ChemSpider 2D Image | 6-hydroxyluteolin 7-O-laminaribioside | C27H30O17

6-hydroxyluteolin 7-O-laminaribioside

  • Molecular FormulaC27H30O17
  • Average mass626.517 Da
  • Monoisotopic mass626.148315 Da
  • ChemSpider ID9745667
  • defined stereocentres - 10 of 10 defined stereocentres


More details:






Validated by Experts, Validated by Users, Non-Validated, Removed by Users

2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-4-oxo-4H-chromen-7-yl 3-O-β-D-glucopyranosyl-β-D-glucopyranoside [ACD/IUPAC Name]
2-(3,4-Dihydroxyphenyl)-5,6-dihydroxy-4-oxo-4H-chromen-7-yl-3-O-β-D-glucopyranosyl-β-D-glucopyranosid [German] [ACD/IUPAC Name]
2-(3,4-Dihydroxyphenyl)-7-[(3-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-5,6-dihydroxy-4H-1-benzopyran-4-one
3-O-β-D-Glucopyranosyl-β-D-glucopyranoside de 2-(3,4-dihydroxyphényl)-5,6-dihydroxy-4-oxo-4H-chromén-7-yle [French] [ACD/IUPAC Name]
4H-1-Benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-[(3-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-5,6-dihydroxy- [ACD/Index Name]
6-hydroxyluteolin 7-O-laminaribioside
865205-40-9 [RN]
5,6,3',4'-tetrahydroxyflavone-7-O-β-D-glucopyranosyl-(1->3)-β-D-glucopyranoside
https://www.ebi.ac.uk/chembl/compoundreportcard/CHEMBL498848/
  • Miscellaneous
    • Chemical Class:

      A glycosyloxyflavone that is 6-hydroxyluteolin attached to a <stereo>beta</stereo>-<stereo>D</stereo>-glucopyranosyl-(1<arrow>right</arrow>3)-<stereo>beta</stereo>-<stereo>D</stereo>-glucopyranosyl mo iety at position 7 via a glycosidic linkage. Isolated from <ital>Globularia cordifolia</ital> and <ital>Globularia alypum</ital>, it exhibits antioxidant activity. ChEBI CHEBI:66046
      A glycosyloxyflavone that is 6-hydroxyluteolin attached to a beta-D-glucopyranosyl-(1->3)-beta-D-glucopyranosyl moiety at position 7 via a glycosidic linkage. Isolated from Globularia cordifolia and G lobularia alypum, it exhibits antioxidant activity. ChEBI CHEBI:66046
      A glycosyloxyflavone that is 6-hydroxyluteolin attached to a beta-D-glucopyranosyl-(1right3)-beta-D-glucopyranosyl mo; iety at position 7 via a glycosidic linkage. Isolated from Globularia cordifolia and Globularia alypum, it exhibits antioxidant activity. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:66046

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module, version: 14.00

Density: 1.9±0.1 g/cm3
Boiling Point: 1067.2±65.0 °C at 760 mmHg
Vapour Pressure: 0.0±0.3 mmHg at 25°C
Enthalpy of Vaporization: 163.8±3.0 kJ/mol
Flash Point: 351.4±27.8 °C
Index of Refraction: 1.788
Molar Refractivity: 139.9±0.4 cm3
#H bond acceptors: 17
#H bond donors: 11
#Freely Rotating Bonds: 7
#Rule of 5 Violations: 3
ACD/LogP: -1.38
ACD/LogD (pH 5.5): -1.78
ACD/BCF (pH 5.5): 1.00
ACD/KOC (pH 5.5): 2.20
ACD/LogD (pH 7.4): -3.14
ACD/BCF (pH 7.4): 1.00
ACD/KOC (pH 7.4): 1.00
Polar Surface Area: 286 Å2
Polarizability: 55.5±0.5 10-24cm3
Surface Tension: 139.1±5.0 dyne/cm
Molar Volume: 331.0±5.0 cm3

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