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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 22:40:39 UTC
Update Date2022-03-07 02:55:19 UTC
HMDB IDHMDB0037429
Secondary Accession Numbers
  • HMDB37429
Metabolite Identification
Common NameAstragalin
DescriptionAstragalin belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position. Thus, astragalin is considered to be a flavonoid. Astragalin is found, on average, in the highest concentration within a few different foods, such as yellow wax beans (Phaseolus vulgaris), green beans (Phaseolus vulgaris), and common beans (Phaseolus vulgaris) and in a lower concentration in red raspberries (Rubus idaeus), broad beans (Vicia faba), and teas (Camellia sinensis). Astragalin has also been detected, but not quantified in, several different foods, such as black chokeberries (Photinia melanocarpa), grapefruit/pummelo hybrids (Citrus paradisi X Citrus maxima), arabica coffees (Coffea arabica), eggplants (Solanum melongena), and mugworts (Artemisia vulgaris). This could make astragalin a potential biomarker for the consumption of these foods. Astragalin is a secondary metabolite. Secondary metabolites are metabolically or physiologically non-essential metabolites that may serve a role as defense or signalling molecules. In some cases they are simply molecules that arise from the incomplete metabolism of other secondary metabolites. Based on a literature review a small amount of articles have been published on Astragalin.
Structure
Data?1563863029
Synonyms
ValueSource
3,4',5,7-Tetrahydroxyflavone-3-glucosideChEBI
5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl beta-D-glucopyranosideChEBI
AstragalineChEBI
Kaempferol 3-O-glucosideChEBI
Kaempferol-3-O-beta-glucopyranosideChEBI
Kaempferol 3-O-beta-D-glucosideKegg
5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl b-D-glucopyranosideGenerator
5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-3-yl β-D-glucopyranosideGenerator
Kaempferol-3-O-b-glucopyranosideGenerator
Kaempferol-3-O-β-glucopyranosideGenerator
Kaempferol 3-O-b-D-glucosideGenerator
Kaempferol 3-O-β-D-glucosideGenerator
Kaempferol 3-O-beta-D-glucopyranosideMeSH
AstragalinChEBI
3,4',5,7-TetrahydroxyflavoneHMDB
3-O-b-D-GlucopyranosideHMDB
3-O-b-D-Glucopyranosyloxy-4',5,7-trihydroxyflavoneHMDB
AsragalinHMDB
Kaempferol 3-glucosideHMDB
Kaempferol-3-beta-glucopyranosideHMDB
Kaempferol-3-beta-monoglucosideHMDB
Kaempferol-3-D-glucosideHMDB
Kaempferol-3-glucosideHMDB
Kaempferol-3-O-glucosideHMDB
3-GlucosylkaempferolPhytoBank
4',5,7-Trihydroxyflavone 3-beta-D-glucopyranosidePhytoBank
4',5,7-Trihydroxyflavone 3-β-D-glucopyranosidePhytoBank
4’,5,7-Trihydroxyflavone 3-β-D-glucopyranosidePhytoBank
Kaemferol 3-O-glucopyranosidePhytoBank
Kaempferol 3-O-glucopyranosidePhytoBank
Kaempferol 3-O-β-D-glucopyranosidePhytoBank
Kaempferol 3-O-beta-glucosidePhytoBank
Kaempferol 3-O-β-glucosidePhytoBank
Kaempferol 3-beta-D-glucopyranosidePhytoBank
Kaempferol 3-β-D-glucopyranosidePhytoBank
Kaempferol 3-beta-D-glucosidePhytoBank
Kaempferol 3-β-D-glucosidePhytoBank
Kaempherol 3-O-beta-D-glucopyranosidePhytoBank
Kaempherol 3-O-β-D-glucopyranosidePhytoBank
Chemical FormulaC21H20O11
Average Molecular Weight448.3769
Monoisotopic Molecular Weight448.100561482
IUPAC Name5,7-dihydroxy-2-(4-hydroxyphenyl)-3-{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-4H-chromen-4-one
Traditional Nameastragalin
CAS Registry Number480-10-4
SMILES
OC[C@H]1O[C@@H](OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O
InChI Identifier
InChI=1S/C21H20O11/c22-7-13-15(26)17(28)18(29)21(31-13)32-20-16(27)14-11(25)5-10(24)6-12(14)30-19(20)8-1-3-9(23)4-2-8/h1-6,13,15,17-18,21-26,28-29H,7H2/t13-,15-,17+,18-,21+/m1/s1
InChI KeyJPUKWEQWGBDDQB-QSOFNFLRSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid-3-o-glycosides. These are phenolic compounds containing a flavonoid moiety which is O-glycosidically linked to carbohydrate moiety at the C3-position.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid-3-O-glycosides
Alternative Parents
Substituents
  • Flavonoid-3-o-glycoside
  • 4'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Hexose monosaccharide
  • Chromone
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Phenol
  • Pyranone
  • Pyran
  • Monocyclic benzene moiety
  • Oxane
  • Monosaccharide
  • Benzenoid
  • Heteroaromatic compound
  • Vinylogous acid
  • Secondary alcohol
  • Organoheterocyclic compound
  • Oxacycle
  • Acetal
  • Polyol
  • Hydrocarbon derivative
  • Organic oxide
  • Organic oxygen compound
  • Alcohol
  • Primary alcohol
  • Organooxygen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
Process
Role
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point178 °CNot Available
Boiling Point296.00 to 297.00 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility1.87 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP4.397 (est)The Good Scents Company Information System
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.58 g/LALOGPS
logP0.52ALOGPS
logP0.16ChemAxon
logS-2.4ALOGPS
pKa (Strongest Acidic)6.37ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area186.37 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity107.29 m³·mol⁻¹ChemAxon
Polarizability42.39 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]+192.930932474
DeepCCS[M-H]-190.50530932474
DeepCCS[M-2H]-223.54530932474
DeepCCS[M+Na]+198.81330932474
AllCCS[M+H]+202.532859911
AllCCS[M+H-H2O]+200.132859911
AllCCS[M+NH4]+204.832859911
