| Literature DB >> 32184965 |
Naomi S Rajapaksa1, Alberto Gobbi1, Joy Drobnick1, Steven Do1, Aleksandr Kolesnikov1, Jun Liang1, Yongsheng Chen2, Swathi Sujatha-Bhaskar1, Zhiyu Huang1, Hans Brightbill1, Ross Francis1, Christine Yu1, Edna F Choo1, Kevin DeMent1, Yingqing Ran1, Le An1, Claire Emson1, Jonathan Maher1, John Wai2, Brent S McKenzie1, Patrick J Lupardus1, Ali A Zarrin1, James R Kiefer1, Marian C Bryan1.
Abstract
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.Entities:
Year: 2019 PMID: 32184965 PMCID: PMC7073891 DOI: 10.1021/acsmedchemlett.9b00380
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345