908835-48-3

Upstream product

• 94715-74-9 O-(2-Acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-glucopyranosyl)trichloracetimidat 
• 303114-51-4 oleanolic acid benzyl ester 
• 908835-49-4 28-O-benzyl 3-O-[3′,4′,6′-tri-O-acetyl-2′-deoxy-2′-phthalimido-β-D-glucopyranosyl] oleanolic ester 
• 508-02-1 Oleanolic acid 
• 100-39-0 benzyl bromide 
• 1616703-76-4 28-O-benzyl-3-O-[3′,4′,6′-tri-O-acetyl-2′-deoxy-2′-(2″,2″,2″-trichloroethyloxycarbonylamino)-β-D-glucopyranosyl]oleanolic ester 
• 108-24-7 acetic anhydride 

Downstream Products

• 908835-50-7 10-(7-acetylamino-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy)-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-octadecahydro-2H-picene-4a-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Synthesis and evaluation of the anticancer activity of albiziabioside A and its analogues as apoptosis inducers against human melanoma cells

We have efficiently synthesized albiziabioside A (1) together with its six disaccharide analogues through a linear synthesis, and evaluated their cytotoxicity against six different skin cancer cells. All of the analogues showed weak cytotoxicity, with the

Synthesis and antitumor activity of two natural N-acetylglucosamine-bearing triterpenoid saponins: Lotoidoside D and E

Two natural triterpenoid saponins bearing N-acetylglucosamine, lotoidoside D and lotoidoside E, which had been available only from Glinus lotoides growing in Egyptian desert, were facilely synthesized from readily available oleanolic acid. Preliminary pha