N-Fmoc-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-galactopyranosyl)-L-serine
≥98%
- Product Code: 103845
Alias:
Fmoc-Ser[GalNAc(Ac)3-α-D]-OH
CAS:
120173-57-1
| Molecular Weight: | 656.63 g./mol | Molecular Formula: | C₃₂H₃₆N₂O₁₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20℃ |
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.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Light Yellow And Faint Beige To Beige And Faint Brown To Light Brown |
| Purity (%) | 98-100 |
| 1 H NMR Spectrum | Consistent With Structure |
| LCMS | Consistent With Structure |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | ฿2,110.00 |
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| 0.025 | 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
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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