6-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-7H-purine-8(9H)-thione
97%
- Product Code: 71165
CAS:
3001-45-4
| Molecular Weight: | 299.31 g./mol | Molecular Formula: | C₁₀H₁₃N₅O₄S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 640.3°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in biochemical research and pharmaceutical development due to its structural similarity to nucleosides, which are essential components of DNA and RNA. It serves as a key intermediate in the synthesis of modified nucleosides or nucleotides, which are often explored for their potential antiviral, anticancer, or antimicrobial properties. Researchers use it to study enzyme interactions, particularly those involving nucleoside-metabolizing enzymes, to develop targeted therapies. Additionally, it may be employed in the design of prodrugs or as a building block in the creation of novel therapeutic agents aimed at modulating cellular processes. Its thione group also makes it a candidate for investigating sulfur-containing nucleoside analogs, which can have unique biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿720.00 |
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| 0.250 | 10-20 days | ฿1,440.00 |
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6-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-7H-purine-8(9H)-thione
This compound is primarily utilized in biochemical research and pharmaceutical development due to its structural similarity to nucleosides, which are essential components of DNA and RNA. It serves as a key intermediate in the synthesis of modified nucleosides or nucleotides, which are often explored for their potential antiviral, anticancer, or antimicrobial properties. Researchers use it to study enzyme interactions, particularly those involving nucleoside-metabolizing enzymes, to develop targeted therapies. Additionally, it may be employed in the design of prodrugs or as a building block in the creation of novel therapeutic agents aimed at modulating cellular processes. Its thione group also makes it a candidate for investigating sulfur-containing nucleoside analogs, which can have unique biological activities.
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