Sodium ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate hydrate(2:1:x)
≥95%
- Product Code: 47954
CAS:
146877-92-1
| Molecular Weight: | 409.20 g./mol | Molecular Formula: | C₁₀H₁₄N₅Na₂O₈P |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in biochemical research and pharmaceutical development due to its role as a nucleotide analog. It is often employed in studies related to DNA and RNA synthesis, where it acts as a precursor or building block in enzymatic reactions. Its structure allows it to mimic natural nucleotides, making it valuable for investigating metabolic pathways, enzyme mechanisms, and nucleic acid interactions. Additionally, it is used in the development of antiviral and anticancer drugs, where it can interfere with the replication of genetic material in targeted cells. Its hydrate form ensures stability and solubility, making it suitable for experimental and therapeutic applications.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White Solid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | £6.79 |
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| 10.000 | 10-20 days | £10.18 |
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| 25.000 | 10-20 days | £20.58 |
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Sodium ((2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl phosphate hydrate(2:1:x)
This compound is primarily utilized in biochemical research and pharmaceutical development due to its role as a nucleotide analog. It is often employed in studies related to DNA and RNA synthesis, where it acts as a precursor or building block in enzymatic reactions. Its structure allows it to mimic natural nucleotides, making it valuable for investigating metabolic pathways, enzyme mechanisms, and nucleic acid interactions. Additionally, it is used in the development of antiviral and anticancer drugs, where it can interfere with the replication of genetic material in targeted cells. Its hydrate form ensures stability and solubility, making it suitable for experimental and therapeutic applications.
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