Neu5Gcα(2-6)Galβ MP Glycoside
≥97%
- Product Code: 103857
CAS:
1072896-38-8
Molecular Weight: | 593.54 g./mol | Molecular Formula: | C₂₄H₃₅NO₁₆ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in glycobiology research to study the interactions and roles of sialic acids in biological systems. It serves as a critical tool for investigating cell surface recognition processes, immune responses, and pathogen-host interactions. Researchers use it to synthesize and analyze glycoconjugates, enabling the exploration of how sialylated structures influence cellular communication and signaling. Additionally, it aids in the development of biomarkers and therapeutic targets for diseases where sialic acid metabolism is dysregulated, such as cancer and infectious diseases. Its application extends to the design of glycan-based vaccines and inhibitors, leveraging its structural mimicry of natural sialylated molecules.
Product Specification:
Test | Specification |
---|---|
Appearance | White To Almost White Powder To Crystal |
Purity (%) | 96.5-100 |
Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.005 | 10-20 days | ฿63,380.00 |
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Neu5Gcα(2-6)Galβ MP Glycoside
This compound is primarily utilized in glycobiology research to study the interactions and roles of sialic acids in biological systems. It serves as a critical tool for investigating cell surface recognition processes, immune responses, and pathogen-host interactions. Researchers use it to synthesize and analyze glycoconjugates, enabling the exploration of how sialylated structures influence cellular communication and signaling. Additionally, it aids in the development of biomarkers and therapeutic targets for diseases where sialic acid metabolism is dysregulated, such as cancer and infectious diseases. Its application extends to the design of glycan-based vaccines and inhibitors, leveraging its structural mimicry of natural sialylated molecules.
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