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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:39:24 UTC
Update Date2022-03-07 02:52:43 UTC
HMDB IDHMDB0030851
Secondary Accession Numbers
  • HMDB30851
Metabolite Identification
Common NameAspalathin
DescriptionAspalathin belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position. Thus, aspalathin is considered to be a flavonoid. Based on a literature review very few articles have been published on Aspalathin.
Structure
Data?1563862047
Synonyms
ValueSource
1-(3-C-b-D-Glucopyranosyl-2,4,6-trihydroxyphenyl)-3-(3,4-dihydroxyphenyl)-1-propanoneHMDB
3'-Glucosyl-2',3,4,4',6'-pentahydroxydihydrochalconeHMDB
3-(3,4-Dihydroxyphenyl)-1-(3-beta-D-glucopyranosyl-2,4,6-trihydroxyphenyl)-1-propanoneHMDB
Chemical FormulaC21H24O11
Average Molecular Weight452.4087
Monoisotopic Molecular Weight452.13186161
IUPAC Name3-(3,4-dihydroxyphenyl)-1-{2,4,6-trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}propan-1-one
Traditional Nameaspalathin
CAS Registry NumberNot Available
SMILES
OCC1OC(C(O)C(O)C1O)C1=C(O)C=C(O)C(C(=O)CCC2=CC(O)=C(O)C=C2)=C1O
InChI Identifier
InChI=1S/C21H24O11/c22-7-14-17(28)19(30)20(31)21(32-14)16-13(27)6-12(26)15(18(16)29)10(24)4-2-8-1-3-9(23)11(25)5-8/h1,3,5-6,14,17,19-23,25-31H,2,4,7H2
InChI KeyVCPUQYKWJRESOC-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as 2'-hydroxy-dihydrochalcones. These are organic compounds containing dihydrochalcone skeleton that carries a hydroxyl group at the 2'-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassLinear 1,3-diarylpropanoids
Sub ClassChalcones and dihydrochalcones
Direct Parent2'-Hydroxy-dihydrochalcones
Alternative Parents
Substituents
  • 2'-hydroxy-dihydrochalcone
  • Phenolic glycoside
  • Cinnamylphenol
  • Alkyl-phenylketone
  • Hexose monosaccharide
  • Glycosyl compound
  • Acylphloroglucinol derivative
  • C-glycosyl compound
  • Butyrophenone
  • Phloroglucinol derivative
  • Phenylketone
  • Benzenetriol
  • Aryl ketone
  • Catechol
  • Aryl alkyl ketone
  • Benzoyl
  • 1-hydroxy-4-unsubstituted benzenoid
  • Phenol
  • 1-hydroxy-2-unsubstituted benzenoid
  • Benzenoid
  • Monosaccharide
  • Monocyclic benzene moiety
  • Oxane
  • Vinylogous acid
  • Ketone
  • Secondary alcohol
  • Oxacycle
  • Organoheterocyclic compound
  • Polyol
  • Dialkyl ether
  • Ether
  • Alcohol
  • Organic oxygen compound
  • Primary alcohol
  • Organic oxide
  • Hydrocarbon derivative
  • Organooxygen compound
  • Aromatic heteromonocyclic compound
Molecular FrameworkAromatic heteromonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility2.49 g/LALOGPS
logP0.03ALOGPS
logP0.83ChemAxon
logS-2.3ALOGPS
pKa (Strongest Acidic)7.57ChemAxon
pKa (Strongest Basic)-3.6ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area208.37 ŲChemAxon
Rotatable Bond Count6ChemAxon
Refractivity108.81 m³·mol⁻¹ChemAxon
Polarizability44.5 ųChemAxon
Number of Rings3ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DarkChem[M+H]+203.8631661259
DarkChem[M-H]-197.64231661259
DeepCCS[M+H]+195.78730932474
DeepCCS[M-H]-193.39130932474
DeepCCS[M-2H]-226.32830932474
DeepCCS[M+Na]+201.69930932474
AllCCS[M+H]+208.632859911
AllCCS[M+H-H2O]+206.232859911
AllCCS[M+NH4]+210.932859911
AllCCS[M+Na]+211.532859911
AllCCS[M-H]-205.032859911
AllCCS[M+Na-2H]-206.132859911
AllCCS[M+HCOO]-207.532859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
AspalathinOCC1OC(C(O)C(O)C1O)C1=C(O)C=C(O)C(C(=O)CCC2=CC(O)=C(O)C=C2)=C1O5050.5Standard polar33892256
AspalathinOCC1OC(C(O)C(O)C1O)C1=C(O)C=C(O)C(C(=O)CCC2=CC(O)=C(O)C=C2)=C1O3818.1Standard non polar33892256
AspalathinOCC1OC(C(O)C(O)C1O)C1=C(O)C=C(O)C(C(=O)CCC2=CC(O)=C(O)C=C2)=C1O4298.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Aspalathin,1TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4170.2Semi standard non polar33892256
Aspalathin,1TMS,isomer #2C[Si](C)(C)OC1C(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)OC(CO)C(O)C1O4186.6Semi standard non polar33892256
Aspalathin,1TMS,isomer #3C[Si](C)(C)OC1C(O)C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C1O4203.6Semi standard non polar33892256
Aspalathin,1TMS,isomer #4C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C1O4189.9Semi standard non polar33892256
Aspalathin,1TMS,isomer #5C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O)C1O4219.9Semi standard non polar33892256
Aspalathin,1TMS,isomer #6C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14235.7Semi standard non polar33892256
Aspalathin,1TMS,isomer #7C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4180.0Semi standard non polar33892256
Aspalathin,1TMS,isomer #8C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4212.7Semi standard non polar33892256
Aspalathin,1TMS,isomer #9C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O)C1O4165.3Semi standard non polar33892256
Aspalathin,2TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4104.9Semi standard non polar33892256
Aspalathin,2TMS,isomer #10C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14157.0Semi standard non polar33892256
Aspalathin,2TMS,isomer #11C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O4041.5Semi standard non polar33892256
Aspalathin,2TMS,isomer #12C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O4019.2Semi standard non polar33892256
Aspalathin,2TMS,isomer #13C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4088.8Semi standard non polar33892256
Aspalathin,2TMS,isomer #14C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C1O4094.3Semi standard non polar33892256
Aspalathin,2TMS,isomer #15C[Si](C)(C)OC1C(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)OC(CO)C(O)C1O[Si](C)(C)C4117.8Semi standard non polar33892256
Aspalathin,2TMS,isomer #16C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C1O[Si](C)(C)C4116.2Semi standard non polar33892256
Aspalathin,2TMS,isomer #17C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4090.2Semi standard non polar33892256
Aspalathin,2TMS,isomer #18C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14145.5Semi standard non polar33892256
Aspalathin,2TMS,isomer #19C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O4029.6Semi standard non polar33892256
Aspalathin,2TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4147.4Semi standard non polar33892256
Aspalathin,2TMS,isomer #20C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O4005.3Semi standard non polar33892256
Aspalathin,2TMS,isomer #21C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O4084.4Semi standard non polar33892256
Aspalathin,2TMS,isomer #22C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4106.0Semi standard non polar33892256
Aspalathin,2TMS,isomer #23C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14153.5Semi standard non polar33892256
Aspalathin,2TMS,isomer #24C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O4037.4Semi standard non polar33892256
Aspalathin,2TMS,isomer #25C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)=CC=C1O4015.1Semi standard non polar33892256
Aspalathin,2TMS,isomer #26C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4094.3Semi standard non polar33892256
Aspalathin,2TMS,isomer #27C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14175.1Semi standard non polar33892256
Aspalathin,2TMS,isomer #28C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4111.3Semi standard non polar33892256
Aspalathin,2TMS,isomer #29C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4080.8Semi standard non polar33892256
Aspalathin,2TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O4060.4Semi standard non polar33892256
Aspalathin,2TMS,isomer #30C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O4149.3Semi standard non polar33892256
Aspalathin,2TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14166.9Semi standard non polar33892256
Aspalathin,2TMS,isomer #32C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4147.7Semi standard non polar33892256
Aspalathin,2TMS,isomer #33C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4125.6Semi standard non polar33892256
Aspalathin,2TMS,isomer #34C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O4076.9Semi standard non polar33892256
Aspalathin,2TMS,isomer #35C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C4075.8Semi standard non polar33892256
Aspalathin,2TMS,isomer #36C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O4092.7Semi standard non polar33892256
Aspalathin,2TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O4038.8Semi standard non polar33892256
Aspalathin,2TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O4089.0Semi standard non polar33892256
Aspalathin,2TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O4087.4Semi standard non polar33892256
Aspalathin,2TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O4078.6Semi standard non polar33892256
