| Chemical Name: | D-Glucose,O-(N-acetyl-a-neuraminosyl)-(2?3)-O-b-D-galactopyranosyl-(1?3)-O-[6-deoxy-a-L-galactopyranosyl-(1?4)]-2-(acetylamino)-2-deoxy- |
| CAS Number: | 92448-22-1 |
| Product Number: | AG00GWZO(AGN-PC-0VZLI5) |
| Synonyms: | |
| MDL No: | MFCD00214218 |
| Molecular Formula: | C31H52N2O23 |
| Molecular Weight: | 820.74418 |
Sialyl Lewis A is a key molecule in chemical synthesis, particularly in the field of glycoscience. This unique carbohydrate structure plays a crucial role in various biological processes and interactions, making it a valuable tool for researchers and chemists alike.In chemical synthesis, Sialyl Lewis A serves as a versatile building block for the creation of complex glycan structures. Its specific arrangement of sugars and sialic acid residues enables precise manipulation and modification, allowing for the synthesis of tailored glycans with varied functions and properties.By incorporating Sialyl Lewis A into synthetic pathways, chemists can mimic natural glycan structures, investigate carbohydrate-protein interactions, and develop novel glycoconjugates with potential applications in drug discovery, vaccine development, and biomaterials science. Its strategic placement within synthetic schemes facilitates the construction of biologically relevant carbohydrates with defined structures and functions.Furthermore, the ability to access Sialyl Lewis A through chemical synthesis provides researchers with a sustainable and scalable method for obtaining this important glycan motif. This not only enables the study of its biological roles and functions but also opens up possibilities for the creation of new glycan-based therapeutics and diagnostics.Overall, the application of Sialyl Lewis A in chemical synthesis offers a pathway to explore the intricate world of carbohydrate chemistry, paving the way for innovative research and advancements in various scientific disciplines.
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