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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 22:38:41 UTC
Update Date2022-03-07 02:55:18 UTC
HMDB IDHMDB0037400
Secondary Accession Numbers
  • HMDB37400
Metabolite Identification
Common Name(+)-Catechin 6-C-glucoside
Description(+)-Catechin 6-C-glucoside belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone (+)-Catechin 6-C-glucoside has been detected, but not quantified in, green vegetables. This could make (+)-catechin 6-C-glucoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on (+)-Catechin 6-C-glucoside.
Structure
Data?1563863024
Synonyms
ValueSource
6-C-GlucopyranosylcatechinHMDB
6-Glucopyranosyl-(+)-catechinHMDB
6-Glucosyl-(+)-catechinHMDB
Chemical FormulaC21H24O11
Average Molecular Weight452.4087
Monoisotopic Molecular Weight452.13186161
IUPAC Name2-(3,4-dihydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol
Traditional Name2-(3,4-dihydroxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-3,5,7-triol
CAS Registry Number105371-27-5
SMILES
OCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(C(O)C2)C2=CC(O)=C(O)C=C2)C=C1O
InChI Identifier
InChI=1S/C21H24O11/c22-6-14-17(28)18(29)19(30)21(32-14)15-11(25)5-13-8(16(15)27)4-12(26)20(31-13)7-1-2-9(23)10(24)3-7/h1-3,5,12,14,17-30H,4,6H2
InChI KeyPWMSPKVTJLJDDS-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid c-glycosides. Flavonoid C-glycosides are compounds containing a carbohydrate moiety which is C-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid C-glycosides
Alternative Parents
Substituents
  • Catechin
  • Flavonoid c-glycoside
  • 3'-hydroxyflavonoid
  • 3-hydroxyflavonoid
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavan-3-ol
  • Hydroxyflavonoid
  • Flavan
  • Phenolic glycoside
  • Hexose monosaccharide
  • C-glycosyl compound
  • Glycosyl compound
  • Chromane
  • Benzopyran
  • 1-benzopyran
  • Catechol
  • Phenol
  • Alkyl aryl ether
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Monosaccharide
  • Oxane
  • Monocyclic benzene moiety
  • Benzenoid
  • Secondary alcohol
  • Polyol
  • Oxacycle
  • Ether
  • Dialkyl ether
  • Organoheterocyclic compound
  • Alcohol
  • Organic oxygen compound
  • Primary alcohol
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility3.77 g/LALOGPS
logP-0.64ALOGPS
logP-0.96ChemAxon
logS-2.1ALOGPS
pKa (Strongest Acidic)8.78ChemAxon
pKa (Strongest Basic)-3.3ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area200.53 ŲChemAxon
Rotatable Bond Count3ChemAxon
Refractivity107.12 m³·mol⁻¹ChemAxon
Polarizability44.1 ųChemAxon
Number of Rings4ChemAxon
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]+204.73331661259
DarkChem[M-H]-198.02131661259
DeepCCS[M+H]+196.51330932474
DeepCCS[M-H]-194.11830932474
DeepCCS[M-2H]-227.03630932474
DeepCCS[M+Na]+202.42630932474
AllCCS[M+H]+209.032859911
AllCCS[M+H-H2O]+206.632859911
AllCCS[M+NH4]+211.232859911
AllCCS[M+Na]+211.932859911
AllCCS[M-H]-205.632859911
AllCCS[M+Na-2H]-206.532859911
AllCCS[M+HCOO]-207.832859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
(+)-Catechin 6-C-glucosideOCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(C(O)C2)C2=CC(O)=C(O)C=C2)C=C1O4798.7Standard polar33892256
(+)-Catechin 6-C-glucosideOCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(C(O)C2)C2=CC(O)=C(O)C=C2)C=C1O4123.4Standard non polar33892256
(+)-Catechin 6-C-glucosideOCC1OC(C(O)C(O)C1O)C1=C(O)C2=C(OC(C(O)C2)C2=CC(O)=C(O)C=C2)C=C1O4472.4Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
(+)-Catechin 6-C-glucoside,1TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4369.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #2C[Si](C)(C)OC1C(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)OC(CO)C(O)C1O4401.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #3C[Si](C)(C)OC1C(O)C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C1O4431.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #4C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C1O4422.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #5C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O4356.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #6C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14378.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #7C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)=CC=C1O4415.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #8C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O4438.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TMS,isomer #9C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O4403.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4336.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #10C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4305.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #11C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14352.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #12C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4374.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #13C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4342.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #14C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C1O4347.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #15C[Si](C)(C)OC1C(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)OC(CO)C(O)C1O[Si](C)(C)C4370.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #16C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C1O[Si](C)(C)C4373.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #17C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4348.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #18C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4306.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #19C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14362.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4305.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O4374.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #21C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4337.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #22C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4355.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #23C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4308.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #24C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14346.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O4390.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #26C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O)=CC=C1O4356.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #27C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O4344.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4369.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #29C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4340.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4341.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #30C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O4320.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #31C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O4359.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4401.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #33C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4376.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #34C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)=CC=C1O4359.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #35C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4381.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #36C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O4390.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4373.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4344.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4345.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4351.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4355.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TMS,isomer #9C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4347.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4216.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4167.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4182.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4175.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4190.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4267.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4239.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4238.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4234.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4242.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4257.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4234.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4228.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4215.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4250.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4191.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4178.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4214.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4239.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4247.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4255.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #29C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4215.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4217.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #30C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4208.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #31C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4217.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #32C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4236.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4215.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #34C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4179.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #35C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4181.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #36C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4183.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #37C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O4184.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #38C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4150.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #39C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4186.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4186.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #40C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14234.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #41C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14254.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #42C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O4263.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #43C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4238.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #44C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4221.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #45C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4232.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #46C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C4266.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #47C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4180.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #48C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4195.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #49C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4287.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4207.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #50C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4231.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #51C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4180.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #52C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14254.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #53C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O4237.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #54C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4198.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #55C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4181.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #56C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4219.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #57C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O4196.