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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:39:06 UTC
Update Date2022-03-07 02:52:42 UTC
HMDB IDHMDB0030797
Secondary Accession Numbers
  • HMDB30797
Metabolite Identification
Common NameMulberranol
DescriptionMulberranol belongs to the class of organic compounds known as 6-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 6-position. Based on a literature review very few articles have been published on Mulberranol.
Structure
Data?1563862039
SynonymsNot Available
Chemical FormulaC25H26O7
Average Molecular Weight438.4697
Monoisotopic Molecular Weight438.167853186
IUPAC Name7-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-2H,3H,5H-furo[3,2-g]chromen-5-one
Traditional Name7-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-2H,3H-furo[3,2-g]chromen-5-one
CAS Registry Number62393-99-1
SMILES
CC(C)=CCC1=C(OC2=C(C(O)=C3CC(OC3=C2)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C1
InChI Identifier
InChI=1S/C25H26O7/c1-12(2)5-7-15-22(28)21-19(32-24(15)14-8-6-13(26)9-17(14)27)11-18-16(23(21)29)10-20(31-18)25(3,4)30/h5-6,8-9,11,20,26-27,29-30H,7,10H2,1-4H3
InChI KeyFMKONXHUEWRDEL-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 6-prenylated flavones. These are flavones that features a C5-isoprenoid substituent at the 6-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavones
Direct Parent6-prenylated flavones
Alternative Parents
Substituents
  • 6-prenylated flavone
  • 3-prenylated flavone
  • Furanoflavone
  • Furanoflavonoid or dihydroflavonoid
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • Hydroxyflavonoid
  • Furanochromone
  • Chromone
  • Benzopyran
  • 1-benzopyran
  • Coumaran
  • Resorcinol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Alkyl aryl ether
  • Phenol
  • Pyranone
  • Monocyclic benzene moiety
  • Pyran
  • Benzenoid
  • Heteroaromatic compound
  • Vinylogous acid
  • Tertiary alcohol
  • Oxacycle
  • Organoheterocyclic compound
  • Ether
  • Organic oxygen compound
  • Hydrocarbon derivative
  • Organic oxide
  • Organooxygen compound
  • Alcohol
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water Solubility0.4 mg/L @ 25 °C (est)The Good Scents Company Information System
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.0073 g/LALOGPS
logP3.88ALOGPS
logP4.27ChemAxon
logS-4.8ALOGPS
pKa (Strongest Acidic)8.03ChemAxon
pKa (Strongest Basic)-3.1ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count7ChemAxon
Hydrogen Donor Count4ChemAxon
Polar Surface Area116.45 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity121.26 m³·mol⁻¹ChemAxon
Polarizability47.36 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+203.98331661259
DarkChem[M-H]-200.94631661259
DeepCCS[M+H]+208.48830932474
DeepCCS[M-H]-206.09330932474
DeepCCS[M-2H]-238.97630932474
DeepCCS[M+Na]+214.40130932474
AllCCS[M+H]+206.332859911
AllCCS[M+H-H2O]+203.832859911
AllCCS[M+NH4]+208.632859911
AllCCS[M+Na]+209.232859911
AllCCS[M-H]-207.132859911
AllCCS[M+Na-2H]-207.332859911
AllCCS[M+HCOO]-207.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
MulberranolCC(C)=CCC1=C(OC2=C(C(O)=C3CC(OC3=C2)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C15695.2Standard polar33892256
MulberranolCC(C)=CCC1=C(OC2=C(C(O)=C3CC(OC3=C2)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C13667.8Standard non polar33892256
MulberranolCC(C)=CCC1=C(OC2=C(C(O)=C3CC(OC3=C2)C(C)(C)O)C1=O)C1=C(O)C=C(O)C=C13928.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Mulberranol,1TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C)=C2C1=O3654.1Semi standard non polar33892256
Mulberranol,1TMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O)=C2C1=O3755.6Semi standard non polar33892256
Mulberranol,1TMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O)=C2C1=O3639.9Semi standard non polar33892256
Mulberranol,1TMS,isomer #4CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O)O3)C(O)=C2C1=O3683.1Semi standard non polar33892256
Mulberranol,2TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C)=C2C1=O3595.7Semi standard non polar33892256
Mulberranol,2TMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C)=C2C1=O3551.7Semi standard non polar33892256
Mulberranol,2TMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O[Si](C)(C)C)=C2C1=O3663.8Semi standard non polar33892256
Mulberranol,2TMS,isomer #4CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O)=C2C1=O3681.6Semi standard non polar33892256
Mulberranol,2TMS,isomer #5CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O)=C2C1=O3642.4Semi standard non polar33892256
Mulberranol,2TMS,isomer #6CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O)=C2C1=O3597.6Semi standard non polar33892256
Mulberranol,3TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C)=C2C1=O3570.5Semi standard non polar33892256
Mulberranol,3TMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O[Si](C)(C)C)=C2C1=O3611.9Semi standard non polar33892256
Mulberranol,3TMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O[Si](C)(C)C)=C2C1=O3581.8Semi standard non polar33892256
