Identification of highly efficacious PROTACs targeting BRD4 against acute myeloid leukemia:Design,synthesis,and biological evaluations  

在线阅读下载全文

作  者:Aiping Chen Yue Zhong Yunxiao Liu Zhancheng Xie Hanyu Wu Wei Shi Wenlong Huang Renxiang Tan Hai Qian 

机构地区:[1]College of Pharmacy,Nanjing University of Chinese Medicine,Nanjing 210023,China [2]Center of Drug Discovery,State Key Laboratory of Natural Medicines,China Pharmaceutical University,Nanjing 210009,China [3]Jiangsu Key Laboratory of Drug Discovery for Metabolic Disease,China Pharmaceutical University,Nanjing 210009,China

出  处:《Chinese Chemical Letters》2023年第6期426-431,共6页中国化学快报(英文版)

基  金:the National Science Foundation of China(Nos.81872733,82173674,and 81872734);the Research&Development Project in Key Areas of Guangdong Province(No.2019B020203003)for supporting this study。

摘  要:The abnormal activation of BRD4 accelerates the progression of acute myeloid leukemia(AML),developing more precise therapeutics to intervene BRD4 promise to be an excellent opportunity to avoid current limitations of chemotherapy in clinic.Herein,a range of small-molecule PROTACs with the privileged 8-methyl-pyrrolo[1,2-a]pyrazin-1(2H)-one scaffold were rationally designed,which harbored different carbon or ethylenedioxy chains to degrade BRD4 mediated by the E3 ubiquitin ligase CRBN.Among them,the most potential B24 exhibited remarkable BRD4 degradation and excellent anti-proliferative activities in MV4-11 cells,with values of DC_(50)and IC_(50)for 0.75 nmol/L and 0.4 nmol/L,respectively,which were better than the BRD4 inhibitor(+)-JQ-1.Notably,this compound could time-dependently degrade the target protein in the BRD4-,CRBN-,and proteasome-dependent manner.Besides,B24 dramatically decreased the level of proto-oncogene c-Myc,and induced cell apoptosis by arresting the cell cycle in G0/G1 phase,down-regulating Bcl-2 and up-regulating Bax to amplify apoptotic effectors.This proof-of-concept study also highlighted the feasibility of BRD4-based PROTACs as a more powerful strategy against AML.

关 键 词:Acute myeloid leukemia BRD4 PROTACs Protein degradation APOPTOSIS 

分 类 号:R914[医药卫生—药物化学]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象