作者
Angela Mackay,Juraj Velcicky,Nina Gommermann,Henri Mattes,Philipp Janser,Michael Wright,Celine Dubois,Silke Brenneisen,Slavica Ilić,Eric Vangrevelinghe,Nikolaus Stiefl,Andreas Boettcher,Michel Schoenboerner,Melanie Vogelsanger,Sophie Muller-Bentz,Marion Kamke,Joëlle Rubert,Muriel Kauffmann,Sandrine Desrayaud,Markus Trunzer,Srinivas Honnappa,Alexandra Hinniger,Nicole von Burg,Karen Beltz,Carien Dekker,Christopher J. Farady
摘要
Activation of the NLRP3 inflammasome in response to danger signals is a key innate immune mechanism and results in the production of the pro-inflammatory cytokines interleukin-1β (IL-1β) and interleukin-18 (IL-18) as well as pyroptotic cell death. Aberrant NLRP3 activation has been linked to many acute and chronic conditions ranging from atherosclerosis to Alzheimer's disease and cancer, and based on the clinical success of IL-1-targeting therapies, NLRP3 has emerged as an attractive therapeutic target. Herein we describe our discovery, characterization, and structure-based optimization of a pyridazine-based series of NLRP3 inhibitors initiating from an high-throughput screening campaign. The scaffold, exemplified by lead molecule