((2S,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-azido-4-fluorotetrahydrofuran-2-yl)methanol
95%
- Product Code: 84751
CAS:
123334-79-2
| Molecular Weight: | 294.25 g./mol | Molecular Formula: | C₁₀H₁₁FN₈O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the development of nucleoside analogs, which are crucial in antiviral and anticancer research. Its structure, featuring an azido group and a fluorine atom, allows it to act as a key intermediate in the synthesis of modified nucleosides. These modifications are essential for enhancing the binding affinity and selectivity of nucleoside-based drugs to their target enzymes or receptors. Additionally, the azido group provides a handle for further chemical modifications, enabling the attachment of various functional groups or probes for biochemical studies. This compound is particularly valuable in the study of RNA and DNA metabolism, as well as in the design of novel therapeutic agents that can inhibit viral replication or interfere with cancer cell proliferation. Its unique structural features make it a versatile tool in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿18,720.00 |
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| 0.250 | 10-20 days | ฿35,100.00 |
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((2S,3R,4R,5R)-5-(6-amino-9H-purin-9-yl)-3-azido-4-fluorotetrahydrofuran-2-yl)methanol
This chemical is primarily utilized in the development of nucleoside analogs, which are crucial in antiviral and anticancer research. Its structure, featuring an azido group and a fluorine atom, allows it to act as a key intermediate in the synthesis of modified nucleosides. These modifications are essential for enhancing the binding affinity and selectivity of nucleoside-based drugs to their target enzymes or receptors. Additionally, the azido group provides a handle for further chemical modifications, enabling the attachment of various functional groups or probes for biochemical studies. This compound is particularly valuable in the study of RNA and DNA metabolism, as well as in the design of novel therapeutic agents that can inhibit viral replication or interfere with cancer cell proliferation. Its unique structural features make it a versatile tool in medicinal chemistry and drug discovery.
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