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Drug development: Allosteric inhibitors hit USP7 hard
Nature Chemical Biology ( IF 14.8 ) Pub Date : 2018-01-16 , DOI: 10.1038/nchembio.2557
Wei Zhang , Sachdev S Sidhu

Drug development: Allosteric inhibitors hit USP7 hard

Drug development: Allosteric inhibitors hit USP7 hard, Published online: 16 January 2018; doi:10.1038/nchembio.2557

A potent and specific small-molecule inhibitor of a long-sought-after anticancer drug target, USP7, that acts allosterically to inhibit MDM2-stabilizing activity foretells of more allosteric inhibitors for deubiquitinases and E3 ligases.


中文翻译:

药物开发:变构抑制剂对USP7的打击很大

药物开发:变构抑制剂对USP7的打击很大

药物开发:变构抑制剂对USP7造成了沉重打击,在线发布:2018年1月16日; doi:10.1038 / nchembio.2557

一种长期寻求的抗癌药物USP7的有效和特异性小分子抑制剂,具有变构作用,可抑制MTT2的稳定化活性,从而预示着更多的变构抑制剂对泛素化酶和E3连接酶的抑制作用。
更新日期:2018-01-17
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