Thalidomide-O-amido-C8-NH2 TFA
≥98%
- Product Code: 106482
CAS:
1950635-15-0
| Molecular Weight: | 458.51 g./mol | Molecular Formula: | C₂₃H₃₀N₄O₆ |
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| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Thalidomide-O-amido-C8-NH2 TFA is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design and synthesis of targeted therapeutics. Its structure, which incorporates a thalidomide moiety, makes it valuable for applications in proteolysis-targeting chimeras (PROTACs). These molecules are engineered to degrade specific proteins by recruiting E3 ubiquitin ligases, thereby marking the target proteins for destruction by the proteasome. This approach is especially promising in cancer therapy, where it can be used to eliminate oncogenic proteins that are otherwise difficult to target with conventional inhibitors. Additionally, its amido-C8-NH2 linker provides flexibility and stability, enhancing its ability to bind both the target protein and the E3 ligase effectively. The TFA (trifluoroacetic acid) salt form ensures solubility and ease of handling in experimental settings. Researchers also explore its potential in treating inflammatory and autoimmune diseases by modulating protein levels involved in these pathways. Its application extends to chemical biology studies, where it serves as a tool to investigate protein function and degradation mechanisms in cellular systems.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿40,500.00 |
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Thalidomide-O-amido-C8-NH2 TFA
Thalidomide-O-amido-C8-NH2 TFA is primarily utilized in the field of medicinal chemistry and drug development, particularly in the design and synthesis of targeted therapeutics. Its structure, which incorporates a thalidomide moiety, makes it valuable for applications in proteolysis-targeting chimeras (PROTACs). These molecules are engineered to degrade specific proteins by recruiting E3 ubiquitin ligases, thereby marking the target proteins for destruction by the proteasome. This approach is especially promising in cancer therapy, where it can be used to eliminate oncogenic proteins that are otherwise difficult to target with conventional inhibitors. Additionally, its amido-C8-NH2 linker provides flexibility and stability, enhancing its ability to bind both the target protein and the E3 ligase effectively. The TFA (trifluoroacetic acid) salt form ensures solubility and ease of handling in experimental settings. Researchers also explore its potential in treating inflammatory and autoimmune diseases by modulating protein levels involved in these pathways. Its application extends to chemical biology studies, where it serves as a tool to investigate protein function and degradation mechanisms in cellular systems.
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