Aspalathin,2TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C4094.0Semi standard non polar33892256
Aspalathin,2TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4107.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4045.5Semi standard non polar33892256
Aspalathin,3TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O4063.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O4065.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O4052.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C4067.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3944.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3948.4Semi standard non polar33892256
Aspalathin,3TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3923.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3914.7Semi standard non polar33892256
Aspalathin,3TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3936.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3940.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O3943.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3909.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3896.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3920.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4005.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4003.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4012.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4029.7Semi standard non polar33892256
Aspalathin,3TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4035.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4041.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #29C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14053.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3923.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #30C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O3952.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #31C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3935.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #32C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C4022.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #33C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4014.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #34C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4025.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #35C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14075.7Semi standard non polar33892256
Aspalathin,3TMS,isomer #36C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14090.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #37C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14061.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #38C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O4012.5Semi standard non polar33892256
Aspalathin,3TMS,isomer #39C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3997.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O4018.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #40C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O3922.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #41C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3943.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #42C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3941.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #43C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3959.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #44C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3911.5Semi standard non polar33892256
Aspalathin,3TMS,isomer #45C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3925.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #46C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3933.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #47C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4013.7Semi standard non polar33892256
Aspalathin,3TMS,isomer #48C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4021.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #49C[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4080.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O4010.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #50C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4032.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #51C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14090.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #52C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3953.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #53C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3931.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #54C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4022.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #55C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14024.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #56C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3940.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #57C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3927.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #58C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O3995.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #59C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14050.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3997.4Semi standard non polar33892256
Aspalathin,3TMS,isomer #60C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3984.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #61C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3965.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #62C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3920.3Semi standard non polar33892256
Aspalathin,3TMS,isomer #63C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3928.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #64C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3912.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #65C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14056.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #66C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O3946.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #67C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)=CC=C1O3931.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #68C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O4021.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #69C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14068.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C4019.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #70C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O4005.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #71C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)=CC=C1O3988.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #72C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O3940.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #73C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O[Si](C)(C)C3954.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #74C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O3932.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #75C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14098.0Semi standard non polar33892256
Aspalathin,3TMS,isomer #76C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4040.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #77C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4017.5Semi standard non polar33892256
Aspalathin,3TMS,isomer #78C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O4005.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #79C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C4008.5Semi standard non polar33892256
Aspalathin,3TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O4005.7Semi standard non polar33892256
Aspalathin,3TMS,isomer #80C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O3991.1Semi standard non polar33892256
Aspalathin,3TMS,isomer #81C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O4059.2Semi standard non polar33892256
Aspalathin,3TMS,isomer #82C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O4048.6Semi standard non polar33892256
Aspalathin,3TMS,isomer #83C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C4056.9Semi standard non polar33892256
Aspalathin,3TMS,isomer #84C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4002.8Semi standard non polar33892256
