Department of Chemistry, Duke University, 124 Science Drive, Durham, NC 27705, USA.
Chem Commun (Camb). 2020 Mar 24;56(24):3555-3558. doi: 10.1039/d0cc00266f.
This study establishes the applicability of imine-based dynamic combinatorial chemistry to discover non-covalent ligands for RNA targets. We elucidate properties underlying the reactivity of arylamines and demonstrate target-guided amplification of tight binders in an amiloride-based dynamic library.
本研究确立了基于亚胺的动态组合化学在发现 RNA 靶标非共价配体方面的适用性。我们阐明了芳胺反应性的基础,并在基于阿米洛利的动态文库中证明了靶标引导的紧密结合物的扩增。