Discovery of Benzo[
<i>d</i>
]imidazole‐6‐sulfonamides as Bromodomain and Extra‐Terminal Domain (BET) Inhibitors with Selectivity for the First Bromodomain
作者:Alessandra Cipriano、Ciro Milite、Alessandra Feoli、Monica Viviano、Giacomo Pepe、Pietro Campiglia、Giuliana Sarno、Sarah Picaud、Satomi Imaide、Nikolai Makukhin、Panagis Filippakopoulos、Alessio Ciulli、Sabrina Castellano、Gianluca Sbardella
DOI:10.1002/cmdc.202200343
日期:2022.10.19
Bioisosteric replacement of the azobenzene moiety of selective BET inhibitors with a benzimidazole ring afforded a set of benzimidazole-6-sulfonamides. Evaluation of the binding activity against diverse BRD families endorses the benzimidazole as a useful scaffold to obtain compounds with improved selectivity towards the first bromodomains of BET family proteins.
用苯并咪唑环生物等排取代选择性 BET 抑制剂的偶氮苯部分,得到一组苯并咪唑-6-磺酰胺。对不同 BRD 家族的结合活性的评估支持苯并咪唑作为一种有用的支架,以获得对 BET 家族蛋白的第一个溴结构域具有更高选择性的化合物。