Thalidomide 4′-ether-alkylC2-amine hydrochloride

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Thalidomide 4′-ether-alkylC2-amine hydrochloride 

Thalidomide 4′-ether-alkylC2-amine hydrochloride 是一种合成的 E3 连接酶配体-linker 偶联物，包含基于 Thalidomide 的 cereblon 配体和 linker，应用于 PROTAC 技术。

Thalidomide 4

Thalidomide 4′-ether-alkylC2-amine hydrochloride Chemical Structure

CAS No. : 2341840-99-9

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生物活性

Thalidomide 4′-ether-alkylC2-amine hydrochloride is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1].

IC50 & Target

Cereblon

 

体外研究
(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.

Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
分子量

353.76

Formula

C15H16ClN3O5
CAS 号

2341840-99-9
运输条件

Room temperature in continental US; may vary elsewhere.
储存方式

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

  • [1]. Turk BE, et al. Binding of thalidomide to alpha1-acid glycoprotein may be involved in its inhibition of tumor necrosis factor alpha production. Proc Natl Acad Sci U S A. 1996;93(15):7552‐7556.

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