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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:47:11 UTC
Update Date2022-03-07 02:53:12 UTC
HMDB IDHMDB0032007
Secondary Accession Numbers
  • HMDB32007
Metabolite Identification
Common NameEpifisetinidol-(4beta->8)-catechin
DescriptionEpifisetinidol-(4beta->8)-catechin belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''. Based on a literature review very few articles have been published on Epifisetinidol-(4beta->8)-catechin.
Structure
Data?1563862206
Synonyms
ValueSource
Epifisetinidol-(4b->8)-catechinGenerator
Epifisetinidol-(4β->8)-catechinGenerator
Epifisetinidol(4b->8)catechinHMDB
Chemical FormulaC30H26O11
Average Molecular Weight562.5208
Monoisotopic Molecular Weight562.147511674
IUPAC Name2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol
Traditional Name2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol
CAS Registry NumberNot Available
SMILES
OC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=C1C=CC(O)=C3)C1=CC(O)=C(O)C=C1)=C(O)C=C2O
InChI Identifier
InChI=1S/C30H26O11/c31-14-3-4-15-24(9-14)40-29(13-2-6-18(33)21(36)8-13)27(39)25(15)26-22(37)11-19(34)16-10-23(38)28(41-30(16)26)12-1-5-17(32)20(35)7-12/h1-9,11,23,25,27-29,31-39H,10H2
InChI KeyCVPALQKJIJFGCD-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as biflavonoids and polyflavonoids. These are organic compounds containing at least two flavan/flavone units. These units are usually linked through CC or C-O-C bonds. Some examples include C2-O-C3, C2-O-C4, C3'-C3''', and C6-C8''.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassBiflavonoids and polyflavonoids
Direct ParentBiflavonoids and polyflavonoids
Alternative Parents
Substituents
  • B-type proanthocyanidin
  • Bi- and polyflavonoid skeleton
  • Proanthocyanidin
  • Catechin
  • Flavan-3-ol
  • Hydroxyflavonoid
  • 3'-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 3-hydroxyflavonoid
  • Flavan
  • Chromane
  • 1-benzopyran
  • Benzopyran
  • Catechol
  • Phenol
  • 1-hydroxy-2-unsubstituted benzenoid
  • Alkyl aryl ether
  • 1-hydroxy-4-unsubstituted benzenoid
  • Benzenoid
  • Monocyclic benzene moiety
  • Secondary alcohol
  • Polyol
  • Organoheterocyclic compound
  • Oxacycle
  • Ether
  • Hydrocarbon derivative
  • Alcohol
  • Organic oxygen compound
  • Organooxygen compound
  • 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 SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.078 g/LALOGPS
logP2.4ALOGPS
logP3.42ChemAxon
logS-3.9ALOGPS
pKa (Strongest Acidic)8.73ChemAxon
pKa (Strongest Basic)-3.4ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area200.53 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity144.53 m³·mol⁻¹ChemAxon
Polarizability56.35 ųChemAxon
Number of Rings6ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+227.99331661259
DarkChem[M-H]-219.82131661259
DeepCCS[M+H]+216.73430932474
DeepCCS[M-H]-214.59130932474
DeepCCS[M-2H]-247.83130932474
DeepCCS[M+Na]+222.64330932474
AllCCS[M+H]+234.932859911
AllCCS[M+H-H2O]+233.232859911
AllCCS[M+NH4]+236.532859911
AllCCS[M+Na]+236.932859911
AllCCS[M-H]-228.432859911
AllCCS[M+Na-2H]-229.832859911
AllCCS[M+HCOO]-231.632859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Epifisetinidol-(4beta->8)-catechinOC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=C1C=CC(O)=C3)C1=CC(O)=C(O)C=C1)=C(O)C=C2O7039.1Standard polar33892256
Epifisetinidol-(4beta->8)-catechinOC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=C1C=CC(O)=C3)C1=CC(O)=C(O)C=C1)=C(O)C=C2O4963.4Standard non polar33892256
Epifisetinidol-(4beta->8)-catechinOC1CC2=C(OC1C1=CC(O)=C(O)C=C1)C(C1C(O)C(OC3=C1C=CC(O)=C3)C1=CC(O)=C(O)C=C1)=C(O)C=C2O5871.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #1C[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=CC=C(O)C=C4OC(C4=CC=C(O)C(O)=C4)C3O)=C2OC1C1=CC=C(O)C(O)=C15523.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #2C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5586.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #3C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5600.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #4C[Si](C)(C)OC1C(C2=CC=C(O)C(O)=C2)OC2=CC(O)=CC=C2C1C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25534.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #5C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25590.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #6C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O5602.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #7C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O5614.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #8C[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O5578.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O25570.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #1C[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O25464.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #10C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5494.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #11C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25480.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #12C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5529.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #13C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5506.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #14C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5458.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #15C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5488.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #16C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5517.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5516.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #18C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25508.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #19C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5543.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #2C[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O5466.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5526.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5483.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #22C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5489.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #23C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC=C1O5473.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #24C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25454.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #25C[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O[Si](C)(C)C5466.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #26C[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O25456.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #27C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25506.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #28C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25482.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #29C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25473.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #3C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25471.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #30C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25479.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #31C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O5506.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #32C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O5507.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O[Si](C)(C)C5502.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O5526.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #35C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O5528.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #36C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O25470.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5504.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #5C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC=C1O5487.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #6C[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=CC=C(O)C=C4OC(C4=CC=C(O)C(O)=C4)C3O[Si](C)(C)C)=C2OC1C1=CC=C(O)C(O)=C15435.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #7C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5491.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #8C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5482.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TMS,isomer #9C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5494.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #1C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O25368.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #10C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC=C1O5390.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #11C[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O[Si](C)(C)C5354.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #12C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5406.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #13C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5390.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #14C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25396.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #15C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25373.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #16C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25346.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #17C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C25396.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #18C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25379.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #19C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5423.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #2C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25378.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5403.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)C=C1O5389.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #22C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O[Si](C)(C)C5431.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #23C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5395.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #24C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5371.