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
Bristol-Myers Squibb Research & Development, P.O. Box 4000, Princeton, New Jersey 08543, United States.
ACS Med Chem Lett. 2019 May 6;11(3):266-271. doi: 10.1021/acsmedchemlett.9b00065. eCollection 2020 Mar 12.
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.
坏死性凋亡与多种疾病状态有关,而RIPK3是在该信号通路中发挥关键作用的激酶之一。为了鉴定具有新特性的RIPK3激酶抑制剂,在命中物筛选阶段纳入了机制研究。利用这些测定方法鉴定出一种RIPK3的II型DFG-out抑制剂,该抑制剂通过蛋白质晶体学得到证实。针对这种以前未报道的构象的抑制剂进行基于结构的药物设计,提高了对关键脱靶激酶的选择性。