CNRS, UMR 8638, Synthèse et structure de molécules d'intérêt pharmacologique, 4 avenue de l'Observatoire, 75006 Paris, France.
Biochimie. 2012 Jul;94(7):1607-19. doi: 10.1016/j.biochi.2012.02.002. Epub 2012 Feb 13.
Fragment-based drug design has become increasingly popular over the last decade. We review here the use of this approach to design small RNA binders. In addition, we discuss the use of NMR to detect the binding of small molecules on RNA targets and to guide chemists in the design of compounds targeting RNA.
片段基药物设计在过去十年中变得越来越流行。我们在这里回顾了使用这种方法设计小分子 RNA 结合物的情况。此外,我们还讨论了使用 NMR 来检测小分子与 RNA 靶标的结合,并指导化学家设计针对 RNA 的化合物。