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m-PEG16-SH, a PEG-based linker for PROTACs, joins two essential ligands critical for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 100 mg | Inquiry | Backorder | Backorder | |
| 500 mg | Inquiry | Backorder | Backorder |
| Description | m-PEG16-SH, a PEG-based linker for PROTACs, joins two essential ligands critical for forming PROTAC molecules and enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells. |
| In vitro | PROTACs consist of two ligands joined by a linker: one ligand binds to an E3 ubiquitin ligase, while the other targets a specific protein. These compounds harness the intracellular ubiquitin-proteasome system for selective protein degradation [1]. |
| Molecular Weight | 752.95 |
| Formula | C33H68O16S |
| Cas No. | 874820-38-9 |
| Relative Density. | 1.092 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
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