The chemical substance known as D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-[N-acetyl-α-neuraminosyl-(2→6)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-, with the CAS number 89458-13-9, is a complex glycosylated compound. It is characterized by its intricate structure, which includes multiple sugar units linked through glycosidic bonds, indicating its role in biological systems, particularly in cell recognition and signaling. The presence of N-acetyl-neuraminic acid suggests its involvement in sialylation processes, which are crucial for various physiological functions. This compound is likely to exhibit solubility in water due to its multiple hydroxyl groups, and it may participate in hydrogen bonding, influencing its interactions with other biomolecules. Its structural complexity may also confer specific biological activities, making it of interest in fields such as biochemistry and pharmacology. Overall, this substance exemplifies the diversity and functionality of carbohydrates in biological systems.

D-Glucose, O-6-deoxy-a-L-galactopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-O-[N-acetyl-a-neuraminosyl-(2®6)]-O-2-(acetylamino)-2-deoxy-b-D-glucopyranosyl-(1®3)-O-b-D-galactopyranosyl-(1®4)-

89458-13-9: The chemical substance known as D-Glucose, O-6-deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-[N-acetyl-α-neuraminosyl-(2→6)]-O-2-(acetylamino)-2-deoxy-β-D-glucopyranosyl-(1→3)-O-β-D-galactopyranosyl-(1→4)-, with the CAS number 89458-13-9, is a complex glycosylated compound. It is characterized by its intricate structure, which includes multiple sugar units linked through glycosidic bonds, indicating its role in biological systems, particularly in cell recognition and signaling. The presence of N-acetyl-neuraminic acid suggests its involvement in sialylation processes, which are crucial for various physiological functions. This compound is likely to exhibit solubility in water due to its multiple hydroxyl groups, and it may participate in hydrogen bonding, influencing its interactions with other biomolecules. Its structural complexity may also confer specific biological activities, making it of interest in fields such as biochemistry and pharmacology. Overall, this substance exemplifies the diversity and functionality of carbohydrates in biological systems.

<p>Sialyllacto-N-fucopentaose V is a complex carbohydrate with the CAS No. 89458-13-9. The molecular weight of this compound is 597.07 g/mol, and it has the following chemical structure:</p>

CAS 89458-13-9

D-Glucose, O-6-deoxy-a-L-galactopyranosyl-(1®2)-O-b-D-galactopyranosyl-(1®3)-O-[N-acetyl-a-neuraminosyl-(2®6)]-O-2-(acetylamino)-2-deoxy-b-D-glucopyranosyl-(1®3)-O-b-D-galactopyranosyl-(1®4)-

Sialyllacto-N-fucopentaose V

Ref: 3D-OS03891