127761-61-9

Basic information

• Product Name: 3β-(2',3',4',6'-Tetra-O-acetyl-β-D-glucopyranosyloxy)-12β-acetoxydammar-24-en-20(S)-ol
• Synonyms: 3β-(2',3',4',6'-Tetra-O-acetyl-β-D-glucopyranosyloxy)-12β-acetoxydammar-24-en-20(S)-ol
• CAS NO: 127761-61-9
• Molecular Weight: 833.07
• Mol File: 127761-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3β-(2',3',4',6'-Tetra-O-acetyl-β-D-glucopyranosyloxy)-12β-acetoxydammar-24-en-20(S)-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 3β-(2',3',4',6'-Tetra-O-acetyl-β-D-glucopyranosyloxy)-12β-acetoxydammar-24-en-20(S)-ol(127761-61-9)
• EPA Substance Registry System: 3β-(2',3',4',6'-Tetra-O-acetyl-β-D-glucopyranosyloxy)-12β-acetoxydammar-24-en-20(S)-ol(127761-61-9)

Safety Data

• Hazardous Substances Data: 127761-61-9(Hazardous Substances Data)

Upstream product

• 108-24-7 acetic anhydride 
• 67400-17-3 ginsenoside Rh₂ 

Downstream Products

• 67400-17-3 ginsenoside Rh₂ 
• 67400-17-3 Ginsenoside R_h2 

Relevant articles and documents

Synthesis and anti-cancer cell activity of pseudo-ginsenoside Rh2

β-d-Glucopyranoside,(3β,12β,20E)-12,25-dihydroxydammar-20(22)-en-3-yl (pseudo-ginsenoside Rh2) and its 20Z-isomer were synthesized from ginsenoside Rh2 under a mild condition, via a simple three-step called acetylation, elimination-addition and saponification. In addition, their activities were evaluated by eight different human tumor cells, compared with ginsenoside Rh2 group. Results indicated that the reaction in the side chain might greatly enhance the anti-proliferative activity of ginsenosides.