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #58C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4158.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #59C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4158.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4194.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #60C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4121.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #61C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4173.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #62C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4237.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #63C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4215.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #64C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4241.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #65C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4213.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #66C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4233.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #67C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O4222.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #68C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O)=CC=C1O4185.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #69C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4186.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4219.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #70C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4153.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #71C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4182.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #72C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4258.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #73C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4234.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #74C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4271.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #75C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O4240.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #76C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4238.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #77C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4205.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #78C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O4230.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #79C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C4245.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4189.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #80C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O4207.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #81C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4275.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #82C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4247.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #83C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4311.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #84C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4278.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4198.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4084.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4091.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #100C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4075.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #101C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4125.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #102C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4040.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #103C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4047.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #104C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4020.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #105C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4038.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #106C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4011.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #107C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4092.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #108C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O4011.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #109C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C4071.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4115.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #110C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3989.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #111C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4120.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #112C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4074.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #113C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4068.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #114C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4034.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #115C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4065.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #116C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4040.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #117C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4122.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #118C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O4031.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #119C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C4098.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4119.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #120C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O4010.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #121C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4149.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #122C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O4091.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #123C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O4061.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #124C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C4154.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #125C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4141.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #126C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4174.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4064.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4052.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4073.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4037.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4025.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4044.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4104.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4074.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4121.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4117.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4044.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4022.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4069.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4052.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4071.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4101.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4039.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4031.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O4042.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4053.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4011.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4000.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4025.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4073.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4096.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #36C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4086.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #37C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4148.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #38C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4102.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #39C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4073.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4084.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #40C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4100.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #41C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4082.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #42C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4051.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #43C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4084.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #44C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4149.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #45C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4164.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #46C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4153.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #47C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4127.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #48C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O4106.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #49C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4129.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4040.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #50C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4091.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #51C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4104.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #52C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4098.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #53C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4068.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #54C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4079.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #55C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4078.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #56C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4187.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #57C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4073.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #58C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4063.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #59C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4084.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4079.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #60C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O4063.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #61C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4032.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #62C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4141.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #63C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4123.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #64C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4054.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #65C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4021.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #66C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4121.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #67C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4052.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #68C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4021.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #69C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O4079.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4085.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #70C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4054.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #71C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C4121.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #72C[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4105.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #73C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O4035.