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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 23:47:16 UTC
Update Date2022-03-07 02:55:47 UTC
HMDB IDHMDB0038468
Secondary Accession Numbers
  • HMDB38468
Metabolite Identification
Common NameLuteolin 4'-glucoside
DescriptionLuteolin 4'-glucoside belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone. Luteolin 4'-glucoside has been detected, but not quantified in, pears (Pyrus communis). This could make luteolin 4'-glucoside a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on Luteolin 4'-glucoside.
Structure
Data?1563863202
Synonyms
ValueSource
(-)-Luteolin 4'-O-beta-glucosideHMDB
Juncein?HMDB
Luteolin 4'-O-beta-glucosideHMDB
Luteolin 4'-O-glucosideHMDB, MeSH
Chemical FormulaC21H20O11
Average Molecular Weight448.3769
Monoisotopic Molecular Weight448.100561482
IUPAC Name5,7-dihydroxy-2-(3-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)-4H-chromen-4-one
Traditional Name5,7-dihydroxy-2-(3-hydroxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)chromen-4-one
CAS Registry Number6920-38-3
SMILES
OCC1OC(OC2=C(O)C=C(C=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)C(O)C(O)C1O
InChI Identifier
InChI=1S/C21H20O11/c22-7-16-18(27)19(28)20(29)21(32-16)31-13-2-1-8(3-10(13)24)14-6-12(26)17-11(25)4-9(23)5-15(17)30-14/h1-6,16,18-25,27-29H,7H2
InChI KeyUHNXUSWGOJMEFO-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as flavonoid o-glycosides. Flavonoid O-glycosides are compounds containing a carbohydrate moiety which is O-glycosidically linked to the 2-phenylchromen-4-one flavonoid backbone.
KingdomOrganic compounds
Super ClassPhenylpropanoids and polyketides
ClassFlavonoids
Sub ClassFlavonoid glycosides
Direct ParentFlavonoid O-glycosides
Alternative Parents
Substituents
  • Flavonoid-4p-o-glycoside
  • Flavonoid o-glycoside
  • 3'-hydroxyflavonoid
  • 5-hydroxyflavonoid
  • 7-hydroxyflavonoid
  • Flavone
  • Hydroxyflavonoid
  • Phenolic glycoside
  • Hexose monosaccharide
  • Chromone
  • Glycosyl compound
  • O-glycosyl compound
  • Benzopyran
  • 1-benzopyran
  • Phenoxy compound
  • Phenol ether
  • Pyranone
  • Phenol
  • 1-hydroxy-4-unsubstituted benzenoid
  • 1-hydroxy-2-unsubstituted benzenoid
  • Pyran
  • Oxane
  • Monosaccharide
  • Benzenoid
  • Monocyclic benzene moiety
  • Vinylogous acid
  • Heteroaromatic compound
  • Secondary alcohol
  • Polyol
  • Acetal
  • Organoheterocyclic compound
  • Oxacycle
  • Organooxygen compound
  • Alcohol
  • Organic oxygen compound
  • Organic oxide
  • Hydrocarbon derivative
  • Primary alcohol
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
ProcessNot Available
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point178 - 179 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility1.02 g/LALOGPS
logP0.56ALOGPS
logP0.14ChemAxon
logS-2.6ALOGPS
pKa (Strongest Acidic)6.64ChemAxon
pKa (Strongest Basic)-3ChemAxon
Physiological Charge-1ChemAxon
Hydrogen Acceptor Count11ChemAxon
Hydrogen Donor Count7ChemAxon
Polar Surface Area186.37 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity107.04 m³·mol⁻¹ChemAxon
Polarizability43.19 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]+202.27830932474
DeepCCS[M-H]-199.88330932474
DeepCCS[M-2H]-232.83130932474
DeepCCS[M+Na]+208.19130932474
AllCCS[M+H]+202.832859911
AllCCS[M+H-H2O]+200.432859911
AllCCS[M+NH4]+205.032859911
AllCCS[M+Na]+205.632859911
AllCCS[M-H]-199.332859911
AllCCS[M+Na-2H]-199.732859911
AllCCS[M+HCOO]-200.332859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Luteolin 4'-glucosideOCC1OC(OC2=C(O)C=C(C=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)C(O)C(O)C1O5751.1Standard polar33892256
Luteolin 4'-glucosideOCC1OC(OC2=C(O)C=C(C=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)C(O)C(O)C1O4346.1Standard non polar33892256
Luteolin 4'-glucosideOCC1OC(OC2=C(O)C=C(C=C2)C2=CC(=O)C3=C(O)C=C(O)C=C3O2)C(O)C(O)C1O4529.1Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Luteolin 4'-glucoside,1TMS,isomer #1C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O4519.2Semi standard non polar33892256
Luteolin 4'-glucoside,1TMS,isomer #2C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O4484.3Semi standard non polar33892256
Luteolin 4'-glucoside,1TMS,isomer #3C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O)C3O)C(O)=C1)O24499.3Semi standard non polar33892256
Luteolin 4'-glucoside,1TMS,isomer #4C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O)=C3)OC2=C14594.5Semi standard non polar33892256
Luteolin 4'-glucoside,1TMS,isomer #5C[Si](C)(C)OC1C(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)OC(CO)C(O)C1O4545.0Semi standard non polar33892256
Luteolin 4'-glucoside,1TMS,isomer #6C[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C1O4551.6Semi standard non polar33892256
Luteolin 4'-glucoside,1TMS,isomer #7C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C1O4544.1Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #1C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O4408.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #10C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O4388.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #11C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C4403.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #12C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O)=C3)OC2=C14429.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #13C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O)C(O)=C1)O24399.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #14C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O)C(O)=C1)O24379.0Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #15C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C)C(O)=C1)O24411.7Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #16C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3)OC2=C14442.9Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #17C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3)OC2=C14430.9Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #18C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3)OC2=C14451.1Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #19C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C1O4432.8Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #2C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O4454.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #20C[Si](C)(C)OC1C(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)OC(CO)C(O)C1O[Si](C)(C)C4437.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #21C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C1O[Si](C)(C)C4415.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #3C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O4385.2Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #4C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O4432.5Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #5C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O4430.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #6C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C4419.3Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #7C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O4391.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #8C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3)OC2=C14436.2Semi standard non polar33892256
