作者:Marc J. Adler、Andrew D. Hamilton
DOI:10.1021/jo200917d
日期:2011.9.2
The design and synthesis of small molecule α-helix mimetics has been a productive field over the past decade. These compounds have performed well in a variety of biological systems as functional disruptors of α-helix-mediated protein–protein interactions. In our studies we have continued to develop novel, more biologically compatible scaffolds, which are often easier to assemble and capable of mimicking
在过去的十年中,小分子α-螺旋模拟物的设计和合成一直是一个生产领域。这些化合物作为α-螺旋介导的蛋白质-蛋白质相互作用的功能破坏者,在各种生物系统中均表现良好。在我们的研究中,我们一直在开发新型的,生物相容性更高的支架,这些支架通常更易于组装并且能够模仿更长和/或更多样化的螺旋。为此,我们基于烯胺酮支架构建了一系列新的i,i + 4,i + 7α-螺旋模拟物。这些分子代表了在追求理想化的单面α-螺旋模拟物方面的进步。