ACS Medicinal Chemistry Letters · 2019 · 23 citations · 8 references
MedicineMedicinal ChemistryPharmacologyDrug DiscoveryInflammationPharmacodynamicsAnti-inflammatory PharmacologyInflammation PharmacologyInflammatory Disease PharmacotherapyInflammatory SignalingAnti-inflammatory Drug DiscoveryAnti-inflammatory TherapeuticsHuman Disease ModelsIn Vivo StudiesKinase Inhibitor Library DesignKinase Signaling Inhibitors
IRAK4 kinase activity transduces signaling from multiple IL-1Rs and TLRs to regulate cytokines and chemokines implicated in inflammatory diseases. As such, there is high interest in identifying selective IRAK4 inhibitors for the treatment of these disorders. We previously reported the discovery of potent and selective dihydrobenzofuran inhibitors of IRAK4. Subsequent studies, however, showed inconsistent inhibition in disease-relevant pharmacodynamic models. Herein, we describe application of a human whole blood assay to the discovery of a series of benzolactam IRAK4 inhibitors. We identified potent molecule 19 that achieves robust in vivo inhibition of cytokines relevant to human disease.
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Helical assembly in the MyD88–IRAK4–IRAK2 complex in TLR/IL-1R signalling
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Dominic De Nardo, Katherine R. Balka, Yamel Cardona Gloria et al. · Journal of Biological Chemistry · 2018 · 146 citations · Full text
Katherine L. Lee, Catherine M. Ambler, David R. Anderson et al. · Journal of Medicinal Chemistry · 2017 · 145 citations · Full text