ChemSpider 2D Image | Kaempferol 3,7-diglucoside | C27H30O16

Kaempferol 3,7-diglucoside

  • Molecular FormulaC27H30O16
  • Average mass610.518 Da
  • Monoisotopic mass610.153381 Da
  • ChemSpider ID4884845
  • defined stereocentres - 10 of 10 defined stereocentres


More details:






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

25615-14-9 [RN]
3-(β-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl β-D-glucopyranoside [ACD/IUPAC Name]
3-(β-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl-β-D-glucopyranosid [German] [ACD/IUPAC Name]
4H-1-Benzopyran-4-one, 3,7-bis(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)- [ACD/Index Name]
Kaempferol 3,7-diglucoside
kaempferol 3,7-di-O-β-D-glucoside
kaempferol-3-O-β-D-glucopyranosyl-7-O-β-D-glucopyranoside
β-D-Glucopyranoside de 3-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphényl)-4-oxo-4H-chromén-7-yle [French] [ACD/IUPAC Name]
3-(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-7-yl β-D-glucopyranoside
3,7-bis(β-D-glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
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Validated by Experts, Validated by Users, Non-Validated, Removed by Users

1SL009I82F [DBID]
  • Miscellaneous
    • Chemical Class:

      A glycosyloxyflavone that is kaempferol having two <stereo>beta</stereo>-<stereo>D</stereo>-glucosyl residues attached at positions O-3 and O-7. ChEBI CHEBI:133224, CHEBI:67928
      A glycosyloxyflavone that is kaempferol having two beta-D-glucosyl residues attached at positions O-3 and O-7. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:133224
      A kaempferol <element>O</element>-glucoside that is kaempferol attached to <stereo>beta</stereo>-<stereo>D</stereo>-glucopyranosyl residues at position 3 and 7 via glycosidic linkages. Isolated from the aerial parts of <ital>Delphinium staphisagria</ital>, it exhibits trypanocidal activity. ChEBI CHEBI:133224, CHEBI:67928
      A kaempferol O-glucoside that is kaempferol attached to beta-D-glucopyranosyl residues at position 3 and 7 via glycosidic linkages. Isolated from ; the aerial parts of Delphinium staphisagria, it exh ibits trypanocidal activity. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:67928

Predicted data is generated using the ACD/Labs Percepta Platform - PhysChem Module

Density: 1.8±0.1 g/cm3
Boiling Point: 1007.4±65.0 °C at 760 mmHg
Vapour Pressure: 0.0±0.3 mmHg at 25°C
Enthalpy of Vaporization: 154.0±3.0 kJ/mol
Flash Point: 333.3±27.8 °C
Index of Refraction: 1.764
Molar Refractivity: 138.2±0.4 cm3
#H bond acceptors: 16
#H bond donors: 10
#Freely Rotating Bonds: 7
#Rule of 5 Violations: 3
ACD/LogP: -0.22
ACD/LogD (pH 5.5): -1.30
ACD/BCF (pH 5.5): 1.00
ACD/KOC (pH 5.5): 3.91
ACD/LogD (pH 7.4): -2.72
ACD/BCF (pH 7.4): 1.00
ACD/KOC (pH 7.4): 1.00
Polar Surface Area: 266 Å2
Polarizability: 54.8±0.5 10-24cm3
Surface Tension: 125.3±5.0 dyne/cm
Molar Volume: 334.6±5.0 cm3

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