1. Academic Validation
  2. Characterization of a small molecule inhibitor of the NLRP3 inflammasome and its potential use for acute lung injury

Characterization of a small molecule inhibitor of the NLRP3 inflammasome and its potential use for acute lung injury

  • Bioorg Chem. 2024 Sep:150:107562. doi: 10.1016/j.bioorg.2024.107562.
Yiming Xu 1 Savannah Biby 1 Chunqing Guo 2 Zheng Liu 2 Jinyang Cai 2 Xiang-Yang Wang 2 Shijun Zhang 3
Affiliations

Affiliations

  • 1 Department of Medicinal Chemistry, Virginia Commonwealth University, Richmond, VA 23298, USA.
  • 2 Department of Human and Molecular Genetics, Virginia Commonwealth University, Richmond, VA 23298, USA.
  • 3 Department of Medicinal Chemistry, Virginia Commonwealth University, Richmond, VA 23298, USA. Electronic address: szhang2@vcu.edu.
Abstract

Accumulating data support the key roles of the NLRP3 inflammasome, an essential component of the innate immune system, in human pathophysiology. As an emerging drug target and a potential biomarker for human diseases, small molecule inhibitors of the NLRP3 inflammasome have been actively pursued. Our recent studies identified a small molecule, MS-II-124, as a potent NLRP3 Inhibitor and potential imaging probe. In this report, MS-II-124 was further characterized by an unbiased and comprehensive analysis through Eurofins BioMAP Diversity PLUS panel that contains 12 human primary cell-based systems. The analysis revealed promising activities of MS-II-124 on inflammation and immune functions, further supporting the roles of the NLRP3 inflammasome in these model systems. Further studies of MS-II-124 in mouse model of acute lung injury (ALI)/acute respiratory distress syndrome (ARDS) and NLRP3 knockout mice demonstrated its target engagement, efficacy to suppress inflammatory cytokines and infiltration of immune cells in the lung tissues. In summary, the results support the therapeutic potential of MS-II-124 as a NLRP3 Inhibitor and warrant future studies of this compound and its analogs to develop therapeutics for ALI/ARDS.

Keywords

Acute lung injury (ALI)/acute respiratory distress syndrome (ARDS); BioMAP; Infiltration; Inflammatory cytokines; Inhibitor; NLRP3 inflammasome.

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