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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 18:33:29 UTC
Update Date2022-03-07 02:53:51 UTC
HMDB IDHMDB0033795
Secondary Accession Numbers
  • HMDB33795
Metabolite Identification
Common NameQuercetin 3-arabinoside
DescriptionQuercetin 3-arabinoside belongs to the class of organic compounds known as curcuminoids. These are aromatic compounds containing a curcumin moiety, which is composed of two aryl buten-2-one (feruloyl) chromophores joined by a methylene group. Quercetin 3-arabinoside has been detected, but not quantified in, several different foods, such as apples (Malus pumila), fennels (Foeniculum vulgare), anises (Pimpinella anisum), bilberries (Vaccinium myrtillus), and common walnuts (Juglans regia). This could make quercetin 3-arabinoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Quercetin 3-arabinoside.
Structure
Data?1563862461
Synonyms
ValueSource
GuaiaverinHMDB
GuaijaverinHMDB
GuajavarinHMDB, MeSH
Quercetin 3-L-arabinosideHMDB
Quercetin 3-O-alpha-L-arabinopyranosideHMDB
Quercetin 3-O-alpha-L-arabinosideHMDB, MeSH
Quercetin 3-O-arabinosideHMDB
Chemical FormulaC20H18O11
Average Molecular Weight434.3503
Monoisotopic Molecular Weight434.084911418
IUPAC Name3-{[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4H-chromen-4-one
Traditional Name3-{[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy}-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one
CAS Registry Number22255-13-6
SMILES
OC[C@@H]1O[C@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O
InChI Identifier
InChI=1S/C20H18O11/c21-6-13-15(26)17(28)20(30-13)31-19-16(27)14-11(25)4-8(22)5-12(14)29-18(19)7-1-2-9(23)10(24)3-7/h1-5,13,15,17,20-26,28H,6H2/t13-,15-,17+,20+/m0/s1
InChI KeyBDCDNTVZSILEOY-BQCJVYABSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as curcuminoids. These are aromatic compounds containing a curcumin moiety, which is composed of two aryl buten-2-one (feruloyl) chromophores joined by a methylene group.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassDiarylheptanoids
Sub ClassLinear diarylheptanoids
Direct ParentCurcuminoids
Alternative Parents
Substituents
  • Desmethoxycurcumin
  • Hydroxycinnamic acid or derivatives
  • Methoxyphenol
  • Anisole
  • Phenoxy compound
  • Phenol ether
  • Styrene
  • Methoxybenzene
  • Phenol
  • 1,3-diketone
  • Alkyl aryl ether
  • 1-hydroxy-2-unsubstituted benzenoid
  • Benzenoid
  • 1,3-dicarbonyl compound
  • Monocyclic benzene moiety
  • Acryloyl-group
  • Alpha,beta-unsaturated ketone
  • Enone
  • Ketone
  • Ether
  • Organooxygen compound
  • Carbonyl group
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point239 °CNot Available
Boiling Point828.10 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility6882 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP1.680 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.15 g/LALOGPS
logP0.76ALOGPS
logP0.49ChemAxon
logS-2.6ALOGPS
pKa (Strongest Acidic)6.43ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area186.37 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity103.31 m³·mol⁻¹ChemAxon
Polarizability41.06 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+193.1430932474
DeepCCS[M-H]-190.74530932474
DeepCCS[M-2H]-223.88530932474
DeepCCS[M+Na]+199.05330932474
AllCCS[M+H]+198.832859911
AllCCS[M+H-H2O]+196.232859911
AllCCS[M+NH4]+201.232859911
AllCCS[M+Na]+201.932859911
AllCCS[M-H]-196.532859911
AllCCS[M+Na-2H]-196.532859911
AllCCS[M+HCOO]-196.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Quercetin 3-arabinosideOC[C@@H]1O[C@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O5999.8Standard polar33892256
Quercetin 3-arabinosideOC[C@@H]1O[C@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O4001.0Standard non polar33892256
Quercetin 3-arabinosideOC[C@@H]1O[C@H](OC2=C(OC3=C(C(O)=CC(O)=C3)C2=O)C2=CC=C(O)C(O)=C2)[C@H](O)[C@H]1O4170.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Quercetin 3-arabinoside,1TMS,isomer #1C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4104.1Semi standard non polar33892256
Quercetin 3-arabinoside,1TMS,isomer #2C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O)[C@H]1O)=C(C1=CC=C(O)C(O)=C1)O24071.5Semi standard non polar33892256
Quercetin 3-arabinoside,1TMS,isomer #3C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C14128.6Semi standard non polar33892256
Quercetin 3-arabinoside,1TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4072.4Semi standard non polar33892256
Quercetin 3-arabinoside,1TMS,isomer #5C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O4059.5Semi standard non polar33892256
Quercetin 3-arabinoside,1TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO)O[C@@H]1OC1=C(C2=CC=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1=O4155.2Semi standard non polar33892256
Quercetin 3-arabinoside,1TMS,isomer #7C[Si](C)(C)O[C@H]1[C@H](CO)O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O4146.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #1C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O3996.4Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #10C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O)=C(C1=CC=C(O)C(O)=C1)O24031.3Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #11C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O24033.9Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #12C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C14043.3Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #13C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C14052.8Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #14C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13985.3Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #15C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13974.1Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #16C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4008.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4017.4Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3954.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #19C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O3991.2Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #2C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O3976.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #20C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O4001.9Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #21C[Si](C)(C)O[C@H]1[C@H](CO)O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O[Si](C)(C)C4075.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #3C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4019.6Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #4C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4008.5Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #5C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O4051.9Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #6C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C4054.6Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #7C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C13995.6Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #8C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3985.5Semi standard non polar33892256
Quercetin 3-arabinoside,2TMS,isomer #9C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1O3970.8Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #1C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O3910.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #10C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3928.2Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #11C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3973.1Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #12C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3986.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #13C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3971.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #14C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3987.2Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #15C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3990.2Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #16C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C13921.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #17C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C13931.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #18C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13943.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #19C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13944.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #2C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O3887.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3888.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3900.8Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #22C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3874.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #23C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1O3875.