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #25C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC=C1O5370.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5385.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #27C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5367.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5430.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #29C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5327.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #3C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5412.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #30C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25338.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5335.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #32C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5308.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #33C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5347.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5415.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #35C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25320.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #36C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5334.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #37C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5307.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #38C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5344.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #39C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5409.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #4C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC=C1O5393.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #40C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25311.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #41C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25292.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #42C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25326.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #43C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C25398.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #44C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5406.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #45C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5352.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #46C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5377.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #47C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O5324.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #48C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)=CC=C1O5377.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #49C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5391.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #5C[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O25357.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #50C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5349.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #51C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25356.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #52C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5355.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #53C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5334.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #54C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5372.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #55C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25341.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #56C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5355.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #57C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5333.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #58C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5371.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #59C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25332.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #6C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5405.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #60C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25313.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #61C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25354.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #62C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O5408.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #63C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O5381.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #64C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O5361.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #65C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25352.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #66C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5374.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #67C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5376.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #68C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5408.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #69C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25333.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #7C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5392.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #70C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC=C1O5357.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #71C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC=C1O5361.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #72C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25340.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #73C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25347.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #74C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O25341.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #75C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25402.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #76C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25338.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #77C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25355.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #78C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25319.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #79C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25339.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #8C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25374.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #80C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25345.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #81C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O5334.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #82C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O[Si](C)(C)C5417.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #83C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O[Si](C)(C)C5424.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #84C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O5352.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,3TMS,isomer #9C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5412.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #1C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25216.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #10C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C25214.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #100C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O5142.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #101C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O5122.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #102C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25127.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #103C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25105.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #104C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25156.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #105C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O5194.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #106C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O5128.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #107C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O5113.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #108C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25193.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #109C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25123.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #11C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25204.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #110C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25107.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #111C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O5231.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #112C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25251.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #113C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25155.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #114C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25158.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #115C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5155.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #116C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5262.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #117C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5259.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #118C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25141.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #119C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25146.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #12C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5191.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #120C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C)=CC=C1O5140.