(2R,3S,4S,5R)-2-(6-Amino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol

≥95%

  • Product Code: 43857
  CAS:    75059-22-2
Molecular Weight: 269.23 g./mol Molecular Formula: C₁₀H₁₂FN₅O₃
EC Number: MDL Number: MFCD20134043
Melting Point: Boiling Point: 628.6°C at 760 mmHg
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. It serves as a modified nucleoside, often incorporated into the development of antiviral and anticancer drugs. Its fluorinated structure enhances its ability to inhibit viral replication by interfering with the synthesis of viral DNA or RNA. This makes it a valuable component in the design of treatments for viral infections, particularly those caused by DNA viruses. Additionally, its potential to disrupt cellular processes in rapidly dividing cells has led to its exploration in cancer therapy, where it may act as a chemotherapeutic agent. Researchers also study its role in understanding enzyme mechanisms and nucleotide metabolism, contributing to advancements in biochemistry and molecular biology.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.010 10-20 days ฿12,618.00
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0.100 10-20 days ฿31,563.00
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(2R,3S,4S,5R)-2-(6-Amino-9H-purin-9-yl)-4-fluoro-5-(hydroxymethyl)tetrahydrofuran-3-ol
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a modified nucleoside, often incorporated into the development of antiviral and anticancer drugs. Its fluorinated structure enhances its ability to inhibit viral replication by interfering with the synthesis of viral DNA or RNA. This makes it a valuable component in the design of treatments for viral infections, particularly those caused by DNA viruses. Additionally, its potential to disrupt cellular processes in rapidly dividing cells has led to its exploration in cancer therapy, where it may act as a chemotherapeutic agent. Researchers also study its role in understanding enzyme mechanisms and nucleotide metabolism, contributing to advancements in biochemistry and molecular biology.
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