hydroxyl group at the 3-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavones
Direct ParentFlavonols
Alternative Parents
Substituents
  • 7-methoxyflavonoid-skeleton
  • 3-hydroxyflavone
  • 4p-methoxyflavonoid-skeleton
  • 3p-methoxyflavonoid-skeleton
  • Hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 6-hydroxyflavonoid
  • 3-hydroxyflavonoid
  • Chromone
  • O-dimethoxybenzene
  • Dimethoxybenzene
  • 1-benzopyran
  • Benzopyran
  • Methoxybenzene
  • Anisole
  • Phenol ether
  • Phenoxy compound
  • 1-hydroxy-4-unsubstituted benzenoid
  • Alkyl aryl ether
  • Pyranone
  • Benzenoid
  • Pyran
  • Monocyclic benzene moiety
  • Vinylogous acid
  • Heteroaromatic compound
  • Oxacycle
  • Organoheterocyclic compound
  • Polyol
  • Ether
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Organic oxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water Solubility125.7 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.077 g/LALOGPS
logP2.25ALOGPS
logP2.29ChemAxon
logS-3.7ALOGPS
pKa (Strongest Acidic)8.3ChemAxon
pKa (Strongest Basic)-4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count8ChemAxon
Hydrogen Donor Count3ChemAxon
Polar Surface Area114.68 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity92.29 m³·mol⁻¹ChemAxon
Polarizability35.67 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+183.40430932474
DeepCCS[M-H]-181.04630932474
DeepCCS[M-2H]-215.0330932474
DeepCCS[M+Na]+190.15830932474
AllCCS[M+H]+182.932859911
AllCCS[M+H-H2O]+179.632859911
AllCCS[M+NH4]+185.932859911
AllCCS[M+Na]+186.732859911
AllCCS[M-H]-183.632859911
AllCCS[M+Na-2H]-183.132859911
AllCCS[M+HCOO]-182.832859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
3,5,6-Trihydroxy-3',4',7-trimethoxyflavoneCOC1=C(O)C(O)=C2C(=O)C(O)=C(OC2=C1)C1=CC(OC)=C(OC)C=C15037.6Standard polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavoneCOC1=C(O)C(O)=C2C(=O)C(O)=C(OC2=C1)C1=CC(OC)=C(OC)C=C13437.8Standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavoneCOC1=C(O)C(O)=C2C(=O)C(O)=C(OC2=C1)C1=CC(OC)=C(OC)C=C13496.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,1TMS,isomer #1COC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC)C=C3O2)C=C1OC3412.2Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,1TMS,isomer #2COC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC)C=C3O2)C=C1OC3385.7Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,1TMS,isomer #3COC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O)=C(OC)C=C3O2)C=C1OC3349.3Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,2TMS,isomer #1COC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC)C=C3O2)C=C1OC3268.5Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,2TMS,isomer #2COC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C)=C(OC)C=C3O2)C=C1OC3244.6Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,2TMS,isomer #3COC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O)=C(OC)C=C3O2)C=C1OC3249.9Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,3TMS,isomer #1COC1=CC=C(C2=C(O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C(OC)C=C3O2)C=C1OC3161.2Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,1TBDMS,isomer #1COC1=CC=C(C2=C(O)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC)C=C3O2)C=C1OC3637.6Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,1TBDMS,isomer #2COC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC)C=C3O2)C=C1OC3638.5Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,1TBDMS,isomer #3COC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O)=C(OC)C=C3O2)C=C1OC3594.4Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,2TBDMS,isomer #1COC1=CC=C(C2=C(O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C(OC)C=C3O2)C=C1OC3757.7Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,2TBDMS,isomer #2COC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C(O[Si](C)(C)C(C)(C)C)=C(OC)C=C3O2)C=C1OC3744.8Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,2TBDMS,isomer #3COC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O)=C(OC)C=C3O2)C=C1OC3745.9Semi standard non polar33892256
3,5,6-Trihydroxy-3',4',7-trimethoxyflavone,3TBDMS,isomer #1COC1=CC=C(C2=C(O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C(OC)C=C3O2)C=C1OC3853.5Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone GC-MS (Non-derivatized) - 70eV, Positivesplash10-001j-0409000000-2aeade731395861214c02017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone GC-MS (3 TMS) - 70eV, Positivesplash10-0ik9-2032090000-70fa078c9c6de1e2eeba2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 10V, Positive-QTOFsplash10-03di-0009000000-c163d5c7ff68fa7df4e52015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 20V, Positive-QTOFsplash10-03di-0109000000-17b8d4cdd86eef3b74872015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 40V, Positive-QTOFsplash10-0fza-2943000000-38832f3c754f2c6eb4c22015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 10V, Negative-QTOFsplash10-0a4i-0009000000-a324001104244a7dab342015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 20V, Negative-QTOFsplash10-0a4l-0119000000-1b66c71d55b7a4a276022015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 40V, Negative-QTOFsplash10-01w0-2494000000-23c6ad2c0dc49066a2392015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 10V, Positive-QTOFsplash10-03di-0009000000-ef0e36da9abfe27aa0762021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 20V, Positive-QTOFsplash10-03di-0009000000-3a7080e18a7609ec9fe72021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 40V, Positive-QTOFsplash10-02ai-2904000000-285f1d4e1c30a7a028d02021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 10V, Negative-QTOFsplash10-0a4i-0009000000-2a67be2cdf836654ba922021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 20V, Negative-QTOFsplash10-0a4i-0339000000-f26a0e1f330eeb7e8d452021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 3,5,6-Trihydroxy-3',4',7-trimethoxyflavone 40V, Negative-QTOFsplash10-067r-1921000000-f2a339462b1b18ae9bb52021-09-22Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
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
FooDB IDFDB020069
KNApSAcK IDC00004700
Chemspider ID4479671
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound5322091
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1882761
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .