BO48979
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Catalog Number: | BO48979 |
Chemical Name: | O-6-Deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl-(1→4)-O-[N-acetyl-α-neuraminosyl-(2→3)]-O-β-D-galactopyranosyl-(1→4)-β-D-glucopyranose |
CAS Number: | 1015758-43-6 |
Molecular Formula: | C43H72N2O33 |
Molecular Weight: | 1145.0254 |
SMILES: | OC[C@H]1O[C@@H](O[C@H]2[C@@H](CO)O[C@H]([C@@H]([C@H]2O[C@@]2(C[C@H](O)[C@H]([C@@H](O2)[C@@H]([C@@H](CO)O)O)NC(=O)C)C(=O)O)O)O[C@@H]2[C@@H](CO)O[C@H]([C@@H]([C@H]2O)O)O)[C@@H]([C@H]([C@H]1O)O[C@@H]1O[C@H](CO)[C@@H]([C@@H]([C@H]1O[C@@H]1O[C@@H](C)[C@H]([C@H]([C@@H]1O)O)O)O)O)NC(=O)C |
The O-6-Deoxy-α-L-galactopyranosyl-(1→2)-O-β-D-galactopyranosyl-(1→3)-O-2-(acetylamino)-2-deoxy-β-D-galactopyranosyl-(1→4)-O-[N-acetyl-α-neuraminosyl-(2→3)]-O-β-D-galactopyranosyl-(1→4)-β-D-glucopyranose molecule plays a crucial role in chemical synthesis, particularly in the development of glycoconjugates. This complex structure contains multiple glycosidic linkages that are essential for mimicking the intricate sugar arrangements found in biological systems. By utilizing this compound in chemical synthesis, researchers can create novel glycoconjugates with specific carbohydrate structures, enabling the study of glycan-mediated interactions and functions in biological processes. Additionally, the presence of acetyl and amino groups in the molecule provides opportunities for further chemical modifications, offering versatility in designing glycoconjugates for various applications in medicinal chemistry, biomaterials, and glycobiology.