| Literature DB >> 28283335 |
Masahiro Ito1, Misa Iwatani2, Yusuke Kamada2, Satoshi Sogabe2, Shoichi Nakao2, Toshio Tanaka2, Tomohiro Kawamoto2, Samuel Aparicio3, Atsushi Nakanishi2, Yasuhiro Imaeda4.
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.Entities:
Keywords: ATP-competitive type inhibitors; Eukaryotic initiation factor 4A3 (eIF4A3) inhibitors; Exon junction complex (EJC); Isothermal titration calorimetry (ITC); RNA helicase; Surface plasmon resonance (SPR)
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Year: 2017 PMID: 28283335 DOI: 10.1016/j.bmc.2017.02.035
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641