(2R,3S,4R,5R)-2-(Hydroxymethyl)-5-(6-((2-(methylthio)ethyl)amino)-2-((3,3,3-trifluoropropyl)thio)-9H-purin-9-yl)tetrahydrofuran-3,4-diol
97%
- Product Code: 55380
CAS:
163706-58-9
Molecular Weight: | 469.50 g./mol | Molecular Formula: | C₁₆H₂₂F₃N₅O₄S₂ |
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EC Number: | MDL Number: | MFCD15832982 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural complexity and potential biological activity. Its unique structure, featuring purine and tetrahydrofuran moieties, makes it a candidate for the development of nucleoside analogs. These analogs are often explored for their antiviral or anticancer properties, as they can interfere with DNA or RNA synthesis in target cells. The presence of thioether and trifluoropropyl groups enhances its potential to interact with specific enzymes or receptors, making it a valuable scaffold for drug discovery. Researchers may also investigate its pharmacokinetic properties, such as stability, absorption, and metabolism, to optimize its therapeutic efficacy. Additionally, it could serve as a reference compound in biochemical studies to understand cellular processes involving purine metabolism.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $45.20 |
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1.000 | 10-20 days | $103.06 |
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5.000 | 10-20 days | $360.27 |
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(2R,3S,4R,5R)-2-(Hydroxymethyl)-5-(6-((2-(methylthio)ethyl)amino)-2-((3,3,3-trifluoropropyl)thio)-9H-purin-9-yl)tetrahydrofuran-3,4-diol
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural complexity and potential biological activity. Its unique structure, featuring purine and tetrahydrofuran moieties, makes it a candidate for the development of nucleoside analogs. These analogs are often explored for their antiviral or anticancer properties, as they can interfere with DNA or RNA synthesis in target cells. The presence of thioether and trifluoropropyl groups enhances its potential to interact with specific enzymes or receptors, making it a valuable scaffold for drug discovery. Researchers may also investigate its pharmacokinetic properties, such as stability, absorption, and metabolism, to optimize its therapeutic efficacy. Additionally, it could serve as a reference compound in biochemical studies to understand cellular processes involving purine metabolism.
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