A Chemical Probe for the ATAD2 Bromodomain.

A Chemical Probe for the ATAD2 Bromodomain.
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DOI:
10.1002/anie.201603928
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发表时间:
2016-09-12
期刊:
Angewandte Chemie (International ed. in English)
影响因子:
--
通讯作者:
Watson RJ
Watson RJ
中科院分区:
其他
文献类型:
--
作者:
Bamborough P;Chung CW;Demont EH;Furze RC;Bannister AJ;Che KH;Diallo H;Douault C;Grandi P;Kouzarides T;Michon AM;Mitchell DJ;Prinjha RK;Rau C;Robson S;Sheppard RJ;Upton R;Watson RJ

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ATAD 2是一种癌症相关蛋白,其布罗莫结构域被描述为该目标类别中最难药物化的。从有效的先导化合物开始,通过双重方法提高了渗透性和选择性:1)使用CF 2作为砜生物电子等排体以利用氟的独特性质,以及2)使用1,3-相互作用来控制哌啶环的构象。这导致了首次报道的ATAD 2的低纳摩尔、选择性和细胞可渗透的化学探针。
ATAD2 is a cancer-associated protein whose bromodomain has been described as among the least druggable of that target class. Starting from a potent lead, permeability and selectivity were improved through a dual approach: 1) using CF2 as a sulfone bio-isostere to exploit the unique properties of fluorine, and 2) using 1,3-interactions to control the conformation of a piperidine ring. This resulted in the first reported low-nanomolar, selective and cell permeable chemical probe for ATAD2.
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