Thalidomide-Piperazine-PEG3-NH2
Modify Date: 2024-01-06 11:16:07
Thalidomide-Piperazine-PEG3-NH2 structure
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Common Name | Thalidomide-Piperazine-PEG3-NH2 | ||
|---|---|---|---|---|
| CAS Number | 2357113-68-7 | Molecular Weight | 517.57 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C25H35N5O7 | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of Thalidomide-Piperazine-PEG3-NH2Thalidomide-Piperazine-PEG3-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1]. |
| Name | Thalidomide-Piperazine-PEG3-NH2 |
|---|
| Description | Thalidomide-Piperazine-PEG3-NH2 is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[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[2]. |
| References |
| Molecular Formula | C25H35N5O7 |
|---|---|
| Molecular Weight | 517.57 |