Cas No.152488-28-3 Phenyl 4-O-acetyl-2,6-di-O-benzoyl-1-thio-β-thio-β-D-galactopyranoside

Thioglycosidic bonds are more stable than conventional oxyglycosidic bonds, especially in enzymatic degradation reactions where they are not easily hydrolyzed. Therefore, this compound can be used to synthesize sugar conjugates with enhanced stability. This is very useful for developing drug molecules or functional materials with specific biological activity and chemical stability. The structural modification of this compound makes it a key intermediate for the synthesis of complex carbohydrate drugs. By removing or converting protective groups, candidate molecules of glycosides with biological activity can be obtained, especially in the development of antiviral, anti-tumor, or antibacterial drugs.