炎症体
班级(哲学)
化学
药理学
业务
医学
计算机科学
生物化学
受体
人工智能
作者
Alexis Mollard,Devan Bursey,William J. Burnett,Taylor Avei,Benjamin Bearss,Ramesh Subbiah,Viduth K. Chaugule,Naga Srinivas Tripuraneni,Shipra Bijpuria,Russ Teichert,Chadwick T. Davis,Margit M. Janát‐Amsbury,Jared Bearss,David J. Bearss
标识
DOI:10.1080/1061186x.2025.2542856
摘要
, ofirnoflast exhibits oral bioavailability, achieving systemic exposures well above cellular potency thresholds. In a DSS-induced colitis model, treatment significantly reduces cytokine levels and improves phsyiological outcomes. Collectively, these findings validate NEK7 as a druggable checkpoint for NLRP3 inflammasome control and position Ofirnoflast as a mechanistically distinct, clinically advanced candidate for treating inflammation driven by aberrant inflammasome activation.
科研通智能强力驱动
Strongly Powered by AbleSci AI