4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside
≥98%
- Product Code: 103744
Alias:
(2R,3R,4S,5S,6R)-2-(Acetoxymethyl)-6-(4-nitrophenoxy)tetrahydro-2H-pyran-3,4,5-triacetic acid tris ester
CAS:
13242-51-8
| Molecular Weight: | 469.4 g./mol | Molecular Formula: | C₂₀H₂₃NO₁₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07369606 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is primarily used in biochemical research and enzymatic studies. It serves as a substrate for glycosidases, particularly mannosidases, to investigate enzyme activity and specificity. This compound is valuable in studying carbohydrate metabolism and the mechanisms of glycoside hydrolases. Additionally, it is utilized in the development of assays to measure enzyme kinetics and inhibition, aiding in the discovery of potential therapeutic agents targeting glycosidase-related pathways. Its application extends to the synthesis of complex glycoconjugates, contributing to advancements in glycobiology and the understanding of carbohydrate-protein interactions.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Yellow Solid |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £274.80 |
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4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside
4-Nitrophenyl 2,3,4,6-tetra-O-acetyl-a-D-mannopyranoside is primarily used in biochemical research and enzymatic studies. It serves as a substrate for glycosidases, particularly mannosidases, to investigate enzyme activity and specificity. This compound is valuable in studying carbohydrate metabolism and the mechanisms of glycoside hydrolases. Additionally, it is utilized in the development of assays to measure enzyme kinetics and inhibition, aiding in the discovery of potential therapeutic agents targeting glycosidase-related pathways. Its application extends to the synthesis of complex glycoconjugates, contributing to advancements in glycobiology and the understanding of carbohydrate-protein interactions.
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