AllCCS[M+Na]+205.532859911
AllCCS[M-H]-199.732859911
AllCCS[M+Na-2H]-200.032859911
AllCCS[M+HCOO]-200.432859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
AstragalinOC[C@H]1O[C@@H](OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O5648.3Standard polar33892256
AstragalinOC[C@H]1O[C@@H](OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O4182.4Standard non polar33892256
AstragalinOC[C@H]1O[C@@H](OC2=C(OC3=CC(O)=CC(O)=C3C2=O)C2=CC=C(O)C=C2)[C@H](O)[C@@H](O)[C@@H]1O4320.6Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Astragalin,1TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4133.5Semi standard non polar33892256
Astragalin,1TMS,isomer #2C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14225.8Semi standard non polar33892256
Astragalin,1TMS,isomer #3C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C(C1=CC=C(O)C=C1)O24188.5Semi standard non polar33892256
Astragalin,1TMS,isomer #4C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14210.1Semi standard non polar33892256
Astragalin,1TMS,isomer #5C[Si](C)(C)O[C@H]1[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@@H](O)[C@@H]1O4170.8Semi standard non polar33892256
Astragalin,1TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@H]1O4156.6Semi standard non polar33892256
Astragalin,1TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4148.3Semi standard non polar33892256
Astragalin,2TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4042.0Semi standard non polar33892256
Astragalin,2TMS,isomer #10C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C14095.1Semi standard non polar33892256
Astragalin,2TMS,isomer #11C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C14084.0Semi standard non polar33892256
Astragalin,2TMS,isomer #12C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C14078.8Semi standard non polar33892256
Astragalin,2TMS,isomer #13C[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](O)[C@H]1O)=C(C1=CC=C(O)C=C1)O24067.0Semi standard non polar33892256
Astragalin,2TMS,isomer #14C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O)=C(C1=CC=C(O)C=C1)O24072.9Semi standard non polar33892256
Astragalin,2TMS,isomer #15C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C)=C(C1=CC=C(O)C=C1)O24083.3Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14047.5Semi standard non polar33892256
Astragalin,2TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14065.3Semi standard non polar33892256
Astragalin,2TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14074.9Semi standard non polar33892256
Astragalin,2TMS,isomer #19C[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@@H]1CO4043.5Semi standard non polar33892256
Astragalin,2TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4046.4Semi standard non polar33892256
Astragalin,2TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@H]1O4059.9Semi standard non polar33892256
Astragalin,2TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](CO)O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C4043.2Semi standard non polar33892256
Astragalin,2TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4033.6Semi standard non polar33892256
Astragalin,2TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O4042.1Semi standard non polar33892256
Astragalin,2TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O4035.5Semi standard non polar33892256
Astragalin,2TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C4046.3Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14087.2Semi standard non polar33892256
Astragalin,2TMS,isomer #8C[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](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14069.1Semi standard non polar33892256
Astragalin,2TMS,isomer #9C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14079.6Semi standard non polar33892256
Astragalin,3TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O3949.6Semi standard non polar33892256
Astragalin,3TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3976.5Semi standard non polar33892256
Astragalin,3TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3960.0Semi standard non polar33892256
Astragalin,3TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3985.1Semi standard non polar33892256
Astragalin,3TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3997.7Semi standard non polar33892256
Astragalin,3TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C4030.4Semi standard non polar33892256
Astragalin,3TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4003.9Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C13957.3Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C13959.5Semi standard non polar33892256
Astragalin,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](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13963.1Semi standard non polar33892256
Astragalin,3TMS,isomer #19C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C14016.2Semi standard non polar33892256
Astragalin,3TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O3943.6Semi standard non polar33892256
Astragalin,3TMS,isomer #20C[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](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C13975.7Semi standard non polar33892256
Astragalin,3TMS,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](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13982.1Semi standard non polar33892256
Astragalin,3TMS,isomer #22C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13964.5Semi standard non polar33892256
