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![Molecular structure of 2-Acetamido-2-deoxy-N-[N-(benzyloxycarbonyl)-ε-aminocaproyl]-β-D-glucopyranosylamine, CAS Number: 56146-89-5 2-Acetamido-2-deoxy-N-[N-(benzyloxycarbonyl)-ε-aminocaproyl]-β-D-glucopyranosylamine (CAS 56146-89-5) - chemical structure im](https://media.scbt.com/product/2-acetamido-2-deoxy-n-n-benzyloxycarbonyl-epsilon-aminocaproyl-beta-d-glucopyranosylamine-56146-89-5-structure_08_27_t_82716.jpg)
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2-Acetamido-2-deoxy-N-[N-(benzyloxycarbonyl)-ε-aminocaproyl]-β-D-glucopyranosylamine is a chemically synthesized glycosylated compound designed for advanced research in carbohydrate chemistry and peptide-glycoconjugate synthesis. This molecule incorporates a unique structural arrangement by linking an amino acid derivative with a glucopyranosyl group through a specialized linkage, making it particularly useful for studying the interface between carbohydrates and proteins. In research, this compound serves as a crucial tool for investigating the specificity and mechanism of glycosyltransferases, which are enzymes involved in the attachment of sugars to proteins and other organic molecules. The presence of the benzyloxycarbonyl (Cbz) protective group on the amino function of the caproyl moiety allows researchers to explore the stepwise construction and deprotection of glycopeptides, which are of significant interest for understanding glycoprotein biosynthesis and function. Additionally, this compound aids in the synthesis of more complex glycostructures, pivotal for probing the biological roles of glycosylation in modulating protein stability, recognition, and signaling in cellular processes. Through such studies, insights into the enzymatic processes governing carbohydrate-protein conjugation are deepened, enhancing our understanding of cellular communication pathways and molecular recognition.
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
2-Acetamido-2-deoxy-N-[N-(benzyloxycarbonyl)-ε-aminocaproyl]-β-D-glucopyranosylamine, 10 mg | sc-223344 | 10 mg | $320.00 |