Aspalathin,3TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3990.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O3893.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3860.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #100C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3890.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #101C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3851.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #102C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13953.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #103C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3903.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #104C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3896.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #105C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3879.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #106C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3876.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #107C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3869.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #108C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3900.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #109C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3892.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3845.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #110C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3921.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #111C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3866.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #112C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13983.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #113C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O3907.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #114C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)=CC=C1O3902.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #115C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O3872.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #116C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O[Si](C)(C)C3890.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #117C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O3865.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #118C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O3920.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #119C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O3912.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3834.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #120C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O[Si](C)(C)C3937.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #121C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3889.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #122C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O3965.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #123C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O3951.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #124C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C3969.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #125C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3948.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #126C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C4001.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3830.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3851.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3838.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3941.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3917.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3945.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3950.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3882.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3964.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3965.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3932.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3915.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3904.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3895.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3906.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3905.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3893.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3884.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3973.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3893.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3986.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3972.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3991.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4007.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4023.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #36C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4024.5Semi standard non polar33892256
Aspalathin,4TMS,isomer #37C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3884.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #38C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3874.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #39C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3862.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3979.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #40C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3875.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #41C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3835.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #42C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3838.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #43C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3844.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #44C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3865.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #45C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3866.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #46C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3880.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #47C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3823.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #48C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3831.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #49C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3834.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3952.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #50C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3854.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #51C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3861.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #52C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3871.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #53C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3950.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #54C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3968.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #55C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3968.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #56C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4022.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #57C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C13981.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #58C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C13973.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #59C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13976.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3977.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #60C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O3913.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #61C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3902.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #62C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O3857.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #63C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3860.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #64C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3876.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #65C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3896.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #66C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3851.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #67C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3849.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #68C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3866.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #69C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3943.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3875.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #70C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3938.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #71C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3990.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #72C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14050.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #73C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14002.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #74C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O3913.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #75C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3905.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #76C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13994.4Semi standard non polar33892256