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #74C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4001.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #75C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4079.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #76C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O4028.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #77C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4000.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #78C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4076.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #79C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O4040.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O4054.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #80C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C4094.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #81C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O4018.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #82C[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14177.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #83C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O4101.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #84C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4083.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #85C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O4103.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #86C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4085.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #87C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4160.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #88C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O4117.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #89C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C4133.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4117.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #90C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C4129.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #91C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O4093.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #92C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4057.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #93C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4114.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #94C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O4055.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #95C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4027.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #96C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O4029.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #97C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O4002.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #98C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4072.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,4TMS,isomer #99C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O4091.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O3900.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3898.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #100C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3959.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #101C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O4014.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #102C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O4002.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #103C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4038.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #104C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4035.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #105C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C4054.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #106C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3922.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #107C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O3926.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #108C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O3902.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #109C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O3942.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3910.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #110C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O3924.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #111C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C4000.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #112C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3889.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #113C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3961.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #114C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3876.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #115C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4024.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #116C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3906.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #117C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3886.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #118C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3985.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #119C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3979.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3901.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #120C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3946.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #121C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3898.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #122C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3877.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #123C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3995.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #124C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3997.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #125C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3952.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #126C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4005.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3942.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3966.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3955.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O3986.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O3925.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O3931.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C3929.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O3877.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O3905.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O3912.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C3909.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4009.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4028.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4020.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O3986.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O3986.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C3992.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3941.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3938.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3957.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3961.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3920.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3934.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3939.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4053.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #36C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O3957.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #37C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3888.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #38C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3888.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #39C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3889.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3904.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #40C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3873.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #41C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3869.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #42C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3872.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #43C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3965.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #44C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3986.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #45C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3979.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #46C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3967.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #47C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3959.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #48C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3967.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #49C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3920.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3935.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #50C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3936.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #51C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3939.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #52C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3895.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #53C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3911.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #54C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3916.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #55C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4027.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #56C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O4027.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #57C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O3999.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #58C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C4018.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #59C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3982.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O3990.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #60C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3997.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #61C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3994.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #62C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3965.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #63C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3979.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #64C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3978.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #65C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4117.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #66C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4023.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #67C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4041.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #68C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4033.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #69C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4040.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3922.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #70C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4021.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #71C[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3969.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #72C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3924.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #73C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O3931.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #74C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O3906.