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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 02:14:51 UTC
Update Date2022-03-07 02:56:41 UTC
HMDB IDHMDB0040675
Secondary Accession Numbers
  • HMDB40675
Metabolite Identification
Common NameArtonin J
DescriptionArtonin J belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring. Thus, artonin J is considered to be a flavonoid lipid molecule. Artonin J is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Outside of the human body, artonin J has been detected, but not quantified in, fruits and jackfruits. This could make artonin J a potential biomarker for the consumption of these foods.
Structure
Data?1563863576
SynonymsNot Available
Chemical FormulaC25H24O7
Average Molecular Weight436.4539
Monoisotopic Molecular Weight436.152203122
IUPAC Name6,8,17,19-tetrahydroxy-14,14-dimethyl-18-(3-methylbut-2-en-1-yl)-3,15-dioxapentacyclo[11.6.1.0²,¹¹.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one
Traditional Name6,8,17,19-tetrahydroxy-14,14-dimethyl-18-(3-methylbut-2-en-1-yl)-3,15-dioxapentacyclo[11.6.1.0²,¹¹.0⁴,⁹.0¹⁶,²⁰]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one
CAS Registry Number148719-51-1
SMILES
CC(C)=CCC1=C(O)C2=C3C(CC4=C2OC2=CC(O)=CC(O)=C2C4=O)C(C)(C)OC3=C1O
InChI Identifier
InChI=1S/C25H24O7/c1-10(2)5-6-12-20(28)19-17-14(25(3,4)32-24(17)22(12)30)9-13-21(29)18-15(27)7-11(26)8-16(18)31-23(13)19/h5,7-8,14,26-28,30H,6,9H2,1-4H3
InChI KeyWQIPFMCXBWXUAV-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as xanthones. These are polycyclic aromatic compounds containing a xanthene moiety conjugated to a ketone group at carbon 9. Xanthene is a tricyclic compound made up of two benzene rings linearly fused to each other through a pyran ring.
KingdomOrganic compounds
Super ClassOrganoheterocyclic compounds
ClassBenzopyrans
Sub Class1-benzopyrans
Direct ParentXanthones
Alternative Parents
Substituents
  • Naphthopyranone
  • Xanthone
  • Naphthopyran
  • Chromone
  • 1-naphthol
  • Naphthalene
  • Coumaran
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Alkyl aryl ether
  • Pyranone
  • Benzenoid
  • Pyran
  • Vinylogous acid
  • Heteroaromatic compound
  • Polyol
  • Oxacycle
  • Ether
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point281 - 282 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.011 g/LALOGPS
logP4.07ALOGPS
logP4.56ChemAxon
logS-4.6ALOGPS
pKa (Strongest Acidic)-8.2ChemAxon
pKa (Strongest Basic)13.93ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area116.45 ŲChemAxon
Rotatable Bond Count2ChemAxon
Refractivity120.39 m³·mol⁻¹ChemAxon
Polarizability46.88 ųChemAxon
Number of Rings5ChemAxon
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]+201.66330932474
DeepCCS[M-H]-199.30530932474
DeepCCS[M-2H]-232.54530932474
DeepCCS[M+Na]+208.25630932474
AllCCS[M+H]+204.432859911
AllCCS[M+H-H2O]+201.932859911
AllCCS[M+NH4]+206.632859911
AllCCS[M+Na]+207.332859911
AllCCS[M-H]-205.732859911
AllCCS[M+Na-2H]-205.632859911
AllCCS[M+HCOO]-205.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Artonin JCC(C)=CCC1=C(O)C2=C3C(CC4=C2OC2=CC(O)=CC(O)=C2C4=O)C(C)(C)OC3=C1O5586.6Standard polar33892256
Artonin JCC(C)=CCC1=C(O)C2=C3C(CC4=C2OC2=CC(O)=CC(O)=C2C4=O)C(C)(C)OC3=C1O3479.3Standard non polar33892256
Artonin JCC(C)=CCC1=C(O)C2=C3C(CC4=C2OC2=CC(O)=CC(O)=C2C4=O)C(C)(C)OC3=C1O4005.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Artonin J,1TMS,isomer #1CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O)C=C2O13680.6Semi standard non polar33892256
Artonin J,1TMS,isomer #2CC(C)=CCC1=C(O)C2=C3C(=C1O)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O[Si](C)(C)C)C=C2O13697.1Semi standard non polar33892256
Artonin J,1TMS,isomer #3CC(C)=CCC1=C(O)C2=C3C(=C1O)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C)C=C(O)C=C2O13649.4Semi standard non polar33892256
Artonin J,1TMS,isomer #4CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O)=CC(O)=C2C1=O3663.3Semi standard non polar33892256
Artonin J,2TMS,isomer #1CC(C)=CCC1=C(O[Si](C)(C)C)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O)C=C2O13608.7Semi standard non polar33892256
Artonin J,2TMS,isomer #2CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O[Si](C)(C)C)C=C2O13640.9Semi standard non polar33892256
Artonin J,2TMS,isomer #3CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C)C=C(O)C=C2O13591.4Semi standard non polar33892256
Artonin J,2TMS,isomer #4CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O[Si](C)(C)C)=CC(O)=C2C1=O3620.4Semi standard non polar33892256
Artonin J,2TMS,isomer #5CC(C)=CCC1=C(O)C2=C3C(=C1O)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C2O13617.9Semi standard non polar33892256
Artonin J,2TMS,isomer #6CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O)=CC(O[Si](C)(C)C)=C2C1=O3582.8Semi standard non polar33892256
Artonin J,3TMS,isomer #1CC(C)=CCC1=C(O[Si](C)(C)C)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O[Si](C)(C)C)C=C2O13587.5Semi standard non polar33892256