Aspalathin,4TMS,isomer #77C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3914.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #78C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3902.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #79C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3920.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3844.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #80C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3909.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #81C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3947.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #82C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3904.0Semi standard non polar33892256
Aspalathin,4TMS,isomer #83C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3845.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #84C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3879.7Semi standard non polar33892256
Aspalathin,4TMS,isomer #85C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3849.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #86C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3881.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #87C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3886.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #88C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3891.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #89C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3838.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3840.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #90C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3839.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #91C[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3994.8Semi standard non polar33892256
Aspalathin,4TMS,isomer #92C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C13985.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #93C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3872.9Semi standard non polar33892256
Aspalathin,4TMS,isomer #94C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3862.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #95C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3947.3Semi standard non polar33892256
Aspalathin,4TMS,isomer #96C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14002.6Semi standard non polar33892256
Aspalathin,4TMS,isomer #97C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3925.1Semi standard non polar33892256
Aspalathin,4TMS,isomer #98C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3915.2Semi standard non polar33892256
Aspalathin,4TMS,isomer #99C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3862.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O3858.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3903.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #100C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3887.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #101C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3833.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #102C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3883.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #103C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3842.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #104C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3835.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #105C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3829.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #106C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13904.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #107C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O3845.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #108C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)=CC=C1O3835.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #109C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3807.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3873.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #110C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3840.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #111C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3795.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #112C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3846.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #113C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3842.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #114C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3899.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #115C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3843.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #116C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3847.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #117C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3838.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #118C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3868.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #119C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3849.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3903.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #120C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3873.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #121C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O3846.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #122C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)=CC=C1O3844.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #123C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O)C=C1O[Si](C)(C)C3890.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #124C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3854.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #125C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3886.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #126C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3925.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3914.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3936.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3928.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3832.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3820.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3833.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3826.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3820.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3780.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3813.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3785.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3799.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3811.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3809.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3774.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3801.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3779.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3790.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3823.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3805.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3802.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3870.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3895.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3884.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3942.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #36C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3868.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #37C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3877.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #38C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3866.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #39C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3877.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3843.