Neu5Troc[1Me,4789Ac]α(2-3)Gal[26Bn]-β-MP
≥98%(HPLC)
- Product Code: 59186
CAS:
610763-72-9
| Molecular Weight: | 1073.31 g./mol | Molecular Formula: | C₄₈H₅₆Cl₃NO₂₀ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in glycobiology research for studying glycan interactions and cellular recognition processes. It serves as a synthetic glycan derivative, enabling scientists to investigate the role of sialic acid-containing structures in biological systems. Its modified structure, including protective groups like Troc and Bn, allows for controlled enzymatic or chemical transformations, making it valuable in the synthesis of complex oligosaccharides. It is particularly useful in probing the binding specificity of lectins, antibodies, or other glycan-binding proteins, aiding in the development of glycoconjugate vaccines or diagnostic tools. Additionally, its application extends to studying the role of glycosylation in cell signaling, pathogen-host interactions, and immune responses. The chemical’s design also supports the exploration of sialyltransferase activity and the development of glycosylation inhibitors for therapeutic purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿9,200.00 |
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| 1.000 | 10-20 days | ฿24,090.00 |
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Neu5Troc[1Me,4789Ac]α(2-3)Gal[26Bn]-β-MP
This chemical is primarily utilized in glycobiology research for studying glycan interactions and cellular recognition processes. It serves as a synthetic glycan derivative, enabling scientists to investigate the role of sialic acid-containing structures in biological systems. Its modified structure, including protective groups like Troc and Bn, allows for controlled enzymatic or chemical transformations, making it valuable in the synthesis of complex oligosaccharides. It is particularly useful in probing the binding specificity of lectins, antibodies, or other glycan-binding proteins, aiding in the development of glycoconjugate vaccines or diagnostic tools. Additionally, its application extends to studying the role of glycosylation in cell signaling, pathogen-host interactions, and immune responses. The chemical’s design also supports the exploration of sialyltransferase activity and the development of glycosylation inhibitors for therapeutic purposes.
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