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #24C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1O3891.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #25C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)=C(C1=CC=C(O)C(O)=C1)O23974.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #26C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C13985.6Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13887.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #28C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13878.1Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #29C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13904.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #3C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3896.3Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #30C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13896.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13880.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #32C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O3946.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3912.6Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3924.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #35C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O3932.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #4C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3947.3Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #5C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3954.1Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #6C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O3873.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #7C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3880.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #8C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3926.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TMS,isomer #9C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3932.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #1C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O3834.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #10C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3885.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #11C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3864.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #12C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3810.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #13C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3808.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #14C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3804.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #15C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3803.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #16C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3871.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #17C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3882.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #18C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3880.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #19C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3934.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #2C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3826.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #20C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3919.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #21C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C13893.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #22C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13887.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #23C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13884.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #24C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13892.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #25C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13890.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #26C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13895.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O3823.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3810.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #29C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3819.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #3C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3877.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #30C[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1O3812.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #31C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13837.3Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #32C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13829.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #33C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13826.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #34C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13835.9Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #35C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3886.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #4C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3878.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #5C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3874.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #6C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3826.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #7C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3825.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #8C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3821.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TMS,isomer #9C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3821.5Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #1C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O3856.7Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #10C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3784.5Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #11C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3837.1Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #12C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3851.4Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #13C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3788.0Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #14C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3770.6Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #15C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3834.2Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #16C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC2=C13866.3Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #17C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC2=C13862.4Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #18C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13863.2Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #19C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13864.3Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #2C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3810.9Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #20C[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C3815.9Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #21C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13832.1Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #3C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3810.2Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #4C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3801.5Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #5C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3799.7Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #6C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3852.6Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #7C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3843.8Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #8C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3855.6Semi standard non polar33892256
Quercetin 3-arabinoside,5TMS,isomer #9C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3800.4Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #1C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O3836.5Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #2C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C3841.6Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #3C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3809.8Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #4C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3796.6Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #5C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3826.6Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #6C[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C)=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C3828.2Semi standard non polar33892256
