ChemSpider 2D Image | kaempferol 3-O-alpha-L-arabinopyranosyl-7-O-alpha-L-rhamnopyranoside | C26H28O14

kaempferol 3-O-α-L-arabinopyranosyl-7-O-α-L-rhamnopyranoside

  • Molecular FormulaC26H28O14
  • Average mass564.492 Da
  • Monoisotopic mass564.147888 Da
  • ChemSpider ID28493004

  • defined stereocentres - 9 of 9 defined stereocentres

More details:

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

3-(α-L-Arabinopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl 6-deoxy-α-L-mannopyranoside [ACD/IUPAC Name]
3-(α-L-Arabinopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yl-6-desoxy-α-L-mannopyranosid [German] [ACD/IUPAC Name]
4H-1-Benzopyran-4-one, 3-(α-L-arabinopyranosyloxy)-7-[(6-deoxy-α-L-mannopyranosyl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)- [ACD/Index Name]
6-Désoxy-α-L-mannopyranoside de 3-(α-L-arabinopyranosyloxy)-5-hydroxy-2-(4-hydroxyphényl)-4-oxo-4H-chromén-7-yle [French] [ACD/IUPAC Name]
kaempferol 3-O-α-L-arabinopyranosyl-7-O-α-L-rhamnopyranoside
  • Miscellaneous

    • Chemical Class:

      A glycosyloxyflavone that is kaempferol attached to a <stereo>alpha</stereo>-<stereo>L</stereo>-arabinopyranosyl residue at position 3 and a <stereo>alpha</stereo>-<stereo>L</stereo>-rhamnopyranosyl r esidue at position 7 via glycosidic linkages. Isolated from the aerial parts of <ital>Vicia faba</ital> and <ital>Lotus edulis</ital>, it exhibits inhibitory activity against topoisomerase I and II. ChEBI CHEBI:68878
      A glycosyloxyflavone that is kaempferol attached to a alpha-L-arabinopyranosyl residue at position 3 and a alpha-L-rhamnopyranosyl r; esidue at position 7 via glycosidic linkages. Isolated from the a erial parts of Vicia faba and Lotus edulis, it exhibits inhibitory activity against topoisomerase I and II. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:68878
      A glycosyloxyflavone that is kaempferol attached to a alpha-L-arabinopyranosyl residue at position 3 and a alpha-L-rhamnopyranosyl residue at position 7 via glycosidic linkages. Isolated from the aer ial parts of Vicia faba and Lotus edulis, it exhibits inhibitory activity against topoisomerase I and II. ChEBI CHEBI:68878

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

Density: 1.7±0.1 g/cm3
Boiling Point: 917.5±65.0 °C at 760 mmHg
Vapour Pressure: 0.0±0.3 mmHg at 25°C
Enthalpy of Vaporization: 139.8±3.0 kJ/mol
Flash Point: 308.4±27.8 °C
Index of Refraction: 1.740
Molar Refractivity: 130.5±0.4 cm3
#H bond acceptors: 14
#H bond donors: 8
#Freely Rotating Bonds: 5
#Rule of 5 Violations: 3
ACD/LogP: 1.17
ACD/LogD (pH 5.5): -0.34
ACD/BCF (pH 5.5): 1.00
ACD/KOC (pH 5.5): 12.91
ACD/LogD (pH 7.4): -1.77
ACD/BCF (pH 7.4): 1.00
ACD/KOC (pH 7.4): 1.00
Polar Surface Area: 225 Å2
Polarizability: 51.7±0.5 10-24cm3
Surface Tension: 109.9±5.0 dyne/cm
Molar Volume: 323.6±5.0 cm3

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