Max Planck Institute for Molecular Physiology, Department of Chemical Biology, Otto-Hahn-Strasse 11, Dortmund 44227, Germany; Technische Universität Dortmund, Faculty of Chemistry and Chemical Biology, Otto-Hahn-Strasse 6, Dortmund 44227, Germany.
Max Planck Institute for Molecular Physiology, Department of Chemical Biology, Otto-Hahn-Strasse 11, Dortmund 44227, Germany.
Cell Chem Biol. 2019 Apr 18;26(4):512-523.e5. doi: 10.1016/j.chembiol.2018.11.014. Epub 2019 Jan 24.
Small-molecule chemotypes with unexpected bioactivity may be identified by combining strategies built on the biological relevance of, e.g., natural products (NPs), such as biology-oriented synthesis, with principles that enable efficient coverage of chemical space, such as fragment-based compound design. Evaluation in target-agnostic phenotypic assays and target identification may link biologically relevant chemotypes to unexpected and unknown targets. We describe the phenotypic identification of an unprecedented kinase inhibitor chemotype obtained by synthetic combination of two biosynthetically unrelated NP fragment types. Target identification and biological characterization revealed that the inhibitor, termed Myokinasib, impairs cytokinesis, induces formation of multinucleated cells, and reduces phosphorylated myosin II light chain abundance on stress fibers by selective inhibition of myosin light chain kinase 1.
小分子化学型具有意想不到的生物活性,可通过将基于天然产物(NPs)的生物学相关性的策略(例如,面向生物学的合成)与能够有效覆盖化学空间的原则(例如,基于片段的化合物设计)相结合来识别。在无靶点表型测定和靶点鉴定中的评估可以将具有生物学相关性的化学型与意想不到的未知靶点联系起来。我们描述了一种通过两种生物合成上无关的 NP 片段类型的合成组合获得的前所未有的激酶抑制剂化学型的表型鉴定。靶点鉴定和生物学特征表明,该抑制剂(称为 Myokinasib)通过选择性抑制肌球蛋白轻链激酶 1,损害胞质分裂,诱导多核细胞形成,并减少应激纤维上磷酸化肌球蛋白 II 轻链的丰度。