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #40C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3822.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #41C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3825.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #42C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3826.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #43C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3849.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #44C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3862.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #45C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3857.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #46C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3814.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #47C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3819.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #48C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3820.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #49C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3841.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3831.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #50C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3857.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #51C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3853.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #52C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3929.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #53C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3952.6Semi standard non polar33892256
Aspalathin,5TMS,isomer #54C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3944.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #55C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4008.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #56C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3820.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #57C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3821.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #58C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3824.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #59C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3844.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3821.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #60C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3857.6Semi standard non polar33892256
Aspalathin,5TMS,isomer #61C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3851.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #62C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3792.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #63C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3805.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #64C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3805.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #65C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3854.6Semi standard non polar33892256
Aspalathin,5TMS,isomer #66C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3783.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #67C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3798.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #68C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3797.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #69C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3850.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3820.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #70C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3954.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #71C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C13957.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #72C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13905.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #73C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O3848.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #74C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)=CC=C1O3840.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #75C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13895.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #76C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3834.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #77C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3823.6Semi standard non polar33892256
Aspalathin,5TMS,isomer #78C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3851.2Semi standard non polar33892256
Aspalathin,5TMS,isomer #79C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3847.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3837.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #80C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3888.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #81C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3830.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #82C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3805.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #83C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3847.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #84C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3801.3Semi standard non polar33892256
Aspalathin,5TMS,isomer #85C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3833.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #86C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3858.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #87C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3819.8Semi standard non polar33892256
Aspalathin,5TMS,isomer #88C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3796.7Semi standard non polar33892256
Aspalathin,5TMS,isomer #89C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3787.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3829.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #90C[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3914.9Semi standard non polar33892256
Aspalathin,5TMS,isomer #91C[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13969.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #92C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)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)C=C1O3895.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #93C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)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)=CC=C1O3888.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #94C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3842.6Semi standard non polar33892256
Aspalathin,5TMS,isomer #95C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3837.0Semi standard non polar33892256
Aspalathin,5TMS,isomer #96C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3903.4Semi standard non polar33892256
Aspalathin,5TMS,isomer #97C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3836.1Semi standard non polar33892256
Aspalathin,5TMS,isomer #98C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3826.5Semi standard non polar33892256
Aspalathin,5TMS,isomer #99C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3890.7Semi standard non polar33892256
Aspalathin,6TMS,isomer #1C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O3840.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #10C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3782.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #11C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3770.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #12C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3789.0Semi standard non polar33892256
Aspalathin,6TMS,isomer #13C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3771.0Semi standard non polar33892256
Aspalathin,6TMS,isomer #14C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3769.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #15C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3787.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #16C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3770.3Semi standard non polar33892256
Aspalathin,6TMS,isomer #17C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3832.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #18C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3854.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #19C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3841.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #2C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O3820.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #20C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3898.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #21C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3798.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #22C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3815.0Semi standard non polar33892256
