(S,R,S)-AHPC-PEG2-NH2(Synonyms: VH032-PEG2-NH2 ; VHL Ligand-Linker Conjugates 3 ; E3 ligase Ligand-Linker Conjugates 6 Free Base)

上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。

(S,R,S)-AHPC-PEG2-NH2 (Synonyms: VH032-PEG2-NH2 ; VHL Ligand-Linker Conjugates 3 ; E3 ligase Ligand-Linker Conjugates 6 Free Base)

(S,R,S)-AHPC-PEG2-NH2 (VH032-PEG2-NH2) 是一种合成的 E3 连接酶配体-linker 偶联物,包含基于 (S,R,S)-AHPC 的 VHL 配体和 2 个单元 PEG linker。可用于合成 PROTAC 分子。

(S,R,S)-AHPC-PEG2-NH2(Synonyms: VH032-PEG2-NH2 ;  VHL Ligand-Linker Conjugates 3 ;  E3 ligase Ligand-Linker Conjugates 6 Free Base)

(S,R,S)-AHPC-PEG2-NH2 Chemical Structure

CAS No. : 2010159-60-9

规格 价格 是否有货 数量
100 mg ¥3200 In-stock
500 mg ¥12000 询价
1 g ¥22000 询价
2 g ¥32000 询价
5 g   询价  
10 g   询价  

* Please select Quantity before adding items.

生物活性

(S,R,S)-AHPC-PEG2-NH2 (VH032-PEG2-NH2) is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker used in the synthesis of PROTACs[1].

IC50 & Target[1]

VHL

 

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[1].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

575.72

Formula

C28H41N5O6S

CAS 号

2010159-60-9

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
参考文献
  • [1]. Chan KH, et al. Impact of Target Warhead and Linkage Vector on Inducing Protein Degradation: Comparison of Bromodomain and Extra-Terminal (BET) Degraders Derived from Triazolodiazepine (JQ1) and Tetrahydroquinoline (I-BET726) BET Inhibitor Scaffolds. J Med Chem. 2018 Jan 25;61(2):504-513.

所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务