3-O-(2,3,4,6-Tetra-O-acetyl-b-D-galactopyranosyl)-2-azido-4,6-O-benzylidene-2-deoxy-a-D-galactopyranosyl-Fmoc serine tert-butyl ester

95%

Reagent Code: #221146
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CAS Number 1477460-73-3

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Weight 988.99 g/mol
Formula C₄₉H₅₆N₄O₁₈
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in the synthesis of complex oligosaccharides and glycoconjugates, particularly in the development of glycoproteins and glycolipids for research in immunology and cancer biology. Serves as a glycosyl donor in solid-phase peptide synthesis, enabling site-specific glycosylation of serine residues. The presence of the Fmoc group allows for orthogonal protection in stepwise assembly, while the acetyl and benzylidene groups stabilize the sugar moiety during coupling reactions. Commonly applied in the preparation of antigenic mimics and vaccine candidates targeting carbohydrate-binding receptors.

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inventory 50mg
10-20 days ฿76,880.00

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3-O-(2,3,4,6-Tetra-O-acetyl-b-D-galactopyranosyl)-2-azido-4,6-O-benzylidene-2-deoxy-a-D-galactopyranosyl-Fmoc serine tert-butyl ester
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Used in the synthesis of complex oligosaccharides and glycoconjugates, particularly in the development of glycoproteins and glycolipids for research in immunology and cancer biology. Serves as a glycosyl donor in solid-phase peptide synthesis, enabling site-specific glycosylation of serine residues. The presence of the Fmoc group allows for orthogonal protection in stepwise assembly, while the acetyl and benzylidene groups stabilize the sugar moiety during coupling reactions. Commonly applied in the prepara
Used in the synthesis of complex oligosaccharides and glycoconjugates, particularly in the development of glycoproteins and glycolipids for research in immunology and cancer biology. Serves as a glycosyl donor in solid-phase peptide synthesis, enabling site-specific glycosylation of serine residues. The presence of the Fmoc group allows for orthogonal protection in stepwise assembly, while the acetyl and benzylidene groups stabilize the sugar moiety during coupling reactions. Commonly applied in the preparation of antigenic mimics and vaccine candidates targeting carbohydrate-binding receptors.
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