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Pomalidomide-amido-C1-Br
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
Pomalidomide-amido-C1-Br图片
CAS NO:2351106-38-0
包装与价格:
包装价格(元)
5mg电议
50mg电议
100mg电议
200mg电议
500mg电议

产品介绍
Pomalidomide-amido-C1-Br 是一种合成的 E3 连接酶配体-linker 偶联物,包含基于 Pomalidomide 的 cereblon 配体和 1 个 linker。Pomalidomide-amido-C1-Br 可通过 PROTAC 技术合成 B-Raf 降解剂 PROTAC B-Raf degrader 1 (HY-111758)。PROTAC B-Raf degrader 1 具有抗肿瘤活性。
生物活性

Pomalidomide-amido-C1-Br is a synthesizedE3 ligase ligand-linker conjugatethat incorporates the Pomalidomide basedcereblonligand and a linker. Pomalidomide-amido-C1-Br can be used to design a B-RafPROTACdegraderPROTACB-Raf degrader 1 (HY-111758).PROTACB-Raf degrader 1 has anti-cancer activity[1].

IC50& Target[1]

Cereblon

 

体外研究
(In Vitro)

Pomalidomide-amido-C1-Br (Compound 6) can be used to design a B-Raf PROTAC degrader PROTAC B-Raf degrader 1 (Compound 2). PROTAC B-Raf degrader 1 can effectively kill cancer cells via inducing cells apoptosis. As a B-Raf degrader, PROTAC B-Raf degrader 1 can accelerate the degradation of B-Raf by recruiting ubiquitin-proteasome system, and further affects the expression of Mcl-1, a downstream protein of B-Raf[1].

分子量

394.18

性状

Solid

Formula

C15H12BrN3O5

CAS 号

2351106-38-0

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

4°C, stored under nitrogen

*In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen)