(S,R,S)-AHPC-PEG4-N3
≥98%
- Product Code: 99248
CAS:
1797406-81-5
| Molecular Weight: | 689.8200000000001 g./mol | Molecular Formula: | C₃₂H₄₇N₇O₈S |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
(S,R,S)-AHPC-PEG4-N3 is widely utilized in the field of targeted protein degradation and chemical biology. Its primary application lies in the development of PROTACs (Proteolysis Targeting Chimeras), which are bifunctional molecules designed to induce the degradation of specific proteins within cells. The compound’s structure, featuring a PEG4 linker and an azide group, allows for efficient conjugation with other functional moieties, such as E3 ligase ligands or target protein binders. This enables the creation of highly specific and effective degraders for proteins of interest, particularly in cancer research and drug discovery. Additionally, its use in click chemistry reactions, facilitated by the azide group, makes it a valuable tool for labeling and tracking biomolecules in cellular studies. Overall, it plays a critical role in advancing therapeutic strategies and understanding protein function in disease contexts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿35,000.00 |
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| 0.500 | 10-20 days | ฿145,160.00 |
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(S,R,S)-AHPC-PEG4-N3
(S,R,S)-AHPC-PEG4-N3 is widely utilized in the field of targeted protein degradation and chemical biology. Its primary application lies in the development of PROTACs (Proteolysis Targeting Chimeras), which are bifunctional molecules designed to induce the degradation of specific proteins within cells. The compound’s structure, featuring a PEG4 linker and an azide group, allows for efficient conjugation with other functional moieties, such as E3 ligase ligands or target protein binders. This enables the creation of highly specific and effective degraders for proteins of interest, particularly in cancer research and drug discovery. Additionally, its use in click chemistry reactions, facilitated by the azide group, makes it a valuable tool for labeling and tracking biomolecules in cellular studies. Overall, it plays a critical role in advancing therapeutic strategies and understanding protein function in disease contexts.
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