The chemical substance known as D-Glucose, O-2-(acetylamino)-2-deoxy-b-D-galactopyranosyl-(1→3)-O-a-D-galactopyranosyl-(1→4)-O-b-D-galactopyranosyl-(1→4)-, with the CAS number 75660-79-6, is a complex carbohydrate that belongs to the category of glycosides. This compound features multiple sugar units linked through glycosidic bonds, specifically involving D-glucose and D-galactose moieties. The presence of an acetylamino group indicates that it has been modified, which can influence its solubility, reactivity, and biological activity. The structural configuration suggests that it may play a role in biological processes, potentially serving as a substrate for enzymes or as a component in cellular signaling pathways. Its intricate structure may also contribute to its function in various biochemical contexts, such as in cell recognition or as part of larger polysaccharides. Overall, this compound exemplifies the complexity and diversity of carbohydrate chemistry, highlighting the significance of glycosidic linkages in determining the properties and functions of sugar molecules.

D-Glucose,O-2-(acetylamino)-2-deoxy-b-D-galactopyranosyl-(1®3)-O-a-D-galactopyranosyl-(1®4)-O-b-D-galactopyranosyl-(1®4)-

75660-79-6: The chemical substance known as D-Glucose, O-2-(acetylamino)-2-deoxy-b-D-galactopyranosyl-(1→3)-O-a-D-galactopyranosyl-(1→4)-O-b-D-galactopyranosyl-(1→4)-, with the CAS number 75660-79-6, is a complex carbohydrate that belongs to the category of glycosides. This compound features multiple sugar units linked through glycosidic bonds, specifically involving D-glucose and D-galactose moieties. The presence of an acetylamino group indicates that it has been modified, which can influence its solubility, reactivity, and biological activity. The structural configuration suggests that it may play a role in biological processes, potentially serving as a substrate for enzymes or as a component in cellular signaling pathways. Its intricate structure may also contribute to its function in various biochemical contexts, such as in cell recognition or as part of larger polysaccharides. Overall, this compound exemplifies the complexity and diversity of carbohydrate chemistry, highlighting the significance of glycosidic linkages in determining the properties and functions of sugar molecules.

Globo-N-tetraose

<p>Tetrasaccharide associated with the glycolipid globoside</p>

CAS 75660-79-6

D-Glucose,O-2-(acetylamino)-2-deoxy-b-D-galactopyranosyl-(1®3)-O-a-D-galactopyranosyl-(1®4)-O-b-D-galactopyranosyl-(1®4)-

Globo-N-tetraose

Ref: 7W-GC3970

Globo-N-tetraose

Ref: 3D-OG06574