Luteolin 4'-glucoside,2TMS,isomer #9C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O4394.0Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #1C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O4255.3Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #10C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4272.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #11C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4247.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #12C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4257.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #13C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4314.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #14C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4328.9Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #15C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4297.0Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #16C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C)=C3)OC2=C14256.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #17C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O4229.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #18C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O4189.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #19C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C4237.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #2C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O4218.6Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #20C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3)OC2=C14275.2Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #21C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3)OC2=C14247.0Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #22C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14282.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #23C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4249.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #24C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4273.9Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #25C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4278.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #26C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O)=C3)OC2=C14253.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #27C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O)=C3)OC2=C14254.3Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #28C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O)=C3)OC2=C14244.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #29C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O)C(O)=C1)O24218.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #3C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O4267.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #30C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O)C3O[Si](C)(C)C)C(O)=C1)O24250.2Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #31C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)=C1)O24245.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #32C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3)OC2=C14261.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #33C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3)OC2=C14289.9Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #34C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3)OC2=C14293.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #35C[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4320.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #4C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O4224.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #5C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C4255.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #6C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O4259.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #7C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O4304.6Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #8C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O4275.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TMS,isomer #9C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C4293.6Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #1C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O4108.4Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #10C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4130.2Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #11C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4169.9Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #12C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4126.3Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #13C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4159.0Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #14C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4178.5Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #15C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4214.7Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #16C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4173.4Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #17C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4178.7Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #18C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4204.4Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #19C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4172.6Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #2C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O4145.1Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #20C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4250.5Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #21C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O)C(O[Si](C)(C)C)=C3)OC2=C14137.9Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #22C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3)OC2=C14130.8Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #23C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14128.3Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #24C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4090.6Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #25C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4115.4Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #26C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4104.2Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #27C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3)OC2=C14144.3Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #28C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14167.0Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #29C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14159.5Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #3C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O4160.2Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #30C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4180.9Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #31C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O)=C3)OC2=C14139.1Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #32C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O)=C3)OC2=C14146.1Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #33C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3)OC2=C14149.6Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #34C[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C3O[Si](C)(C)C)C(O)=C1)O24137.5Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #35C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3)OC2=C14179.1Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #4C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C4147.7Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #5C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4124.0Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #6C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4065.7Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #7C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4108.9Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #8C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4137.5Semi standard non polar33892256
