Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

sasanquasaponin

Base Information
  • Chemical Name:sasanquasaponin
  • CAS No.:8047-15-2
  • Molecular Formula:C27H42O3
  • Molecular Weight:0
  • Hs Code.:
sasanquasaponin

Synonyms:Glycosides,sapogenin;Sapogenins, glycosides;Saponins;Saponosides;Tea Saponin;

Suppliers and Price of sasanquasaponin
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 173 raw suppliers
Chemical Property of sasanquasaponin
Chemical Property:
  • Appearance/Colour:Light yellow powder 
  • PSA:0.00000 
  • Density:1.015-1.020 g/mL at 20 °C (5% in H2O)(lit.)  
  • LogP:0.00000 
Purity/Quality:

85%, *data from raw suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes: Xi:Irritant;
     
  • Statements: R36/37:; 
  • Safety Statements: S26:; S37/39:; 
MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:
Refernces

Synthesis and biological activity of 22-deoxo-23-oxa analogues of saponin OSW-1

10.1021/jm101648h

The research aimed to synthesize and biologically evaluate 22-deoxo-23-oxa analogues of the saponin OSW-1, which is known for its potent cytotoxic properties against various cancer cells. The purpose was to develop simpler OSW-1 analogues that retain high and selective anticancer activity while being less toxic to normal cells, thus widening the therapeutic window. The study successfully synthesized a series of OSW-1 analogues and tested their ability to inhibit cancer cell proliferation and induce apoptosis. The analogues were found to be slightly less active than OSW-1 but demonstrated significantly less toxicity to normal human fibroblasts, suggesting a broader therapeutic window. Key chemicals used in the synthesis process included steroidal 16β,17R,22-triol as the starting material, various carboxylic acids for esterification, and protecting groups such as triethylsilyl and acetyl groups. The synthesized analogues were then screened against eight cancer cell lines and normal human fibroblasts, with the results indicating that the analogues could induce concentration- and time-dependent apoptosis in mammalian cancer cells with caspase-3 activation.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 8047-15-2