119742-55-1

Basic information

• Product Name: Olean-12-en-28-oicacid, 23-hydroxy-3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b,4a)-
• Synonyms: SieboldianosideA
• CAS NO: 119742-55-1
• Molecular Formula: C64H104 O30
• Molecular Weight: 1353.51
• Mol File: 119742-55-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Olean-12-en-28-oicacid, 23-hydroxy-3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b,4a)-(CAS DataBase Reference)
• NIST Chemistry Reference: Olean-12-en-28-oicacid, 23-hydroxy-3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b,4a)-(119742-55-1)
• EPA Substance Registry System: Olean-12-en-28-oicacid, 23-hydroxy-3-[(O-b-D-xylopyranosyl-(1®3)-O-6-deoxy-a-L-mannopyranosyl-(1®2)-a-L-arabinopyranosyl)oxy]-,O-6-deoxy-a-L-mannopyranosyl-(1®4)-O-b-D-glucopyranosyl-(1®6)-b-D-glucopyranosyl ester, (3b,4a)-(119742-55-1)

Safety Data

• Hazardous Substances Data: 119742-55-1(Hazardous Substances Data)

Downstream Products

• 465-99-6 hedaragenin 
• 17184-21-3 prosapogenin 
• 29321-28-6 sapindoside B 
• 27013-91-8 alpha-Hederin 
• 109606-00-0 methyl α-L-rhamnopyranosyl-1-4-β-D-glucopyranosyl-1-6-(α and β)-D-glucopyranoside 
• 75799-17-6 C₄₆H₇₄O₁₅ 

Relevant articles and documents

Metabolism of kalopanaxsaponin K by human intestinal bacteria and antirheumatoid arthritis activity of their metabolites.

When kalopanaxsaponin K (KPK) from Kalopanax pictus was incubated for 24 h at 37 degrees C with human intestinal microflora, KPK was mainly metabolized to kalopanaxsaponin I (KPI) via kalopanaxsaponin H (KPH) rather than via kalopanaxsaponin J (KPJ), and then transformed to kalopanaxsaponin A (KPA) and hederagenin. Bacteroides sp., and Bifidobacterium sp. and Fusobacterium sp. transformed KPK to KPI and KPA and hederagenin via KPH or KPJ. However, Lactobacillus sp. and Streptococcus sp. transformed KPK to KPI, KPA, and hederagenin only via KPJ. The metabolite KPA of KPK showed potent antirheumatoid arthritis activity.