Luteolin 4'-glucoside,4TMS,isomer #9C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4178.6Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #1C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O4077.1Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #10C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4127.9Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #11C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4111.7Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #12C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4130.9Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #13C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4106.3Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #14C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4168.6Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #15C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4172.5Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #16C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O)C(O[Si](C)(C)C)=C3)OC2=C14059.3Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #17C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14089.1Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #18C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14071.7Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #19C[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4056.5Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #2C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O4075.0Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #20C[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14109.7Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #21C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O)=C3)OC2=C14086.7Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #3C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O)C1O[Si](C)(C)C4068.1Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #4C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4103.2Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #5C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4125.9Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #6C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4099.1Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #7C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4060.2Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #8C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4080.5Semi standard non polar33892256
Luteolin 4'-glucoside,5TMS,isomer #9C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4056.4Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #1C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O4049.1Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #2C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O)C1O[Si](C)(C)C4054.9Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #3C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O)C(O[Si](C)(C)C)C1O[Si](C)(C)C4045.6Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #4C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O[Si](C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4074.8Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #5C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4065.8Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #6C[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C)C=C4O3)C=C2O[Si](C)(C)C)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C1O[Si](C)(C)C4105.3Semi standard non polar33892256
Luteolin 4'-glucoside,6TMS,isomer #7C[Si](C)(C)OC1=CC(O[Si](C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C)C(O[Si](C)(C)C)C4O[Si](C)(C)C)C(O[Si](C)(C)C)=C3)OC2=C14034.7Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O4791.1Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O4745.4Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O)C3O)C(O)=C1)O24751.1Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O)=C3)OC2=C14815.5Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)OC(CO)C(O)C1O4832.3Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OC1C(O)C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C1O4831.0Semi standard non polar33892256
Luteolin 4'-glucoside,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C1O4830.9Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O4860.9Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4850.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4856.3Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O)=C3)OC2=C14881.0Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O)C(O)=C1)O24856.3Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)=C1)O24860.1Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)=C1)O24857.3Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3)OC2=C14925.1Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3)OC2=C14930.2Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14927.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C1O4937.2Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O4921.4Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1C(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)OC(CO)C(O)C1O[Si](C)(C)C(C)(C)C4949.3Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C1O[Si](C)(C)C(C)(C)C4909.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4855.6Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4934.3Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4938.2Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4922.0Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O4816.8Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14887.2Semi standard non polar33892256
Luteolin 4'-glucoside,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4852.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #1CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C(C)(C)C)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O4963.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #10CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4900.2Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #11CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C(C)(C)C)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4903.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #12CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4891.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #13CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4952.6Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #14CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4974.2Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #15CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4949.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #16CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14952.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #17CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4869.