Mulberranol,3TMS,isomer #4CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O)=C2C1=O3623.5Semi standard non polar33892256
Mulberranol,4TMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C)C=C2O[Si](C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C)O3)C(O[Si](C)(C)C)=C2C1=O3617.3Semi standard non polar33892256
Mulberranol,1TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O3916.4Semi standard non polar33892256
Mulberranol,1TBDMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O)=C2C1=O3994.4Semi standard non polar33892256
Mulberranol,1TBDMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O)=C2C1=O3881.1Semi standard non polar33892256
Mulberranol,1TBDMS,isomer #4CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O)O3)C(O)=C2C1=O3923.3Semi standard non polar33892256
Mulberranol,2TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4058.0Semi standard non polar33892256
Mulberranol,2TBDMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4015.2Semi standard non polar33892256
Mulberranol,2TBDMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4121.3Semi standard non polar33892256
Mulberranol,2TBDMS,isomer #4CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O)=C2C1=O4146.6Semi standard non polar33892256
Mulberranol,2TBDMS,isomer #5CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O)=C2C1=O4091.6Semi standard non polar33892256
Mulberranol,2TBDMS,isomer #6CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O)=C2C1=O4069.1Semi standard non polar33892256
Mulberranol,3TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4196.9Semi standard non polar33892256
Mulberranol,3TBDMS,isomer #2CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4247.2Semi standard non polar33892256
Mulberranol,3TBDMS,isomer #3CC(C)=CCC1=C(C2=CC=C(O)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4196.5Semi standard non polar33892256
Mulberranol,3TBDMS,isomer #4CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O)=C2C1=O4271.1Semi standard non polar33892256
Mulberranol,4TBDMS,isomer #1CC(C)=CCC1=C(C2=CC=C(O[Si](C)(C)C(C)(C)C)C=C2O[Si](C)(C)C(C)(C)C)OC2=CC3=C(CC(C(C)(C)O[Si](C)(C)C(C)(C)C)O3)C(O[Si](C)(C)C(C)(C)C)=C2C1=O4376.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Mulberranol GC-MS (Non-derivatized) - 70eV, Positivesplash10-0a4i-9024400000-0c04bc1bc95b63aefa112017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mulberranol GC-MS (3 TMS) - 70eV, Positivesplash10-0a4i-9000035000-e150c033ad6273e3ee162017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mulberranol GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Mulberranol 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 - Mulberranol 10V, Positive-QTOFsplash10-0079-0005900000-691495f9d31708ecc0092016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 20V, Positive-QTOFsplash10-01bi-4009700000-9d442b40b2b59b153a2f2016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 40V, Positive-QTOFsplash10-052b-2269000000-0a20559d90268e997e892016-08-02Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 10V, Negative-QTOFsplash10-000i-0000900000-e24bb152f31b627cb0bd2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 20V, Negative-QTOFsplash10-00kr-0014900000-5d8f9e40ed6100a3be292016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 40V, Negative-QTOFsplash10-0a4i-0936100000-db6807942309b8feba2f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 10V, Positive-QTOFsplash10-000i-0000900000-b5f2afccea7aeee35d792021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 20V, Positive-QTOFsplash10-000i-0000900000-b5f2afccea7aeee35d792021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 40V, Positive-QTOFsplash10-000i-0090400000-6dd3ac304fdc2a33408d2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 10V, Negative-QTOFsplash10-000i-0000900000-c34e42b820ea6128d4112021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 20V, Negative-QTOFsplash10-000i-0000900000-c34e42b820ea6128d4112021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Mulberranol 40V, Negative-QTOFsplash10-000f-0190100000-9c94344a7f6b5010d8252021-09-24Wishart 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 IDFDB002737
KNApSAcK IDC00057475
Chemspider ID35013265
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound71438979
PDB IDNot Available
ChEBI ID175532
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1822821
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.. .

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
Mulberranol → 3,4,5-trihydroxy-6-{3-hydroxy-4-[4-hydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-5-oxo-2H,3H,5H-furo[3,2-g]chromen-7-yl]phenoxy}oxane-2-carboxylic aciddetails
Mulberranol → 3,4,5-trihydroxy-6-{5-hydroxy-2-[4-hydroxy-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-5-oxo-2H,3H,5H-furo[3,2-g]chromen-7-yl]phenoxy}oxane-2-carboxylic aciddetails
Mulberranol → 6-{[7-(2,4-dihydroxyphenyl)-2-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-en-1-yl)-5-oxo-2H,3H,5H-furo[3,2-g]chromen-4-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic aciddetails