1. PROTAC Autophagy Apoptosis
  2. E3 Ligase Ligand-Linker Conjugates Autophagy Apoptosis
  3. Thalidomide-O-amido-C8-NH2 hydrochloride

Thalidomide-O-amido-C8-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.

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

Thalidomide-O-amido-C8-NH2 hydrochloride Chemical Structure

Thalidomide-O-amido-C8-NH2 hydrochloride Chemical Structure

CAS No. : 2415263-07-7

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Based on 1 publication(s) in Google Scholar

Other Forms of Thalidomide-O-amido-C8-NH2 hydrochloride:

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1 Publications Citing Use of MCE Thalidomide-O-amido-C8-NH2 hydrochloride

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Description

Thalidomide-O-amido-C8-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].

IC50 & Target

Cereblon

 

In Vitro

Thalidomide-O-amido-C8-NH2 is a degron-linker (refer to Compound DL7-TL). The PROTAC linker is bound lo at least one targeting ligand. Degron-linker-targeting ligand, wherein the linker is covalently bound lo at least one degron and at least one targeting ligand, the degron is a compound capable of binding to an ubiquitin ligase such as an E3 ubiquitin ligase (e g, cereblon), and the targeting ligand is capable of binding to the targeted protein(s)[1].

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

Molecular Weight

494.97

Formula

C23H31ClN4O6

CAS No.
SMILES

O=C(NCCCCCCCCN)COC1=CC=CC(C(N2C(CC3)C(NC3=O)=O)=O)=C1C2=O.Cl

Shipping

Room temperature in continental US; may vary elsewhere.

Storage

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

Purity & Documentation
References
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Product Name:
Thalidomide-O-amido-C8-NH2 hydrochloride
Cat. No.:
HY-107439A
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