Astragalin,3TMS,isomer #23C[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13999.2Semi standard non polar33892256
Astragalin,3TMS,isomer #24C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13957.0Semi standard non polar33892256
Astragalin,3TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13975.4Semi standard non polar33892256
Astragalin,3TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C13960.8Semi standard non polar33892256
Astragalin,3TMS,isomer #27C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C13957.3Semi standard non polar33892256
Astragalin,3TMS,isomer #28C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C13968.5Semi standard non polar33892256
Astragalin,3TMS,isomer #29C[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](O[Si](C)(C)C)[C@H]1O)=C(C1=CC=C(O)C=C1)O23968.5Semi standard non polar33892256
Astragalin,3TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3987.2Semi standard non polar33892256
Astragalin,3TMS,isomer #30C[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](O)[C@H]1O[Si](C)(C)C)=C(C1=CC=C(O)C=C1)O23971.0Semi standard non polar33892256
Astragalin,3TMS,isomer #31C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)=C(C1=CC=C(O)C=C1)O23988.2Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C13975.6Semi standard non polar33892256
Astragalin,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](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C13981.6Semi standard non polar33892256
Astragalin,3TMS,isomer #34C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C13995.9Semi standard non polar33892256
Astragalin,3TMS,isomer #35C[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@H]1O[Si](C)(C)C3990.2Semi standard non polar33892256
Astragalin,3TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3970.1Semi standard non polar33892256
Astragalin,3TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3996.8Semi standard non polar33892256
Astragalin,3TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O3943.6Semi standard non polar33892256
Astragalin,3TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3983.4Semi standard non polar33892256
Astragalin,3TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3963.5Semi standard non polar33892256
Astragalin,3TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3989.9Semi standard non polar33892256
Astragalin,4TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O3926.7Semi standard non polar33892256
Astragalin,4TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3957.8Semi standard non polar33892256
Astragalin,4TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O)[C@@H]1O3893.0Semi standard non polar33892256
Astragalin,4TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3862.2Semi standard non polar33892256
Astragalin,4TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3906.3Semi standard non polar33892256
Astragalin,4TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3947.5Semi standard non polar33892256
Astragalin,4TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3966.1Semi standard non polar33892256
Astragalin,4TMS,isomer #16C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3947.3Semi standard non polar33892256
Astragalin,4TMS,isomer #17C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3935.2Semi standard non polar33892256
Astragalin,4TMS,isomer #18C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3955.0Semi standard non polar33892256
Astragalin,4TMS,isomer #19C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3935.2Semi standard non polar33892256
Astragalin,4TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3919.6Semi standard non polar33892256
Astragalin,4TMS,isomer #20C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C4020.4Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C13887.7Semi standard non polar33892256
Astragalin,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](O)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13876.3Semi standard non polar33892256
Astragalin,4TMS,isomer #23C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C13946.2Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13895.7Semi standard non polar33892256
Astragalin,4TMS,isomer #25C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C13940.0Semi standard non polar33892256
Astragalin,4TMS,isomer #26C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C13940.2Semi standard non polar33892256
Astragalin,4TMS,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](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13962.2Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13917.4Semi standard non polar33892256
Astragalin,4TMS,isomer #29C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13913.6Semi standard non polar33892256
Astragalin,4TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3888.1Semi standard non polar33892256
Astragalin,4TMS,isomer #30C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13926.2Semi standard non polar33892256
Astragalin,4TMS,isomer #31C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[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=C13898.0Semi standard non polar33892256
Astragalin,4TMS,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](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)C=C13895.6Semi standard non polar33892256
Astragalin,4TMS,isomer #33C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C13906.4Semi standard non polar33892256