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #121C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25172.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #122C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25225.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #123C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25237.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #124C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25132.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #125C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25110.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #126C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O[Si](C)(C)C5225.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #13C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5184.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #14C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)C=C1O5227.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #15C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O[Si](C)(C)C5297.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #16C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5169.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #17C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5150.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #18C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC=C1O5208.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #19C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5221.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #2C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5211.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #20C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5202.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5293.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #22C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25207.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #23C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25188.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #24C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25218.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #25C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C25204.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #26C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25191.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5176.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5171.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #29C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)C=C1O5237.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #3C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)=CC=C1O5192.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #30C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O[Si](C)(C)C5304.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5156.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #32C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5139.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #33C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)=CC=C1O5218.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5232.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #35C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5213.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #36C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5297.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #37C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25293.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #38C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25220.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #39C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C25170.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #4C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C2=C1CC(O[Si](C)(C)C)C(C1=CC=C(O)C(O)=C1)O25204.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #40C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25160.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #41C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25201.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #42C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C25154.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #43C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25141.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #44C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C25221.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #45C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25205.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #46C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C25298.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #47C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O5277.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #48C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O[Si](C)(C)C)C=C1O5210.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #49C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C4)C2O)C=C1O5286.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #5C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5200.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #50C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)C=C1O5197.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #51C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5258.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #52C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C)C4)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5299.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #53C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)C=C1O5192.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #54C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O[Si](C)(C)C)C4)C2O)=CC=C1O5262.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #55C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O5172.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #56C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5292.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #57C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25109.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #58C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5098.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #59C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5065.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #6C[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5187.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #60C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)=CC=C1O5126.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #61C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C5214.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #62C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25123.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #63C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25104.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #64C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25139.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #65C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C25234.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #66C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5211.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #67C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5119.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #68C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5177.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #69C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O5088.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #7C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25217.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #70C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)=CC=C1O5186.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #71C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5242.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #72C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25107.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #73C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25083.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #74C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25134.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #75C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C25221.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #76C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)C=C1O5197.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #77C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5111.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #78C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)=CC=C1O5166.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #79C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O5083.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #8C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25198.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #80C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O)=CC=C1O5175.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #81C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O[Si](C)(C)C5250.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #82C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25174.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #83C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25101.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #84C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C25189.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #85C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C25083.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #86C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C25173.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #87C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C1)C(O)C25247.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #88C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O[Si](C)(C)C)C=C1O5224.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #89C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O[Si](C)(C)C5271.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #9C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C25214.