(2R,3R,4S,5R)-2-(4-aminopyrrolo[1,2-f][1,2,4]triazin-7-yl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-carbonitrile(GS-441524)
≥98%
- Product Code: 80482
CAS:
1191237-69-0
| Molecular Weight: | 291.26 g./mol | Molecular Formula: | C₁₂H₁₃N₅O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32666994 | |
| Melting Point: | Boiling Point: | ||
| Density: | 1.84±0.1 g/cm3 | Storage Condition: | 2-8°C, dark, dry |
Product Description:
This compound is primarily recognized for its antiviral properties, particularly in the treatment of RNA virus infections. It has shown significant efficacy in inhibiting viral replication, making it a promising candidate for addressing diseases caused by viruses such as coronaviruses. Research has highlighted its potential in reducing viral load and improving clinical outcomes in animal models, suggesting its applicability in combating emerging viral threats. Additionally, its mechanism of action, which involves interfering with viral RNA synthesis, positions it as a valuable tool in the development of antiviral therapies. Studies continue to explore its broader applications in treating other RNA virus infections, underscoring its versatility in antiviral research and drug development.
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 |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,990.00 |
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| 0.250 | 10-20 days | ฿7,390.00 |
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| 1.000 | 10-20 days | ฿14,790.00 |
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(2R,3R,4S,5R)-2-(4-aminopyrrolo[1,2-f][1,2,4]triazin-7-yl)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-carbonitrile(GS-441524)
This compound is primarily recognized for its antiviral properties, particularly in the treatment of RNA virus infections. It has shown significant efficacy in inhibiting viral replication, making it a promising candidate for addressing diseases caused by viruses such as coronaviruses. Research has highlighted its potential in reducing viral load and improving clinical outcomes in animal models, suggesting its applicability in combating emerging viral threats. Additionally, its mechanism of action, which involves interfering with viral RNA synthesis, positions it as a valuable tool in the development of antiviral therapies. Studies continue to explore its broader applications in treating other RNA virus infections, underscoring its versatility in antiviral research and drug development.
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