Astragalin,4TMS,isomer #34C[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](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)=C(C1=CC=C(O)C=C1)O23941.8Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C13962.9Semi standard non polar33892256
Astragalin,4TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3932.6Semi standard non polar33892256
Astragalin,4TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O3905.6Semi standard non polar33892256
Astragalin,4TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3873.5Semi standard non polar33892256
Astragalin,4TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3918.8Semi standard non polar33892256
Astragalin,4TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3955.6Semi standard non polar33892256
Astragalin,4TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3980.8Semi standard non polar33892256
Astragalin,5TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(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](O)[C@@H]1O3901.3Semi standard non polar33892256
Astragalin,5TMS,isomer #10C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3953.4Semi standard non polar33892256
Astragalin,5TMS,isomer #11C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O[Si](C)(C)C)[C@@H]1O3854.1Semi standard non polar33892256
Astragalin,5TMS,isomer #12C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O)[C@@H]1O[Si](C)(C)C3853.2Semi standard non polar33892256
Astragalin,5TMS,isomer #13C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3856.9Semi standard non polar33892256
Astragalin,5TMS,isomer #14C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3946.4Semi standard non polar33892256
Astragalin,5TMS,isomer #15C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3931.9Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C13873.8Semi standard non polar33892256
Astragalin,5TMS,isomer #17C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C13930.6Semi standard non polar33892256
Astragalin,5TMS,isomer #18C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C3O2)C=C13920.9Semi standard non polar33892256
Astragalin,5TMS,isomer #19C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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[Si](C)(C)C)C=C3O2)C=C13922.5Semi standard non polar33892256
Astragalin,5TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O3885.8Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C(=O)C3=C(O)C=C(O[Si](C)(C)C)C=C3O2)C=C13924.8Semi standard non polar33892256
Astragalin,5TMS,isomer #21C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[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=C13894.5Semi standard non polar33892256
Astragalin,5TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C3910.8Semi standard non polar33892256
Astragalin,5TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3899.0Semi standard non polar33892256
Astragalin,5TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3905.6Semi standard non polar33892256
Astragalin,5TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3902.4Semi standard non polar33892256
Astragalin,5TMS,isomer #7C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O3877.3Semi standard non polar33892256
Astragalin,5TMS,isomer #8C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C3883.1Semi standard non polar33892256
Astragalin,5TMS,isomer #9C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3882.6Semi standard non polar33892256
Astragalin,6TMS,isomer #1C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(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](O[Si](C)(C)C)[C@@H]1O3897.6Semi standard non polar33892256
Astragalin,6TMS,isomer #2C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(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](O)[C@@H]1O[Si](C)(C)C3897.7Semi standard non polar33892256
Astragalin,6TMS,isomer #3C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3911.6Semi standard non polar33892256
Astragalin,6TMS,isomer #4C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O[Si](C)(C)C)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3922.0Semi standard non polar33892256
Astragalin,6TMS,isomer #5C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O[Si](C)(C)C)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C)=C3C2=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3902.2Semi standard non polar33892256
Astragalin,6TMS,isomer #6C[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C3874.1Semi standard non polar33892256
Astragalin,6TMS,isomer #7C[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O[Si](C)(C)C)[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[Si](C)(C)C)C=C3O2)C=C13931.3Semi standard non polar33892256
Astragalin,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4417.0Semi standard non polar33892256
Astragalin,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14465.0Semi standard non polar33892256
Astragalin,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C(C1=CC=C(O)C=C1)O24450.1Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14441.1Semi standard non polar33892256
Astragalin,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@H]1[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@@H](O)[C@@H]1O4431.9Semi standard non polar33892256
Astragalin,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@H]1O4419.2Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O4411.6Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4523.6Semi standard non polar33892256