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #90C[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O[Si](C)(C)C)=CC=C1O5200.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #91C[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C(O)C4)C2O[Si](C)(C)C)=CC=C1O5202.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #92C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25132.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #93C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O)=C3)C2O)C=C1O5107.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #94C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C)=C3)C2O)C=C1O5089.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #95C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C)C=C1O5151.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #96C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25143.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #97C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25125.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #98C[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C)C2C1=C(O)C=C(O[Si](C)(C)C)C2=C1OC(C1=CC=C(O[Si](C)(C)C)C(O)=C1)C(O)C25161.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,4TMS,isomer #99C[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)C2O)C=C1O5206.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=CC=C(O)C=C4OC(C4=CC=C(O)C(O)=C4)C3O)=C2OC1C1=CC=C(O)C(O)=C15778.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O5841.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O5844.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1C(C2=CC=C(O)C(O)=C2)OC2=CC(O)=CC=C2C1C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25792.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C25821.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O5857.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O5858.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O5829.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,1TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O25818.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O[Si](C)(C)C(C)(C)C)C(C1=CC=C(O)C(O)=C1)O26028.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O6065.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C26043.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)C(O)C4)C2O)C=C1O6080.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)C2O)=CC=C1O6058.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)=CC=C1O6027.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O[Si](C)(C)C(C)(C)C6051.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O6074.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O6079.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(O)C26061.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)C2O)C=C1O6089.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O6025.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)C2O)C=C1O6076.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)C=C1O6045.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C(C)(C)C)C=C1O6047.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O[Si](C)(C)C(C)(C)C)=CC=C1O6038.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C(C)(C)C)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C26006.4Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(O)=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=C1C1C2=CC=C(O)C=C2OC(C2=CC=C(O)C(O)=C2)C1O[Si](C)(C)C(C)(C)C6017.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O[Si](C)(C)C(C)(C)C)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O26012.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C26061.3Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C26044.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O[Si](C)(C)C(C)(C)C)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C26033.1Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O[Si](C)(C)C(C)(C)C)C26027.2Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC=C2C(=C1)OC(C1=CC=C(O)C(O)=C1)C(O)C2C1=C(O)C=C(O[Si](C)(C)C(C)(C)C)C2=C1OC(C1=CC=C(O)C(O)=C1)C(O)C26037.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O6071.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)=CC=C1O6067.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O[Si](C)(C)C(C)(C)C6058.5Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O6086.0Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O)C4)C2O)C=C1O6081.9Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C2=C1CC(O)C(C1=CC=C(O)C(O)=C1)O26030.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C(C)(C)C)C4)C2O)C=C1O6069.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=CC=C3C(C3=C(O)C=C(O)C4=C3OC(C3=CC=C(O)C(O)=C3)C(O[Si](C)(C)C(C)(C)C)C4)C2O)=CC=C1O6062.6Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1CC2=C(O)C=C(O)C(C3C4=CC=C(O)C=C4OC(C4=CC=C(O)C(O)=C4)C3O[Si](C)(C)C(C)(C)C)=C2OC1C1=CC=C(O)C(O)=C15973.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=C(CC2O[Si](C)(C)C(C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)C=C1O6060.8Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O[Si](C)(C)C(C)(C)C)C(O)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O6059.7Semi standard non polar33892256
Epifisetinidol-(4beta->8)-catechin,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=C(CC2O)C(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2C3=CC=C(O)C=C3OC(C3=CC=C(O)C(O)=C3)C2O)=CC=C1O6060.1Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (Non-derivatized) - 70eV, Positivesplash10-00e9-0511690000-e683b288ae7c1acca9b72017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (1 TMS) - 70eV, Positivesplash10-00di-9310213000-22d821ba897e43cb0cd62017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS ("Epifisetinidol-(4beta->8)-catechin,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Epifisetinidol-(4beta->8)-catechin GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 10V, Positive-QTOFsplash10-03di-0115490000-d31ef21658e5ac7b5d2e2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 20V, Positive-QTOFsplash10-000l-0494620000-fcbb8d5f366e8c0e16862015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 40V, Positive-QTOFsplash10-00b9-0491010000-d7b494c812f96ab8af6b2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 10V, Negative-QTOFsplash10-03di-0110190000-87063fb873612c2051772015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 20V, Negative-QTOFsplash10-0f79-0950330000-6ef4e209767d6f7958f22015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 40V, Negative-QTOFsplash10-0a4i-0941000000-9828708dd766d3d570602015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 10V, Negative-QTOFsplash10-03di-0000090000-f37ba1c5470c3a6f63972021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 20V, Negative-QTOFsplash10-0ik9-0000590000-7683b463f235667863d02021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 40V, Negative-QTOFsplash10-00b9-0471940000-e260fc9e088e561a1f342021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 10V, Positive-QTOFsplash10-03di-0000190000-fea0f92c7ca98e5c5b532021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 20V, Positive-QTOFsplash10-03du-0200950000-7e933d138f331f080a922021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Epifisetinidol-(4beta->8)-catechin 40V, Positive-QTOFsplash10-05gi-0901550000-8c369921a0750e7f7ba92021-09-22Wishart 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 IDFDB008705
KNApSAcK IDNot Available
Chemspider ID35013429
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound14332863
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.. .

Enzymes

General function:
Involved in magnesium ion binding
Specific function:
Catalyzes the O-methylation, and thereby the inactivation, of catecholamine neurotransmitters and catechol hormones. Also shortens the biological half-lives of certain neuroactive drugs, like L-DOPA, alpha-methyl DOPA and isoproterenol.
Gene Name:
COMT
Uniprot ID:
P21964
Molecular weight:
30036.77
Reactions
Epifisetinidol-(4beta->8)-catechin → 8-[3,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-trioldetails
Epifisetinidol-(4beta->8)-catechin → 8-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-trioldetails
General function:
Involved in sulfotransferase activity
Specific function:
Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of many hormones, neurotransmitters, drugs and xenobiotic compounds. Sulfonation increases the water solubility of most compounds, and therefore their renal excretion, but it can also result in bioactivation to form active metabolites. Sulfates hydroxysteroids like DHEA. Isoform 1 preferentially sulfonates cholesterol, and isoform 2 avidly sulfonates pregnenolone but not cholesterol.
Gene Name:
SULT2B1
Uniprot ID:
O00204
Molecular weight:
39598.595
Reactions
Epifisetinidol-(4beta->8)-catechin → [2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-7-hydroxy-3,4-dihydro-2H-1-benzopyran-3-yl]oxidanesulfonic aciddetails
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
Epifisetinidol-(4beta->8)-catechin → 6-{[2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-3,5-dihydroxy-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
Epifisetinidol-(4beta->8)-catechin → 6-(4-{4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl}-2-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
Epifisetinidol-(4beta->8)-catechin → 6-(5-{4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl}-2-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
Epifisetinidol-(4beta->8)-catechin → 6-{[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-3-hydroxy-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
Epifisetinidol-(4beta->8)-catechin → 6-(5-{8-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl}-2-hydroxyphenoxy)-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
General function:
sulfotransferase activity
Specific function:
Sulfotransferase that utilizes 3'-phospho-5'-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of phenolic monoamines (neurotransmitters such as dopamine, norepinephrine and serotonin) and phenolic and catechol drugs.
Gene Name:
SULT1A3
Uniprot ID:
P0DMM9
Molecular weight:
34195.96
Reactions
Epifisetinidol-(4beta->8)-catechin → (5-{4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-8-yl]-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl}-2-hydroxyphenyl)oxidanesulfonic aciddetails
Epifisetinidol-(4beta->8)-catechin → (5-{8-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-1-benzopyran-4-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-2-yl}-2-hydroxyphenyl)oxidanesulfonic aciddetails