495390-57-3

Upstream product

• 495390-51-7 2-[2-(2-chloroethoxy)ethoxy]ethyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside 
• 183901-63-5 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl trichloroacetimidate 
• 5197-62-6 2-[2-(chloroethoxy)ethoxy]ethanol 
• 495390-55-1 2-[2-(2-azidoethoxy)ethoxy]ethyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranoside 

Downstream Products

• 495390-58-4 C₄₇H₅₁NO₁₅ 
• 1356842-43-7 C₄₉H₅₁N₃O₁₃ 

Relevant academic research and scientific papers

Degradation of target oligosaccharides by anthraquinone-lectin hybrids with light switching

Anthraquinone-lectin hybrids were effectively synthesized using water-soluble anthraquinone derivative 11 with concanavalin A (ConA) and hygrophorus russula lectin (HRL) to give anthraquinone-ConA (16) and anthraquinone-HRL (17) hybrids, respectively. These anthraquinone-lectin hybrids effectively and selectively degraded oligosaccharides containing a mannose residue as a non-reducing terminal sugar, which has affinity for ConA and HRL, under photo-irradiation with long-wavelength UV light without additives and under neutral conditions. In addition, anthraquinone-HRL (17) selectively photo-degraded only Man(α1,6)Man, which has a high affinity for HRL, among several mannosides by recognition of both the type and glycosidic linkage profile of the sugar in an oligosaccharide.

New mannotriosides and trimannosides as potential ligands for mannose-specific binding proteins

The α-D-mannopyranosyl and 3,6-di-O-(α-D-mannopyranosyl)-α-D-mannopyranosyl neoglycolipids 3-6 and the branched and cluster trimannosidic acids 38 and 41 have been made in connection with studies of liposomes as transporters of antigens to dendritic cells