| Literature DB >> 32184955 |
Amy C Hart1, Lynn Abell1, Junqing Guo1, Michael E Mertzman1, Ramesh Padmanabha1, John E Macor1, Charu Chaudhry1, Hao Lu1, Kevin O'Malley1, Patrick J Shaw1, Carolyn Weigelt1, Matthew Pokross1, Kevin Kish1, Kyoung S Kim1, Lyndon Cornelius1, Andrew E Douglas1, Deepa Calambur1, Ping Zhang1, Brian Carpenter1, William J Pitts1.
Abstract
Necroptosis has been implicated in a variety of disease states, and RIPK3 is one of the kinases identified to play a critical role in this signaling pathway. In an effort to identify RIPK3 kinase inhibitors with a novel profile, mechanistic studies were incorporated at the hit triage stage. Utilization of these assays enabled identification of a Type II DFG-out inhibitor for RIPK3, which was confirmed by protein crystallography. Structure-based drug design on the inhibitors targeting this previously unreported conformation enabled an enhancement in selectivity against key off-target kinases.Entities:
Year: 2019 PMID: 32184955 PMCID: PMC7073880 DOI: 10.1021/acsmedchemlett.9b00065
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345