1. PROTAC Autophagy Apoptosis
  2. E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis
  3. Thalidomide-O-PEG4-amine

Thalidomide-O-PEG4-amine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.

The free form of the compound is prone to instability, it is advisable to consider the stable salt form (Thalidomide-O-PEG4-amine hydrochloride) that retains the same biological activity.

For research use only. We do not sell to patients.

Thalidomide-O-PEG4-amine Chemical Structure

Thalidomide-O-PEG4-amine Chemical Structure

CAS No. : 2401832-00-4

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Description

Thalidomide-O-PEG4-amine is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology.

IC50 & Target[1]

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].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

493.51

Formula

C23H31N3O9

CAS No.
SMILES

O=C1N(C(CC2)C(NC2=O)=O)C(C3=C1C=CC=C3OCCOCCOCCOCCOCCN)=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
Thalidomide-O-PEG4-amine
Cat. No.:
HY-141010
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