Identification of RIPK3 Type II Inhibitors Using High-Throughput Mechanistic Studies in Hit Triage

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. Utilizat...

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Veröffentlicht in:ACS medicinal chemistry letters 2020-03, Vol.11 (3), p.266-271
Hauptverfasser: Hart, Amy C, Abell, Lynn, Guo, Junqing, Mertzman, Michael E, Padmanabha, Ramesh, Macor, John E, Chaudhry, Charu, Lu, Hao, O’Malley, Kevin, Shaw, Patrick J, Weigelt, Carolyn, Pokross, Matthew, Kish, Kevin, Kim, Kyoung S, Cornelius, Lyndon, Douglas, Andrew E, Calambur, Deepa, Zhang, Ping, Carpenter, Brian, Pitts, William J
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Sprache:eng
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Zusammenfassung: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.
ISSN:1948-5875
1948-5875
DOI:10.1021/acsmedchemlett.9b00065