Astragalin,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C14537.7Semi standard non polar33892256
Astragalin,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C14567.6Semi standard non polar33892256
Astragalin,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C14550.2Semi standard non polar33892256
Astragalin,2TBDMS,isomer #13CC(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](O)[C@H]1O)=C(C1=CC=C(O)C=C1)O24520.5Semi standard non polar33892256
Astragalin,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)=C(C1=CC=C(O)C=C1)O24518.6Semi standard non polar33892256
Astragalin,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC=C(O)C=C1)O24524.2Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14526.9Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14528.6Semi standard non polar33892256
Astragalin,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](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14534.5Semi standard non polar33892256
Astragalin,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)O[C@H]1[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@@H]1CO4509.1Semi standard non polar33892256
Astragalin,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4519.2Semi standard non polar33892256
Astragalin,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@H]1O4523.9Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@H]1O[Si](C)(C)C(C)(C)C4506.4Semi standard non polar33892256
Astragalin,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4502.9Semi standard non polar33892256
Astragalin,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4520.8Semi standard non polar33892256
Astragalin,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4500.4Semi standard non polar33892256
Astragalin,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4518.6Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14566.6Semi standard non polar33892256
Astragalin,2TBDMS,isomer #8CC(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](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14529.5Semi standard non polar33892256
Astragalin,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14529.9Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4657.2Semi standard non polar33892256
Astragalin,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O)[C@@H]1O4596.3Semi standard non polar33892256
Astragalin,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4573.7Semi standard non polar33892256
Astragalin,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4596.1Semi standard non polar33892256
Astragalin,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4607.8Semi standard non polar33892256
Astragalin,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4626.9Semi standard non polar33892256
Astragalin,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C4611.5Semi standard non polar33892256
Astragalin,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](O)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14662.4Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14669.0Semi standard non polar33892256
Astragalin,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](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C14657.5Semi standard non polar33892256
Astragalin,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C14758.3Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O[Si](C)(C)C(C)(C)C)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O4639.7Semi standard non polar33892256
Astragalin,3TBDMS,isomer #20CC(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](O[Si](C)(C)C(C)(C)C)[C@H]3O)=C(C3=CC=C(O)C=C3)OC2=C14604.2Semi standard non polar33892256
Astragalin,3TBDMS,isomer #21CC(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](O)[C@H]3O[Si](C)(C)C(C)(C)C)=C(C3=CC=C(O)C=C3)OC2=C14604.9Semi standard non polar33892256
Astragalin,3TBDMS,isomer #22CC(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](O)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C14670.4Semi standard non polar33892256
Astragalin,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C3)OC2=C14624.2Semi standard non polar33892256
Astragalin,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C14676.8Semi standard non polar33892256
Astragalin,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C3O2)C=C14670.7Semi standard non polar33892256
Astragalin,3TBDMS,isomer #26CC(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](O)[C@H]3O)C(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)C=C14658.2Semi standard non polar33892256
Astragalin,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C14663.3Semi standard non polar33892256
Astragalin,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC=C(C2=C(O[C@@H]3O[C@H](CO)[C@@H](O)[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=C14655.7Semi standard non polar33892256
Astragalin,3TBDMS,isomer #29CC(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](O[Si](C)(C)C(C)(C)C)[C@H]1O)=C(C1=CC=C(O)C=C1)O24590.4Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O4626.6Semi standard non polar33892256
Astragalin,3TBDMS,isomer #30CC(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](O)[C@H]1O[Si](C)(C)C(C)(C)C)=C(C1=CC=C(O)C=C1)O24587.8Semi standard non polar33892256
Astragalin,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C(O[C@@H]1O[C@H](CO)[C@@H](O)[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=C1)O24606.3Semi standard non polar33892256
