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Alyssonoside

Base Information
  • Chemical Name:Alyssonoside
  • CAS No.:142674-76-8
  • Molecular Formula:C35H46 O19
  • Molecular Weight:770.7283
  • Hs Code.:
Alyssonoside

Synonyms:alyssonoside;beta-(3,4-dihydroxyphenyl)ethyl-O-(alpha-L-rhamnopyranosyl-(1-3))-O-(beta-D-apiopyranosyl-(1-6))-4-feruloyl-beta-D-glucopyranoside

Suppliers and Price of Alyssonoside
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 2 raw suppliers
Chemical Property of Alyssonoside
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Boiling Point:1016.5°Cat760mmHg 
  • Flash Point:314°C 
  • PSA:293.21000 
  • Density:1.59g/cm3 
  • LogP:-2.24800 
  • XLogP3:-1.4
  • Hydrogen Bond Donor Count:10
  • Hydrogen Bond Acceptor Count:19
  • Rotatable Bond Count:15
  • Exact Mass:770.26332923
  • Heavy Atom Count:54
  • Complexity:1210
Purity/Quality:

85.0-99.8% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O
  • Isomeric SMILES:CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)/C=C/C3=CC(=C(C=C3)O)OC)COC4C(C(CO4)(CO)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O
Refernces

Phenylpropanoid glycosides from Lamiophlomis rotata

10.1016/S0031-9422(99)00027-8

The study focuses on the isolation and structural identification of two new phenylpropanoid glycosides, 6'-β-D-apiofuranosyl cistanoside C and cis-lamiophlomiside A, from the roots of Lamiophlomis rotata, a plant used in traditional Chinese medicine. The research utilized spectral and chemical evidence to determine the structures of the compounds, which were found to be similar to known compounds like lamiophlomiside A, alyssonoside, and forsythoside B. The study also involved the hydrolysis of compound 2, leading to the identification of its sugar components, and permethylation of compound 2 and lamiophlomiside A to confirm their structural similarities. The findings contribute to the understanding of the phytochemical constituents of L. rotata and their potential applications in medicine.

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