Suppr超能文献

选择性ATP竞争性eIF4A3抑制剂的发现。

Discovery of selective ATP-competitive eIF4A3 inhibitors.

作者信息

Ito Masahiro, Iwatani Misa, Kamada Yusuke, Sogabe Satoshi, Nakao Shoichi, Tanaka Toshio, Kawamoto Tomohiro, Aparicio Samuel, Nakanishi Atsushi, Imaeda Yasuhiro

机构信息

Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, 26-1, Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.

Pharmaceutical Research Division, Takeda Pharmaceutical Company Limited, 26-1, Muraoka-Higashi 2-chome, Fujisawa, Kanagawa 251-8555, Japan.

出版信息

Bioorg Med Chem. 2017 Apr 1;25(7):2200-2209. doi: 10.1016/j.bmc.2017.02.035. Epub 2017 Feb 20.

Abstract

Eukaryotic initiation factor 4A3 (eIF4A3), an ATP-dependent RNA helicase, is a core component of exon junction complex (EJC). EJC has a variety of roles in RNA metabolism such as translation, surveillance, and localization of spliced RNA. It is worthwhile to identify selective eIF4A3 inhibitors with a view to investigating the functions of eIF4A3 and EJC further to clarify the roles of the ATPase and helicase activities in cells. Our chemical optimization of hit compound 2 culminated in the discovery of ATP-competitive eIF4A3 inhibitor 18 with submicromolar ATPase inhibitory activity and excellent selectivity over other helicases. Hence, compound 18 could be a valuable chemical probe to elucidate the detailed functions of eIF4A3 and EJC.

摘要

真核生物起始因子4A3(eIF4A3)是一种依赖ATP的RNA解旋酶,是外显子连接复合体(EJC)的核心成分。EJC在RNA代谢中具有多种作用,如翻译、监测和剪接RNA的定位。为了进一步研究eIF4A3和EJC的功能,以阐明ATP酶和解旋酶活性在细胞中的作用,鉴定选择性eIF4A3抑制剂是很有必要的。我们对命中化合物2进行化学优化,最终发现了ATP竞争性eIF4A3抑制剂18,其具有亚微摩尔ATP酶抑制活性,对其他解旋酶具有优异的选择性。因此,化合物18可能是阐明eIF4A3和EJC详细功能的有价值的化学探针。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验