AE18677
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $75.00 | $52.00 | - + | |
250mg | 98% | in stock | $139.00 | $97.00 | - + | |
1g | 98% | in stock | $372.00 | $260.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE18677 |
Chemical Name: | 9-(2-Deoxy-2-fluoroarabinofuranosyl)guanine |
CAS Number: | 103884-98-6 |
Molecular Formula: | C10H12FN5O4 |
Molecular Weight: | 285.2318 |
MDL Number: | MFCD01694134 |
SMILES: | OC[C@H]1OC([C@H]([C@@H]1O)F)n1cnc2c1nc(N)[nH]c2=O |
9-(2-Deoxy-2-fluoroarabinofuranosyl)guanine, commonly referred to as $name$, is a crucial compound in chemical synthesis due to its unique properties and versatile applications. As a fluorinated nucleoside analog, $name$ is widely used in the field of medicinal chemistry for the development of pharmaceuticals targeting viral infections and cancer.One of the key applications of $name$ in chemical synthesis is its role as a potent antiviral agent. Through its ability to mimic nucleosides present in viral DNA/RNA, $name$ exerts its antiviral activity by inhibiting viral replication and disrupting the viral life cycle. This makes it a valuable tool in the development of antiviral drugs targeting viruses such as herpes simplex virus and varicella-zoster virus.Furthermore, the unique fluorinated sugar moiety in $name$ enhances its stability and bioavailability, making it an attractive candidate for prodrug development. By modifying the structure of $name$ through chemical derivatization, researchers can design prodrugs with improved pharmacokinetic properties, such as increased cell permeability and bioactivity.In summary, the application of 9-(2-deoxy-2-fluoroarabinofuranosyl)guanine in chemical synthesis extends beyond its role as a nucleoside analog. Its versatility and potential for structural modification make it a valuable asset in the development of novel antiviral agents and therapeutic interventions in medicinal chemistry.