Aspalathin,6TMS,isomer #23C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3797.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #24C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3795.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #25C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3812.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #26C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3797.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #27C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3755.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #28C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3769.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #29C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3760.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #3C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O3829.7Semi standard non polar33892256
Aspalathin,6TMS,isomer #30C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3782.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #31C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3735.3Semi standard non polar33892256
Aspalathin,6TMS,isomer #32C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3751.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #33C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3740.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #34C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3767.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #35C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3863.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #36C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3836.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #37C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3835.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #38C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3835.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #39C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3847.7Semi standard non polar33892256
Aspalathin,6TMS,isomer #4C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C3820.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #40C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3863.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #41C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3850.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #42C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3793.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #43C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3806.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #44C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3795.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #45C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3840.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #46C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3776.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #47C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3792.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #48C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3777.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #49C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3831.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #5C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O3782.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #50C[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3928.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #51C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3805.3Semi standard non polar33892256
Aspalathin,6TMS,isomer #52C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3819.7Semi standard non polar33892256
Aspalathin,6TMS,isomer #53C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C3804.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #54C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3849.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #55C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3793.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #56C[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C)=C3)=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C3784.3Semi standard non polar33892256
Aspalathin,6TMS,isomer #57C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C2O[Si](C)(C)C)C(O[Si](C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C13861.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #58C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O3794.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #59C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)=CC=C1O3784.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #6C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O3803.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #60C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3785.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #61C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3773.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #62C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3830.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #63C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3774.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #64C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3759.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #65C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3812.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #66C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3856.0Semi standard non polar33892256
Aspalathin,6TMS,isomer #67C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O3760.3Semi standard non polar33892256
Aspalathin,6TMS,isomer #68C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O)C=C1O[Si](C)(C)C3813.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #69C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3799.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #7C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C3783.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #70C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3788.5Semi standard non polar33892256
Aspalathin,6TMS,isomer #71C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)=CC=C1O3744.8Semi standard non polar33892256
Aspalathin,6TMS,isomer #72C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)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[Si](C)(C)C)C=C1O3816.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #73C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)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[Si](C)(C)C)=CC=C1O3801.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #74C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)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)C=C1O[Si](C)(C)C3882.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #75C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3842.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #76C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3834.6Semi standard non polar33892256
Aspalathin,6TMS,isomer #77C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3831.7Semi standard non polar33892256
Aspalathin,6TMS,isomer #78C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O3781.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #79C[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)=CC=C1O3767.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #8C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O3782.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #80C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C3816.1Semi standard non polar33892256
Aspalathin,6TMS,isomer #81C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3794.9Semi standard non polar33892256
Aspalathin,6TMS,isomer #82C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3838.4Semi standard non polar33892256
Aspalathin,6TMS,isomer #83C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3843.2Semi standard non polar33892256
Aspalathin,6TMS,isomer #84C[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C)C(O)C3O)=C2O[Si](C)(C)C)C=C1O[Si](C)(C)C3847.3Semi standard non polar33892256
