N-Fmoc-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl)-L-serine

≥98%

Reagent Code: #103845
label
Alias Fmoc-Ser[GalNAc(Ac)3-α-D]-OH
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CAS Number 120173-57-1

science Other reagents with same CAS 120173-57-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 656.63 g/mol
Formula C₃₂H₃₆N₂O₁₃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This chemical is primarily used in the synthesis of glycopeptides, which are important in studying biological processes and developing therapeutic agents. It serves as a protected glycosyl amino acid building block, enabling the incorporation of glycosylated serine residues into peptide chains. The Fmoc group provides protection during solid-phase peptide synthesis, while the acetyl groups shield the sugar moiety from unwanted reactions. This compound is particularly valuable in glycobiology research for creating glycopeptide mimics to investigate protein-carbohydrate interactions, immune responses, and cell signaling pathways. It is also utilized in the development of glycoconjugate vaccines and glycoprotein-based drugs, where precise glycosylation patterns are crucial for biological activity.

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Test Parameter Specification
Appearance White to light yellow and faint beige to beige and faint brown to light brown
Purity (%) 98-100%
1H NMR Spectrum Consistent With Structure
LCMS Consistent With Structure
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿2,110.00
inventory 25mg
10-20 days ฿5,620.00

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N-Fmoc-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl)-L-serine
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This chemical is primarily used in the synthesis of glycopeptides, which are important in studying biological processes and developing therapeutic agents. It serves as a protected glycosyl amino acid building block, enabling the incorporation of glycosylated serine residues into peptide chains. The Fmoc group provides protection during solid-phase peptide synthesis, while the acetyl groups shield the sugar moiety from unwanted reactions. This compound is particularly valuable in glycobiology research for creating glycopeptide mimics to investigate protein-carbohydrate interactions, immune responses, and cell signaling pathways. It is also utilized in the development of glycoconjugate vaccines and glycoprotein-based drugs, where precise glycosylation patterns are crucial for biological activity.
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