| Name | Thalidomide-O-amido-PEG4-azide |
|---|---|
| Synonyms | MFCD32670309 |
| Description | Thalidomide-O-amido-PEG4-azide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. |
|---|---|
| Related Catalog | |
| Target |
PEGs |
| In Vitro | PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1]. |
| References |
| Molecular Formula | C25H32N6O10 |
|---|---|
| Molecular Weight | 576.56 |