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #75C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3919.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #76C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O3925.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #77C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O3900.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #78C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3908.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #79C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3889.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3934.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #80C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3996.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #81C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4051.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #82C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O3974.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #83C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)=CC=C1O3956.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #84C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O3933.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #85C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O3914.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #86C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C4000.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #87C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O3934.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #88C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O3914.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #89C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C3990.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3926.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #90C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C4003.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #91C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O3943.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #92C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O3922.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #93C[Si](C)(C)OC1=C2CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3998.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #94C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3883.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #95C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3966.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #96C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3867.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #97C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3887.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #98C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3957.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,5TMS,isomer #99C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3873.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O3870.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3841.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3896.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3893.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3893.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3830.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3850.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3832.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3810.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3826.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3811.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3810.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3904.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O3897.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O3901.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C3894.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3854.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3870.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3863.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3837.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3851.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3844.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3809.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3962.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3909.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3929.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3918.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3901.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3885.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #36C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3863.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #37C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3859.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #38C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3858.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #39C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3818.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3805.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #40C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3833.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #41C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3826.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #42C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3804.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #43C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3819.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #44C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3813.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #45C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3936.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #46C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3885.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #47C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3905.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #48C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3893.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #49C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3887.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3793.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #50C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3868.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #51C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3951.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #52C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3961.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #53C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3952.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #54C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3950.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #55C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3934.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #56C[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3994.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #57C[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3854.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #58C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O3838.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #59C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)=CC=C1O3816.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3789.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #60C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3797.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #61C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3779.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #62C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3892.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #63C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3791.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #64C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3775.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #65C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3877.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #66C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3880.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #67C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O3879.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #68C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)=CC=C1O3866.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #69C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C3941.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3785.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #70C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3917.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #71C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3910.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #72C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3835.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #73C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3906.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #74C[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3822.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #75C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3868.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #76C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3865.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #77C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3981.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #78C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O3792.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #79C[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)=CC=C1O3773.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3831.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #80C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C3876.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #81C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3914.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #82C[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3865.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #83C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3863.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #84C[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3CC2O[Si](C)(C)C)C=C1O[Si](C)(C)C3866.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,6TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C)CC3=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3848.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4602.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1C(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)OC(CO)C(O)C1O4668.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C1O4692.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C1O4677.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O4617.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14636.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)=CC=C1O4649.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O4667.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,1TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O4623.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4798.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4797.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14851.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)C=C1O4857.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)=CC=C1O4821.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C1O4829.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1C(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C4839.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C1O[Si](C)(C)C(C)(C)C4829.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4811.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4790.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14844.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4795.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)C=C1O4855.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4818.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4808.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4787.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14827.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O4856.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O)=CC=C1O4819.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O4833.