(S,R,S)-AHPC-C6-PEG3-C4-Cl 由 E3 配体与 20 个原子相连的复合分子，连接子的接头为 Halogen 基团。(S,R,S)-AHPC-C6-PEG3-C4-Cl 包含基于 (S,R,S)-AHPC 的 VHL 配体和 基于一个 alkyl/ether linker。(S,R,S)-AHPC-C6-PEG3-C4-Cl 能够诱导 GFP-HaloTag7 降解。

(S,R,S)-AHPC-C6-PEG3-C4-Cl (VH032-C6-PEG3-C4-Cl) is a conjugate of ligands for E3 and 20-atom-length linker. The connector of linker is Halogen group. (S,R,S)-AHPC-C6-PEG3-C4-Cl incorporates the (S,R,S)-AHPC based VHL ligand and an alkyl/ether-based linker. (S,R,S)-AHPC-C6-PEG3-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays.

Oil

VHL

(S,R,S)-AHPC-C6-PEG3-C4-Cl uses the cereblon ligand. The linker is 6-2-2-6. The linkers contain a mixture of hydrophobic and hydrophilic moieties to balance the hydrophobicity/hydrophilicity of the resulting hybrid compounds. PROTACs that induce the degradation of an oncogenic tyrosine kinase, BCR-ABL has been developed. (S,R,S)-AHPC-C6-PEG3-C4-Cl can be attached to potent TKIs (bosutinib and dasatinib) that mediate the degradation of c-ABL and BCR-ABL by hijacking either CRBN or VHL E3 ubiquitin ligase . has not independently confirmed the accuracy of these methods. They are for reference only.

Room temperature in continental US; may vary elsewhere.

Pure form -20°C 3 years；4°C 2 years

[1]. Lai AC, et al. Modular PROTAC Design for the Degradation of Oncogenic BCR-ABL. Angew Chem Int Ed Engl. 2016 Jan 11;55(2):807-10.
[2]. US 20170121321 A1

In Vitro: Ethanol : 100 mg/mL (133.08 mM; Need ultrasonic)DMSO : ≥ 100 mg/mL (133.08 mM)