N2-Isobutyryl-2'-fluoro-2'-deoxyguanosine

98%

  • Product Code: 97311
  CAS:    80681-25-0
Molecular Weight: 355.32 g./mol Molecular Formula: C₁₄H₁₈FN₅O₅
EC Number: MDL Number: MFCD15145246
Melting Point: Boiling Point:
Density: 1.78±0.1 g/cm3(Predicted) Storage Condition: 2-8°C, dry, sealed
Product Description: N2-Isobutyryl-2'-fluoro-2'-deoxyguanosine is primarily utilized in the field of nucleoside chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of modified nucleosides, which are essential for developing antiviral and anticancer drugs. The presence of the fluorine atom at the 2' position enhances the stability and binding affinity of the nucleoside to target enzymes, making it valuable for designing therapeutic agents. This compound is particularly significant in the study of RNA and DNA analogs, where it helps in understanding the mechanisms of viral replication and cellular processes. Additionally, it is employed in the development of prodrugs, improving the bioavailability and efficacy of nucleoside-based treatments. Its application extends to molecular biology, where it aids in the study of nucleic acid interactions and the design of novel therapeutic strategies.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿4,491.00
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0.250 10-20 days ฿6,291.00
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1.000 10-20 days ฿15,273.00
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N2-Isobutyryl-2'-fluoro-2'-deoxyguanosine
N2-Isobutyryl-2'-fluoro-2'-deoxyguanosine is primarily utilized in the field of nucleoside chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of modified nucleosides, which are essential for developing antiviral and anticancer drugs. The presence of the fluorine atom at the 2' position enhances the stability and binding affinity of the nucleoside to target enzymes, making it valuable for designing therapeutic agents. This compound is particularly significant in the study of RNA and DNA analogs, where it helps in understanding the mechanisms of viral replication and cellular processes. Additionally, it is employed in the development of prodrugs, improving the bioavailability and efficacy of nucleoside-based treatments. Its application extends to molecular biology, where it aids in the study of nucleic acid interactions and the design of novel therapeutic strategies.
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