Astragalin,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](O[Si](C)(C)C(C)(C)C)[C@H]3O)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14612.5Semi standard non polar33892256
Astragalin,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](O)[C@H]3O[Si](C)(C)C(C)(C)C)C(=O)C3=C(O)C=C(O)C=C3O2)C=C14613.6Semi standard non polar33892256
Astragalin,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](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=C14629.0Semi standard non polar33892256
Astragalin,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)[C@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O)=CC(O)=C3C2=O)O[C@H](CO)[C@H]1O[Si](C)(C)C(C)(C)C4595.0Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4607.8Semi standard non polar33892256
Astragalin,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=C3)OC3=CC(O)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4628.9Semi standard non polar33892256
Astragalin,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O)[C@@H]1O4635.5Semi standard non polar33892256
Astragalin,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)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](O)[C@@H]1O4616.7Semi standard non polar33892256
Astragalin,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O4588.1Semi standard non polar33892256
Astragalin,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC[C@H]1O[C@@H](OC2=C(C3=CC=C(O)C=C3)OC3=CC(O[Si](C)(C)C(C)(C)C)=CC(O)=C3C2=O)[C@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C4613.2Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Astragalin GC-MS (Non-derivatized) - 70eV, Positivesplash10-0f8i-8914600000-70416132b3766fd636fb2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Astragalin GC-MS (3 TMS) - 70eV, Positivesplash10-0f72-4730019000-7036585c066b67f1f0ce2017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Astragalin GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 10V, Negative-QTOFsplash10-0iki-0930000000-20176d350f94ae4a84ed2017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 20V, Negative-QTOFsplash10-0002-0020900000-182256be3fac5a878f1b2017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 30V, Negative-QTOFsplash10-001i-0090100000-7bd32a5c1969c5a248ac2017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 40V, Negative-QTOFsplash10-0560-0090000000-1c2e7f81b693e62971832017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 50V, Negative-QTOFsplash10-0a6r-0090000000-364026dfdcefd0d2e3a92017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF , Negative-QTOFsplash10-0002-0000900030-4139a6b8a2e916a0ea742017-08-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 10V, Negative-QTOFsplash10-0002-0000900000-b3cdd88343725a79c5e02017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 10V, Negative-QTOFsplash10-0002-0000900010-9834ce03ded5a1fe8c482017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 20V, Negative-QTOFsplash10-0002-0020900000-182256be3fac5a878f1b2017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 30V, Negative-QTOFsplash10-001i-0090100000-7bd32a5c1969c5a248ac2017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 40V, Negative-QTOFsplash10-0560-0090000000-1c2e7f81b693e62971832017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF 50V, Negative-QTOFsplash10-0a6r-0090000000-364026dfdcefd0d2e3a92017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin ESI-TOF , Negative-QTOFsplash10-0002-0000900030-4139a6b8a2e916a0ea742017-09-12HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin LC-ESI-QTOF , negative-QTOFsplash10-052b-0090400000-98b6bb6a62f4d8812fde2017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin LC-ESI-QTOF , negative-QTOFsplash10-0002-0020900010-4e6aa6edffb0c4b2f8322017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin LC-ESI-QTOF , negative-QTOFsplash10-0a59-0090000000-94e191a13790b3b499522017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin LC-ESI-QTOF , negative-QTOFsplash10-0002-0000900000-1c8fa629cb5881a429332017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin LC-ESI-QTOF , negative-QTOFsplash10-055b-0090200000-269c7f2460a6f35009c82017-09-14HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Astragalin LC-ESI-QTOF , negative-QTOFsplash10-0a7i-0090000000-d43f3a3dfafef985b9ef2017-09-14HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Astragalin 10V, Positive-QTOFsplash10-000j-0190800000-d3b297eb0fe481caa10a2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Astragalin 20V, Positive-QTOFsplash10-000i-0190000000-1e520254d0769f8f845e2016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Astragalin 40V, Positive-QTOFsplash10-05n0-3590000000-7f6360b543570fc557162016-06-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Astragalin 10V, Negative-QTOFsplash10-000b-1151900000-879fdf0c200d1a8caf5b2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Astragalin 20V, Negative-QTOFsplash10-000i-1190200000-8b8be60a1a225937d8d82016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Astragalin 40V, Negative-QTOFsplash10-000i-3590000000-22efe60043282fcdf3792016-08-03Wishart 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 ID319
FooDB IDFDB016478
KNApSAcK IDC00005138
Chemspider ID4445311
KEGG Compound IDC12249
BioCyc IDCPD1F-453
BiGG IDNot Available
Wikipedia LinkAstragalin
METLIN IDNot Available
PubChem Compound5282102
PDB IDNot Available
ChEBI ID30200
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1051431
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.. .