Aspalathin,6TMS,isomer #9C[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C3799.2Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4405.7Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1C(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)OC(CO)C(O)C1O4468.4Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C1O4475.6Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C1O4454.7Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O)C1O4463.2Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14468.2Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4430.6Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4458.3Semi standard non polar33892256
Aspalathin,1TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O)C1O4455.1Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4572.4Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14615.8Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)C=C1O4553.0Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)=CC=C1O4523.5Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4592.9Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C1O4565.3Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1C(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C4583.9Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C1O[Si](C)(C)C(C)(C)C4567.9Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4567.0Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14602.2Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)C=C1O4529.1Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4595.9Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)=CC=C1O4498.7Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4576.6Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4567.2Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14592.7Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)C=C1O4528.4Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)=CC=C1O4501.0Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4580.4Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2OC(CO)C(O)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14635.0Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4613.9Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4581.0Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O4540.3Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O4653.2Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14671.1Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4641.6Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4611.3Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)=CC=C1O4603.4Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C(C)(C)C4581.2Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)C=C1O4624.3Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O)C(O)C1O4514.5Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4588.8Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4560.2Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4551.5Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4537.2Semi standard non polar33892256
Aspalathin,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4587.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O4748.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4756.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4736.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4730.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4710.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O)C(O)C1O4673.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4682.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4634.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4642.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4627.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4659.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O4695.5Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4612.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4610.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4603.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4685.5Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4681.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4671.1Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4675.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4688.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4676.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14753.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O)C(O)C1O4662.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)C=C1O4706.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)=CC=C1O4670.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4748.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4681.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4681.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O[Si](C)(C)C(C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14720.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #36CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O[Si](C)(C)C(C)(C)C)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14719.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #37CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O)C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14766.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #38CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)C=C1O4739.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #39CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)=CC=C1O4709.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4728.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #40CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)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)C=C1O4631.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #41CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)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)C=C1O4638.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #42CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O[Si](C)(C)C(C)(C)C)C=C1O4700.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #43CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O)C=C1O[Si](C)(C)C(C)(C)C4688.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #44CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)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)=CC=C1O4601.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #45CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)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)=CC=C1O4609.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #46CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)=C2O[Si](C)(C)C(C)(C)C)=CC=C1O4675.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #47CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4677.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #48CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4677.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #49CC(C)(C)[Si](C)(C)OC1C(CO)OC(C2=C(O)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4672.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4696.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #50CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4672.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #51CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14708.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #52CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)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)C=C1O4634.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #53CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)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)=CC=C1O4605.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #54CC(C)(C)[Si](C)(C)OC1=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O)=CC(O)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4665.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #55CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14736.5Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #56CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)C=C1O4691.1Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #57CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)=CC=C1O4661.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #58CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4723.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #59CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C2O)C(O[Si](C)(C)C(C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14747.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4696.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #60CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)C=C1O4711.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #61CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)=CC=C1O4679.1Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #62CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O[Si](C)(C)C(C)(C)C)C=C1O4674.4Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #63CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O)C=C1O[Si](C)(C)C(C)(C)C4656.