Uridine 5′-diphospho-N-acetylgalactosamine disodium salt
98%
- Product Code: 103923
CAS:
108320-87-2
Molecular Weight: | 651.3200000000001 g./mol | Molecular Formula: | C₁₇H₂₆N₃Na₂O₁₇P₂ |
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EC Number: | MDL Number: | MFCD00077894 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | −20°C |
Product Description:
This compound is widely used in biochemical research, particularly in studies involving glycosylation processes. It serves as a substrate for glycosyltransferases, enzymes that catalyze the transfer of sugar moieties to various acceptor molecules. This is crucial for understanding the biosynthesis of glycoproteins and glycolipids, which play significant roles in cell signaling, immune response, and cellular communication. Additionally, it is utilized in the synthesis of complex carbohydrates and in the development of glycoconjugate vaccines, where it helps in creating antigenic structures that elicit strong immune responses. Its application extends to the field of glycobiology, aiding in the exploration of carbohydrate-mediated biological interactions and the development of therapeutic agents targeting glycosylation-related diseases.
Product Specification:
Test | Specification |
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Appearance | White Powder |
Purity (%) | 97.5-100 |
Solubility | Clear Colorless Solution At 5Mg Plus 0.1Ml Of Water |
Water By Karl Fischer | < Or = 7% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.005 | 10-20 days | £92.73 |
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0.025 | 10-20 days | £257.83 |
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Uridine 5′-diphospho-N-acetylgalactosamine disodium salt
This compound is widely used in biochemical research, particularly in studies involving glycosylation processes. It serves as a substrate for glycosyltransferases, enzymes that catalyze the transfer of sugar moieties to various acceptor molecules. This is crucial for understanding the biosynthesis of glycoproteins and glycolipids, which play significant roles in cell signaling, immune response, and cellular communication. Additionally, it is utilized in the synthesis of complex carbohydrates and in the development of glycoconjugate vaccines, where it helps in creating antigenic structures that elicit strong immune responses. Its application extends to the field of glycobiology, aiding in the exploration of carbohydrate-mediated biological interactions and the development of therapeutic agents targeting glycosylation-related diseases.
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