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)C=C1O4844.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)=CC=C1O4814.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O)C(O)C1O4825.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=C2CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O4818.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O4839.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O4874.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)=CC=C1O4851.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)=CC=C1O4823.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C(C)(C)C4849.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O4851.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4835.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4808.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4818.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4810.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4809.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4818.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4903.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4872.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4868.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4868.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4858.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O)C(O)C1O4950.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O)C(O)C1O4920.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4907.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4894.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4881.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4947.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O)C(O)C(O)C1O4911.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4926.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4925.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4921.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4884.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4881.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4878.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4899.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4910.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4894.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4911.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O4945.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4885.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4879.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4903.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)C=C1O4933.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)=CC=C1O4895.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4858.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4853.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)C=C1O4908.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)=CC=C1O4868.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=C2CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4871.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C4)C(O)CC3=C2O)C(O)C(O)C1O4906.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14885.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)=C2O)OC1C1=CC=C(O)C(O)=C14886.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O4935.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)=CC=C1O4904.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)C=C1O4914.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)C=C1O4917.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)C=C1O[Si](C)(C)C(C)(C)C4957.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)=CC=C1O4869.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C(O)=C3CC2O)=CC=C1O4872.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4896.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4892.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4871.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=C2CC(O)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4839.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1CC2=C(C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)OC1C1=CC=C(O)C(O)=C14863.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)C=C1O4900.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4855.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4895.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4884.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #57CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)C=C1O4927.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #58CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)=CC=C1O4887.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #59CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)C=C1O4889.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4895.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #60CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)=CC=C1O4847.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #61CC(C)(C)[Si](C)(C)OC1=C2CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4862.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #62CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O4913.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #63CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)=CC=C1O4879.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #64CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C(C)(C)C4937.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #65CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4897.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #66CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4884.4Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #67CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O4924.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #68CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O)=CC=C1O4884.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #69CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)C=C1O4893.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C3OC(C4=CC=C(O)C(O)=C4)C(O)CC3=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4884.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #70CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)=CC=C1O4851.2Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #71CC(C)(C)[Si](C)(C)OC1=C2CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)OC2=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4854.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #72CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O4905.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #73CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)=CC=C1O4873.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #74CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C(C)(C)C4938.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #75CC(C)(C)[Si](C)(C)OC1=CC2=C(CC(O[Si](C)(C)C(C)(C)C)C(C3=CC=C(O)C(O)=C3)O2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O4939.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #76CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)C=C1O4970.6Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #77CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)=CC=C1O4933.9Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #78CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O4951.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #79CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O)C=C1O[Si](C)(C)C(C)(C)C4968.5Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O)C(O)=C4)C(O[Si](C)(C)C(C)(C)C)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4881.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #80CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3CC2O[Si](C)(C)C(C)(C)C)=CC=C1O4921.7Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #81CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O4961.3Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #82CC(C)(C)[Si](C)(C)OC1=CC(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)=CC=C1O4936.0Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #83CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4999.8Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #84CC(C)(C)[Si](C)(C)OC1=CC=C(C2OC3=CC(O[Si](C)(C)C(C)(C)C)=C(C4OC(CO)C(O)C(O)C4O)C(O)=C3CC2O)C=C1O[Si](C)(C)C(C)(C)C4983.1Semi standard non polar33892256
(+)-Catechin 6-C-glucoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C3OC(C4=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C4)C(O)CC3=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4917.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-0uk9-3109300000-2e3407a578c7bf35984e2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (3 TMS) - 70eV, Positivesplash10-0udi-1400549000-3d3bc28c449b945d76382017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_4_58) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_5_71) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_5_75) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_5_76) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_5_77) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_6_57) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_6_58) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_6_59) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_6_63) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_6_64) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (TMS_6_65) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - (+)-Catechin 6-C-glucoside GC-MS ("(+)-Catechin 6-C-glucoside,4TMS,#58" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 10V, Positive-QTOFsplash10-0udr-0142900000-8d746a1077f9cb353c7f2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 20V, Positive-QTOFsplash10-0uei-2896700000-7d8b17efd0cd408493ba2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 40V, Positive-QTOFsplash10-0f6t-1921100000-0d2a91cf683d65477be02015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 10V, Negative-QTOFsplash10-0udi-0112900000-191af36c2ca65cdd52642015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 20V, Negative-QTOFsplash10-0udi-4934400000-183477aeb3f38fb5cd642015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 40V, Negative-QTOFsplash10-0k95-3920000000-880ca4f155bea3cfedd82015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 10V, Positive-QTOFsplash10-0udi-0002900000-520bdc127b419776a0442021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 20V, Positive-QTOFsplash10-0udi-1219500000-e9fb481224d29fd7a32f2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 40V, Positive-QTOFsplash10-01b9-6609100000-3bab37e91c81a8ca3a122021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 10V, Negative-QTOFsplash10-0udi-0002900000-b5be6cf8091c968383b12021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 20V, Negative-QTOFsplash10-0159-1009800000-f92ed7f3a23d6fcd8b7f2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - (+)-Catechin 6-C-glucoside 40V, Negative-QTOFsplash10-05mo-9468400000-e676410522a8a6675b272021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart 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 IDFDB016444
KNApSAcK IDC00006358
Chemspider ID35014410
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound59010767
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
(+)-Catechin 6-C-glucoside → 2-(4-hydroxy-3-methoxyphenyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-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
(+)-Catechin 6-C-glucoside → ({6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-yl]-3,4,5-trihydroxyoxan-2-yl}methoxy)sulfonic aciddetails
(+)-Catechin 6-C-glucoside → {6-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-yl]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl}oxidanesulfonic aciddetails
(+)-Catechin 6-C-glucoside → {2-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-yl]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl}oxidanesulfonic aciddetails
(+)-Catechin 6-C-glucoside → {2-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-1-benzopyran-6-yl]-4,5-dihydroxy-6-(hydroxymethyl)oxan-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
(+)-Catechin 6-C-glucoside → 3,4,5-trihydroxy-6-(2-hydroxy-5-{3,5,7-trihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-2-yl}phenoxy)oxane-2-carboxylic aciddetails
(+)-Catechin 6-C-glucoside → 6-{[2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-7-yl]oxy}-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
(+)-Catechin 6-C-glucoside → (2-hydroxy-5-{3,5,7-trihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4-dihydro-2H-1-benzopyran-2-yl}phenyl)oxidanesulfonic aciddetails