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #64CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)=C2O[Si](C)(C)C(C)(C)C)=CC=C1O4650.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #65CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O)=C1C(=O)CCC1=CC=C(O)C(O)=C14732.5Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #66CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)C=C1O4685.1Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #67CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)=CC=C1O4652.1Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #68CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C(=O)CCC2=CC=C(O)C(O)=C2)C(O[Si](C)(C)C(C)(C)C)=C1C1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4723.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #69CC(C)(C)[Si](C)(C)OC1=CC(O)=C(C2OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14749.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C(=O)CCC3=CC=C(O)C(O)=C3)=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4683.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #70CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)C=C1O4708.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #71CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)=CC=C1O4678.1Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #72CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)C=C1O4672.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #73CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O)C=C1O[Si](C)(C)C(C)(C)C4659.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #74CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)=CC=C1O4646.7Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #75CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C(C2OC(CO)C(O)C(O)C2O)C(O[Si](C)(C)C(C)(C)C)=C1C(=O)CCC1=CC=C(O)C(O)=C14828.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #76CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O4805.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #77CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)=CC=C1O4766.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #78CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)C=C1O4789.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #79CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C(C)(C)C4773.9Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)=C2O)C(O)C(O)C1O4725.3Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #80CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)=CC=C1O4755.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #81CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)C=C1O4831.0Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #82CC(C)(C)[Si](C)(C)OC1=CC(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)=CC=C1O4805.2Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #83CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O[Si](C)(C)C(C)(C)C)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O)C=C1O[Si](C)(C)C(C)(C)C4806.6Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #84CC(C)(C)[Si](C)(C)OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C(C3OC(CO)C(O)C(O)C3O)=C2O[Si](C)(C)C(C)(C)C)C=C1O[Si](C)(C)C(C)(C)C4770.8Semi standard non polar33892256
Aspalathin,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC1OC(C2=C(O)C=C(O[Si](C)(C)C(C)(C)C)C(C(=O)CCC3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)=C2O)C(O)C(O)C1O4695.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (Non-derivatized) - 70eV, Positivesplash10-0uk9-3319300000-45376cbf9a2d6e1a77392017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (3 TMS) - 70eV, Positivesplash10-0udi-1503239000-a78101e94cc6cb2a02ea2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_4_70) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_5_32) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_5_75) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_5_84) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_5_89) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_5_90) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_17) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_27) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_31) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_57) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_63) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_64) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_67) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_70) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS (TMS_6_71) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Aspalathin GC-MS ("Aspalathin,4TMS,#70" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Aspalathin LC-ESI-TOF , negative-QTOFsplash10-001i-0009000000-01e32f1179b48e5ee0e92017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Aspalathin LC-ESI-TOF , negative-QTOFsplash10-001i-0339000000-31d4a128639c392358602017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Aspalathin LC-ESI-TOF , negative-QTOFsplash10-0udi-0004900000-8a9fed14120bd0eec3092017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Aspalathin LC-ESI-TOF , negative-QTOFsplash10-0699-0930000000-293fd3162e6a0e0b86982017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Aspalathin LC-ESI-TOF , negative-QTOFsplash10-00n0-0900000000-317267c2e005616454de2017-09-14HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 10V, Positive-QTOFsplash10-0udr-0111900000-f0d7b6fbf0f247cee2f22016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 20V, Positive-QTOFsplash10-00rj-2936500000-fc22621b3a633d81573b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 40V, Positive-QTOFsplash10-0fsc-1944100000-3e2e9b1902773f1940362016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 10V, Negative-QTOFsplash10-0udi-0122900000-ab59ac2515024cdfa74b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 20V, Negative-QTOFsplash10-0fes-7954500000-ec312484c9eaa9c877642016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 40V, Negative-QTOFsplash10-0006-9553000000-4620713bad1e4f20d6c12016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 10V, Positive-QTOFsplash10-0udi-0202900000-ae0e1f2b5330590475372021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 20V, Positive-QTOFsplash10-0fek-1903300000-9f425cbfef4422a0b51c2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 40V, Positive-QTOFsplash10-05mk-8901100000-db87b41479ac20cb8eb52021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 10V, Negative-QTOFsplash10-0udi-0013900000-1b009e58ade9e5d281bb2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 20V, Negative-QTOFsplash10-0pwi-1249800000-7959974db22200facb9e2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Aspalathin 40V, Negative-QTOFsplash10-000i-4911100000-de95629a541dded320832021-09-25Wishart 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 IDFDB002810
KNApSAcK IDC00006096
Chemspider ID24846098
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkAspalathin
METLIN IDNot Available
PubChem Compound16752601
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
Aspalathin → 3-(4-hydroxy-3-methoxyphenyl)-1-{2,4,6-trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}propan-1-onedetails
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
Aspalathin → [(6-{3-[3-(3,4-dihydroxyphenyl)propanoyl]-2,4,6-trihydroxyphenyl}-3,4,5-trihydroxyoxan-2-yl)methoxy]sulfonic aciddetails
Aspalathin → (6-{3-[3-(3,4-dihydroxyphenyl)propanoyl]-2,4,6-trihydroxyphenyl}-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl)oxidanesulfonic aciddetails
Aspalathin → (2-{3-[3-(3,4-dihydroxyphenyl)propanoyl]-2,4,6-trihydroxyphenyl}-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl)oxidanesulfonic aciddetails
Aspalathin → (2-{3-[3-(3,4-dihydroxyphenyl)propanoyl]-2,4,6-trihydroxyphenyl}-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
Aspalathin → 6-{2-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenoxy}-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
Aspalathin → 3,4,5-trihydroxy-6-[2-hydroxy-4-(3-oxo-3-{2,4,6-trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}propyl)phenoxy]oxane-2-carboxylic aciddetails
Aspalathin → 3,4,5-trihydroxy-6-[2-hydroxy-5-(3-oxo-3-{2,4,6-trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}propyl)phenoxy]oxane-2-carboxylic aciddetails
Aspalathin → 6-{2-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenoxy}-3,4,5-trihydroxyoxane-2-carboxylic aciddetails
Aspalathin → 6-{4-[3-(3,4-dihydroxyphenyl)propanoyl]-3,5-dihydroxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenoxy}-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
Aspalathin → [2-hydroxy-5-(3-oxo-3-{2,4,6-trihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl}propyl)phenyl]oxidanesulfonic aciddetails