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Updated: Jul 5, 2025

Kinase Inhibitor Screening In Self-assembled Human Protein Microarrays
Published on: October 23, 2019
Discovery of IRAK4 Inhibitors BAY1834845 (Zabedosertib) and BAY1830839
Ulrich Bothe1, Judith Günther1, Reinhard Nubbemeyer1
1Bayer AG, Research & Development, Pharmaceuticals, 13353 Berlin, Germany.
Abstract:
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.

