E3 ligase Ligand-Linker Conjugates 55
- Product Code: 106195
CAS:
2328070-52-4
| Molecular Weight: | 476.48 g./mol | Molecular Formula: | C₂₂H₂₈N₄O₈ |
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| Density: | Storage Condition: | -20°C, dry, sealed |
Product Description:
E3 ligase Ligand-Linker Conjugates 55 are primarily utilized in the development of PROTACs (Proteolysis Targeting Chimeras), a cutting-edge technology in targeted protein degradation. These conjugates play a crucial role in bridging the E3 ubiquitin ligase and the target protein of interest, facilitating the ubiquitination and subsequent degradation of the target protein by the proteasome. This approach is particularly valuable in drug discovery and therapeutic research, as it enables the selective elimination of disease-causing proteins, including those traditionally considered "undruggable." By leveraging this mechanism, researchers can explore novel treatments for cancers, neurodegenerative diseases, and other conditions driven by aberrant protein activity. The specific design of Ligand-Linker Conjugate 55 allows for optimized binding and efficiency, making it a key tool in advancing targeted protein degradation strategies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $2,468.11 |
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E3 ligase Ligand-Linker Conjugates 55
E3 ligase Ligand-Linker Conjugates 55 are primarily utilized in the development of PROTACs (Proteolysis Targeting Chimeras), a cutting-edge technology in targeted protein degradation. These conjugates play a crucial role in bridging the E3 ubiquitin ligase and the target protein of interest, facilitating the ubiquitination and subsequent degradation of the target protein by the proteasome. This approach is particularly valuable in drug discovery and therapeutic research, as it enables the selective elimination of disease-causing proteins, including those traditionally considered "undruggable." By leveraging this mechanism, researchers can explore novel treatments for cancers, neurodegenerative diseases, and other conditions driven by aberrant protein activity. The specific design of Ligand-Linker Conjugate 55 allows for optimized binding and efficiency, making it a key tool in advancing targeted protein degradation strategies.
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