| Name | Thalidomide-O-amido-PEG-C2-NH2 hydrochloride |
|---|---|
| Synonyms | MFCD32063469 |
| Description | Thalidomide-O-amido-PEG-C2-NH2 hydrochloride, a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker, can be used in the synthesis of PROTACs[1]. |
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| Related Catalog | |
| Target |
Cereblon |
| 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 | C19H23ClN4O7 |
|---|---|
| Molecular Weight | 454.86 |
| Hazard Codes | Xi |
|---|