Quercetin 3-arabinoside,6TMS,isomer #7C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C13860.8Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4380.2Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O)[C@H]1O)=C(C1=CC=C(O)C(O)=C1)O24359.4Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C14375.5Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4363.4Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O4338.7Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](CO)O[C@@H]1OC1=C(C2=CC=C(O)C(O)=C2)OC2=CC(O)=CC(O)=C2C1=O4408.0Semi standard non polar33892256
Quercetin 3-arabinoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO)O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O4402.2Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4476.8Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)=C(C1=CC=C(O)C(O)=C1)O24501.1Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC=C(O)C(O)=C1)O24503.2Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C14517.7Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C14523.9Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14494.3Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14466.2Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4489.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4497.8Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4432.8Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O4464.2Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4449.1Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O4471.9Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)O[C@H]1[C@H](CO)O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@@H]1O[Si](C)(C)C(C)(C)C4548.7Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4493.4Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4486.4Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4516.5Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4520.0Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C14472.5Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4483.8Semi standard non polar33892256
Quercetin 3-arabinoside,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1O4454.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4564.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4585.6Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4616.1Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4613.3Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4600.2Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4599.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4637.2Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O)=C3)OC2=C14601.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C14609.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14674.3Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14635.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4591.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4601.1Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4610.3Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4560.3Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1O4566.8Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1O4575.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@H]1O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC=C(O)C(O)=C1)O24626.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C14646.1Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14615.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14582.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14626.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4585.6Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14593.2Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14570.8Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O4612.6Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4574.7Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4584.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1O4590.0Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4592.8Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4588.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4556.5Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4549.4Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4565.9Semi standard non polar33892256
Quercetin 3-arabinoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4560.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4685.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4681.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4742.9Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4682.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4681.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4663.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4666.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4655.3Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4678.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4674.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4719.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4671.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C4683.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O)=C3)OC2=C14678.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14820.2Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14785.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14814.9Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14779.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14748.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O4701.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4680.7Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4676.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4675.5Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1O4673.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14720.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14693.8Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14700.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@H]3O[C@@H](CO)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14699.4Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@H]3O[C@@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C1O[Si](C)(C)C(C)(C)C4676.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4664.1Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O4781.9Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4714.6Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4712.3Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O4701.0Semi standard non polar33892256
Quercetin 3-arabinoside,4TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@@H]1O[C@H](OC2=C(C3=CC=C(O[Si](C)(C)C(C)(C)C)C(O)=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4702.8Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Quercetin 3-arabinoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-074l-9002200000-2d25b1439162975be1892017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Quercetin 3-arabinoside GC-MS (3 TMS) - 70eV, Positivesplash10-000i-6900016000-052fe746be5b262723302017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Quercetin 3-arabinoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 10V, Positive-QTOFsplash10-0udr-1239700000-28b26f9b0787af6359a82016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 20V, Positive-QTOFsplash10-0udi-0269100000-7a94db25e6a9fec0926f2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 40V, Positive-QTOFsplash10-0f79-3972000000-fc79be30bd59abcaa2682016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 10V, Negative-QTOFsplash10-0f89-1115900000-e00178a2826bcd7052652016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 20V, Negative-QTOFsplash10-0ue9-0649200000-08c4ad36ee9b747c16032016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 40V, Negative-QTOFsplash10-0zgr-2952000000-5bfe8c304eb8f6a070512016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 10V, Negative-QTOFsplash10-001i-0000900000-5783c018f9dec347d81f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 20V, Negative-QTOFsplash10-0f89-0300900000-54efe938cd8127c33b3b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 40V, Negative-QTOFsplash10-0ue9-1910200000-7f4dea7cc660d252c92f2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 10V, Positive-QTOFsplash10-000i-0000900000-1453f61e7eeaeb92b36b2021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 20V, Positive-QTOFsplash10-000i-0000900000-a73a1bd1968f25a6dee42021-09-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Quercetin 3-arabinoside 40V, Positive-QTOFsplash10-0udr-1911300000-24dd47b5a2f4224e16022021-09-24Wishart 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 IDFDB011955
KNApSAcK IDC00053738
Chemspider ID8427825
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound10252339
PDB IDNot Available
ChEBI ID167916
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1485731
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.. .