ChemSpider 2D Image | Salzmannianoside A | C47H74O17

Salzmannianoside A

  • Molecular FormulaC47H74O17
  • Average mass911.080 Da
  • Monoisotopic mass910.492615 Da
  • ChemSpider ID10236941

  • defined stereocentres - 23 of 23 defined stereocentres

More details:

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

(3β)-3-{[6-Deoxy-α-L-mannopyranosyl-(1->2)-[β-D-glucopyranosyl-(1->4)]-α-L-arabinopyranosyl]oxy}-23-oxoolean-12-en-28-oic acid [ACD/IUPAC Name]
(3β)-3-{[6-Desoxy-α-L-mannopyranosyl-(1->2)-[β-D-glucopyranosyl-(1->4)]-α-L-arabinopyranosyl]oxy}-23-oxoolean-12-en-28-säure [German] [ACD/IUPAC Name]
Acide (3β)-3-{[6-désoxy-α-L-mannopyranosyl-(1->2)-[β-D-glucopyranosyl-(1->4)]-α-L-arabinopyranosyl]oxy}-23-oxooléan-12-én-28-oïque [French] [ACD/IUPAC Name]
Olean-12-en-28-oic acid, 3-[[O-6-deoxy-α-L-mannopyranosyl-(1->2)-O-[β-D-glucopyranosyl-(1->4)]-α-L-arabinopyranosyl]oxy]-23-oxo-, (3β)- [ACD/Index Name]
Salzmannianoside A
3-O-{[β-D-glucopyranosyl-(1->4)]-[α-L-rhamnopyranosyl-(1->2)]-α-L-arabinopyranosyl}gypsogenin
  • Miscellaneous

    • Chemical Class:

      A triterpenoid saponin that consists of gypsogenin attached to a <stereo>alpha</stereo>-<stereo>L</stereo>-rhamnopyranosyl-(1<arrow>right</arrow>2)-[<stereo>beta</stereo>-<stereo>D</stereo>-glucopyran osyl-(1<arrow>right</arrow>4)]-<stereo>alpha</stereo>-<stereo>L</stereo>-arabinopyranosyl] residue at position 3 via a glycosidic linkage. Isolated from <ital>Serjania salzmanniana</ital>, it exhibits antifungal and molluscicidal activities. ChEBI CHEBI:66157
      A triterpenoid saponin that consists of gypsogenin attached to a alpha-L-rhamnopyranosyl-(1->2)-[beta-D-glucopyranosyl-(1->4)]-alpha-L-arabinopyranosyl] residue at position 3 via a glycosidic linkage. Isolated from Serjania salzmanniana, it exhibits antifungal and molluscicidal activities. ChEBI CHEBI:66157
      A triterpenoid saponin that consists of gypsogenin attached to a alpha-L-rhamnopyranosyl-(1right2)-[beta-D-glucopyran; osyl-(1right4)]-alpha-L-arabinopyranosyl] residue at position 3 via a glycosidic linkage. Isolated from Serjania salzmanniana, it exhibits; antifungal and molluscicidal activities. ChEBI https://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:66157

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

Density: 1.4±0.1 g/cm3
Boiling Point: 991.4±65.0 °C at 760 mmHg
Vapour Pressure: 0.0±0.6 mmHg at 25°C
Enthalpy of Vaporization: 163.8±6.0 kJ/mol
Flash Point: 283.9±27.8 °C
Index of Refraction: 1.615
Molar Refractivity: 227.4±0.4 cm3
#H bond acceptors: 17
#H bond donors: 9
#Freely Rotating Bonds: 9
#Rule of 5 Violations: 4
ACD/LogP: 6.03
ACD/LogD (pH 5.5): 3.52
ACD/BCF (pH 5.5): 166.44
ACD/KOC (pH 5.5): 734.72
ACD/LogD (pH 7.4): 1.72
ACD/BCF (pH 7.4): 2.62
ACD/KOC (pH 7.4): 11.56
Polar Surface Area: 272 Å2
Polarizability: 90.2±0.5 10-24cm3
Surface Tension: 71.0±5.0 dyne/cm
Molar Volume: 651.7±5.0 cm3

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