2-Methylbutyl (1-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyltetrahydrofuran-2-yl)-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl)carbamate
≥95%
- Product Code: 36112
CAS:
910129-15-6
| Molecular Weight: | 359.35 g./mol | Molecular Formula: | C₁₅H₂₂FN₃O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23135645 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
2-Methylbutyl (1-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyltetrahydrofuran-2-yl)-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl)carbamate is primarily used in the field of medicinal chemistry and pharmaceutical research. It is a derivative of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. The compound's structure, featuring a fluorinated pyrimidine ring, makes it a potential candidate for inhibiting viral replication, particularly in viruses that rely on nucleic acid synthesis, such as HIV or hepatitis viruses. Additionally, its carbamate group enhances its ability to penetrate cell membranes, improving its bioavailability and therapeutic efficacy. Researchers are exploring its application in targeted therapies, where it could be used to selectively disrupt the growth of cancer cells or inhibit viral enzymes without significantly affecting healthy cells. Its unique chemical structure also makes it a valuable tool in studying enzyme mechanisms and drug resistance in pathogens.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿12,861.00 |
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| 0.050 | 10-20 days | ฿21,483.00 |
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2-Methylbutyl (1-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyltetrahydrofuran-2-yl)-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl)carbamate
2-Methylbutyl (1-((2R,3R,4S,5R)-3,4-dihydroxy-5-methyltetrahydrofuran-2-yl)-5-fluoro-2-oxo-1,2-dihydropyrimidin-4-yl)carbamate is primarily used in the field of medicinal chemistry and pharmaceutical research. It is a derivative of nucleoside analogs, which are crucial in the development of antiviral and anticancer drugs. The compound's structure, featuring a fluorinated pyrimidine ring, makes it a potential candidate for inhibiting viral replication, particularly in viruses that rely on nucleic acid synthesis, such as HIV or hepatitis viruses. Additionally, its carbamate group enhances its ability to penetrate cell membranes, improving its bioavailability and therapeutic efficacy. Researchers are exploring its application in targeted therapies, where it could be used to selectively disrupt the growth of cancer cells or inhibit viral enzymes without significantly affecting healthy cells. Its unique chemical structure also makes it a valuable tool in studying enzyme mechanisms and drug resistance in pathogens.
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