773145-61-2

Upstream product

• 545-06-2 trichloroacetonitrile 
• 18311-29-0 octabenzoyl-D-maltose 
• 18311-30-3 2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1→4)-2,3,6-tri-O-benzoyl-α-D-glucopyranosyl bromide 

Downstream Products

• 1360822-64-5 C₉₀H₉₄O₂₂ 
• 1352548-84-5 3-O-[2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1→4)-2,3,6-tri-O-benzoyl-β-D-glucopyranosyl]tigogenin 
• 1144493-03-7 3-O-[2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1→4)-2,3,6-tri-O-benzoyl-β-D-glucopyranosyl]cholestan 
• 1352548-81-2 2α-acetoxy-3-O-[2,3,4,6-tetra-O-benzoyl-β-D-glucopyranosyl-(1→4)-2,3,6-tri-O-benzoyl-β-D-glucopyranosyl]cholestan 

Relevant academic research and scientific papers

Antifungal activity of 2α,3β-functionalized steroids stereoselectively increases with the addition of oligosaccharides

Invasive fungal infections pose a significant problem to the immune-compromised. Moreover, increased resistance to common antifungals requires development of novel compounds that can be used to treat invasive fungal infections. Naturally occurring steroid

Synthesis and hemolytic activity of some hederagenin diglycosides

Glycosylation of hederagenin with the trichloroacetimidate derivatives of six commercial disaccharides (D-cellobiose, D-lactose, D-maltose, D-melibiose, D-gentiobiose, D-isomaltose) was performed giving the protected saponins in high yields. Deprotection