Artonin J,3TMS,isomer #2CC(C)=CCC1=C(O[Si](C)(C)C)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C)C=C(O)C=C2O13542.5Semi standard non polar33892256
Artonin J,3TMS,isomer #3CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C2O13624.8Semi standard non polar33892256
Artonin J,3TMS,isomer #4CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C2C1=O3569.1Semi standard non polar33892256
Artonin J,4TMS,isomer #1CC(C)=CCC1=C(O[Si](C)(C)C)C2=C3C(=C1O[Si](C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C2O13583.2Semi standard non polar33892256
Artonin J,1TBDMS,isomer #1CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O)C=C2O13896.0Semi standard non polar33892256
Artonin J,1TBDMS,isomer #2CC(C)=CCC1=C(O)C2=C3C(=C1O)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C2O13912.5Semi standard non polar33892256
Artonin J,1TBDMS,isomer #3CC(C)=CCC1=C(O)C2=C3C(=C1O)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C2O13868.2Semi standard non polar33892256
Artonin J,1TBDMS,isomer #4CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O)=CC(O)=C2C1=O3896.8Semi standard non polar33892256
Artonin J,2TBDMS,isomer #1CC(C)=CCC1=C(O[Si](C)(C)C(C)(C)C)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O)C=C2O14067.9Semi standard non polar33892256
Artonin J,2TBDMS,isomer #2CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C2O14095.5Semi standard non polar33892256
Artonin J,2TBDMS,isomer #3CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C2O14034.8Semi standard non polar33892256
Artonin J,2TBDMS,isomer #4CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C2C1=O4081.1Semi standard non polar33892256
Artonin J,2TBDMS,isomer #5CC(C)=CCC1=C(O)C2=C3C(=C1O)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C=C2O14069.6Semi standard non polar33892256
Artonin J,2TBDMS,isomer #6CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O4036.4Semi standard non polar33892256
Artonin J,3TBDMS,isomer #1CC(C)=CCC1=C(O[Si](C)(C)C(C)(C)C)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C2O14197.2Semi standard non polar33892256
Artonin J,3TBDMS,isomer #2CC(C)=CCC1=C(O[Si](C)(C)C(C)(C)C)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C2O14146.8Semi standard non polar33892256
Artonin J,3TBDMS,isomer #3CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C=C2O14260.5Semi standard non polar33892256
Artonin J,3TBDMS,isomer #4CC(C)=CCC1=C(O)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)OC(C)(C)C3CC1=C2OC2=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C2C1=O4209.7Semi standard non polar33892256
Artonin J,4TBDMS,isomer #1CC(C)=CCC1=C(O[Si](C)(C)C(C)(C)C)C2=C3C(=C1O[Si](C)(C)C(C)(C)C)C1=C(CC3C(C)(C)O2)C(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C=C2O14324.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Artonin J GC-MS (Non-derivatized) - 70eV, Positivesplash10-0596-4205900000-bf7ce86eea9f6cdd44642017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Artonin J GC-MS (3 TMS) - 70eV, Positivesplash10-000i-2100039000-a8bfa27a4c636de201f32017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Artonin J 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 - Artonin J 10V, Positive-QTOFsplash10-000i-0003900000-a83a21d911479df8fbac2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 20V, Positive-QTOFsplash10-015i-3019500000-1bf8bc05cc9b6283db842015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 40V, Positive-QTOFsplash10-02vi-6039000000-a1956de06632e909649a2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 10V, Negative-QTOFsplash10-000i-0000900000-d410f62deb4a790192e12015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 20V, Negative-QTOFsplash10-000i-0002900000-55afc4a6dd1ea659f06c2015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 40V, Negative-QTOFsplash10-016u-4229400000-e1c8c556beee3f5b66252015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 10V, Positive-QTOFsplash10-000i-0000900000-254037e1a9b2771bb2282021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 20V, Positive-QTOFsplash10-000i-0000900000-254037e1a9b2771bb2282021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 40V, Positive-QTOFsplash10-0f79-0720900000-67395067fc36538fdaf42021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 10V, Negative-QTOFsplash10-000i-0000900000-4d20ffee5876aaf4048d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 20V, Negative-QTOFsplash10-000i-0000900000-4d20ffee5876aaf4048d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Artonin J 40V, Negative-QTOFsplash10-0fb9-0609300000-5bc523fe2e44d9a9e9ef2021-09-23Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Membrane
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 IDFDB020472
KNApSAcK IDC00013481
Chemspider ID24844323
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound44258663
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
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.. .