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #18CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4858.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #19CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4864.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #2CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4O3)C=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4868.6Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #20CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14940.0Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #21CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14937.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #22CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)=C3)OC2=C14935.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #23CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C1O4879.3Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #24CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C1O[Si](C)(C)C(C)(C)C4902.2Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #25CC(C)(C)[Si](C)(C)OC1=CC(C2=CC(=O)C3=C(O)C=C(O)C=C3O2)=CC=C1OC1OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4903.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #26CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O)C(O)=C3)OC2=C14977.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #27CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3)OC2=C14996.5Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #28CC(C)(C)[Si](C)(C)OC1=CC(O[Si](C)(C)C(C)(C)C)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14950.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #29CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C3O)C(O)=C1)O24900.9Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #3CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4894.0Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #30CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C3O[Si](C)(C)C(C)(C)C)C(O)=C1)O24914.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #31CC(C)(C)[Si](C)(C)OC1=CC(O)=CC2=C1C(=O)C=C(C1=CC=C(OC3OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C3O[Si](C)(C)C(C)(C)C)C(O)=C1)O24916.4Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #32CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O[Si](C)(C)C(C)(C)C)C4O)C(O)=C3)OC2=C14958.7Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #33CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O[Si](C)(C)C(C)(C)C)C(O)C4O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14976.6Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #34CC(C)(C)[Si](C)(C)OC1=CC(O)=C2C(=O)C=C(C3=CC=C(OC4OC(CO)C(O)C(O[Si](C)(C)C(C)(C)C)C4O[Si](C)(C)C(C)(C)C)C(O)=C3)OC2=C14982.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #35CC(C)(C)[Si](C)(C)OC1C(CO)OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C1O[Si](C)(C)C(C)(C)C4957.1Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #4CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4908.8Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #5CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O[Si](C)(C)C(C)(C)C)C=C(O)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4892.6Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #6CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)C=C2O[Si](C)(C)C(C)(C)C)C(O)C(O)C1O4940.3Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #7CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)C=C2O)C(O[Si](C)(C)C(C)(C)C)C(O)C1O4956.9Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #8CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)C=C2O)C(O)C(O[Si](C)(C)C(C)(C)C)C1O4981.0Semi standard non polar33892256
Luteolin 4'-glucoside,3TBDMS,isomer #9CC(C)(C)[Si](C)(C)OCC1OC(OC2=CC=C(C3=CC(=O)C4=C(O)C=C(O[Si](C)(C)C(C)(C)C)C=C4O3)C=C2O)C(O)C(O)C1O[Si](C)(C)C(C)(C)C4956.3Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (Non-derivatized) - 70eV, Positivesplash10-001i-8934600000-c8e4d33f9553175fe3bb2017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (3 TMS) - 70eV, Positivesplash10-0f92-3363159000-f67408f361bb0512cb152017-10-06Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (Non-derivatized) - 70eV, PositiveNot Available2021-10-12Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Luteolin 4'-glucoside GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-11-04Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-001i-0920000000-3d3baf578d319bd2776a2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Negative-QTOFsplash10-000i-0090100000-6f49d81216936d8b55a92021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-001i-0920000000-30158851ea6bb0efb8ab2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000j-0090500000-665f19757855b18ca9152021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000i-0090200000-c77123c94eb48f949cc22021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000i-0090000000-9591033be6d3fb72fa882021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000j-0090400000-348aa5e019fb43587b7a2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-001i-0910000000-feb6d6b3858619587da92021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000i-0090000000-ad7e50e1d15ce9418f352021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000i-0090000000-94520eb801456854823b2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000i-0090000000-b003696371443919aa6a2021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000j-0090400000-cea122cba8dfcbe90f332021-09-20HMDB team, MONAView Spectrum
Experimental LC-MS/MSLC-MS/MS Spectrum - Luteolin 4'-glucoside 6V, Positive-QTOFsplash10-000i-0090000000-e81e47829a68440930072021-09-20HMDB team, MONAView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 10V, Positive-QTOFsplash10-000j-0190700000-1578c227b41df380d9c12015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 20V, Positive-QTOFsplash10-000i-0190100000-3b6efbaa6b7ca2cd995a2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 40V, Positive-QTOFsplash10-05n0-2790000000-5962588cabe4c28a4f0b2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 10V, Positive-QTOFsplash10-000j-0190700000-1578c227b41df380d9c12015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 20V, Positive-QTOFsplash10-000i-0190100000-3b6efbaa6b7ca2cd995a2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 40V, Positive-QTOFsplash10-05n0-2790000000-5962588cabe4c28a4f0b2015-04-24Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 10V, Negative-QTOFsplash10-000b-0151900000-d37b85771ce55bd22b782015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 20V, Negative-QTOFsplash10-000i-1090200000-e25cf79ee7db2464c3682015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 40V, Negative-QTOFsplash10-000l-2390000000-a7b4978a7079e2429df42015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 10V, Negative-QTOFsplash10-000b-0151900000-d37b85771ce55bd22b782015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 20V, Negative-QTOFsplash10-000i-1090200000-e25cf79ee7db2464c3682015-04-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Luteolin 4'-glucoside 40V, Negative-QTOFsplash10-000l-2390000000-a7b4978a7079e2429df42015-04-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB017827
KNApSAcK IDC00004276
Chemspider ID11446810
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound12304737
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .

Enzymes

General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:
UGT1A1
Uniprot ID:
P22309
Molecular weight:
59590.91
Reactions
Luteolin 4'-glucoside → Luteolin 4'-glucoside 7-galacturonidedetails