(2R,3R,4S,5R)-2-(6-(((E)-4-Hydroxy-3-methylbut-2-en-1-yl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
≥95%
- Product Code: 53865
CAS:
28542-78-1
Molecular Weight: | 351.36 g./mol | Molecular Formula: | C₁₅H₂₁N₅O₅ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 731.8°C at 760 mmHg | |
Density: | Storage Condition: | -20°C, dry in the dark |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and biochemistry for its role as a modified nucleoside. It serves as a key intermediate in the synthesis of nucleotide analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to mimic natural nucleosides, enabling it to interfere with viral replication or cancer cell proliferation. Researchers also explore its potential in studying enzyme mechanisms and designing inhibitors for specific biochemical pathways. Additionally, it finds application in the development of prodrugs, where its modifications enhance bioavailability and target specificity.
Product Specification:
Test | Specification |
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APPEARANCE | Solid |
PURITY | 95-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿2,860.00 |
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0.250 | 10-20 days | ฿6,360.00 |
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1.000 | 10-20 days | ฿23,880.00 |
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(2R,3R,4S,5R)-2-(6-(((E)-4-Hydroxy-3-methylbut-2-en-1-yl)amino)-9H-purin-9-yl)-5-(hydroxymethyl)tetrahydrofuran-3,4-diol
This chemical is primarily utilized in the field of medicinal chemistry and biochemistry for its role as a modified nucleoside. It serves as a key intermediate in the synthesis of nucleotide analogs, which are crucial in the development of antiviral and anticancer drugs. Its structure allows it to mimic natural nucleosides, enabling it to interfere with viral replication or cancer cell proliferation. Researchers also explore its potential in studying enzyme mechanisms and designing inhibitors for specific biochemical pathways. Additionally, it finds application in the development of prodrugs, where its modifications enhance bioavailability and target specificity.
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