Discovery of IRAK4 Inhibitors BAY1834845 (Zabedosertib) and BAY1830839

Ulrich Bothe, Judith Guenther,Reinhard Nubbemeyer,Holger Siebeneicher,Sven Ring,Ulf Boemer, Michaele Peters,Alexandra Rausch,Karsten Denner,Herbert Himmel, Andreas Sutter,Ildiko Terebesi,Martin Lange,Antje M. Wengner, Nicolas Guimond, Tobias Thaler, Johannes Platzek, Uwe Eberspaecher,Martina Schaefer,Holger Steuber,Thomas M. Zollner,Andreas Steinmeyer, Nicole Schmidt

JOURNAL OF MEDICINAL CHEMISTRY(2024)

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摘要
Interleukin-1 receptor-associated kinase 4 (IRAK4) plays a critical role in innate inflammatory processes. Here, we describe the discovery of two clinical candidate IRAK4 inhibitors, BAY1834845 (zabedosertib) and BAY1830839, starting from a high-throughput screening hit derived from Bayer's compound library. By exploiting binding site features distinct to IRAK4 using an in-house docking model, liabilities of the original hit could surprisingly be overcome to confer both candidates with a unique combination of good potency and selectivity. Favorable DMPK profiles and activity in animal inflammation models led to the selection of these two compounds for clinical development in patients.
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