| Literature DB >> 30686759 |
Tabea Schneidewind1, Shobhna Kapoor2, Guillaume Garivet2, George Karageorgis2, Rishikesh Narayan2, Gloria Vendrell-Navarro2, Andrey P Antonchick2, Slava Ziegler2, Herbert Waldmann3.
Abstract
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.Keywords: biology-oriented synthesis; chemical biology; cytokinesis; cytokinesis failure; kinase inhibitor; myosin light chain kinase; natural products; pseudo natural products; small molecules
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Year: 2019 PMID: 30686759 DOI: 10.1016/j.chembiol.2018.11.014
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116