Dai Pengcheng, Xin Yufeng, Qin Xiuting, Ma Hao, Zhuang Chunlin
School of Pharmacy, Guangdong Pharmaceutical University, Guangzhou 510006, China.
School of Pharmacy, Ningxia Medical University, Yinchuan 750004, China.
Bioorg Med Chem. 2025 Oct 1;128:118246. doi: 10.1016/j.bmc.2025.118246. Epub 2025 May 19.
Necroptosis is a highly regulated form of cell death. Mixed lineage kinase domain-like protein (MLKL) serves as its central effector and plays a critical role in various physiological and pathological processes. Given its close association with multiple diseases, MLKL has emerged as a promising therapeutic target. This review highlights recent advances in the development of necroptosis inhibitors and degraders targeting MLKL. The optimization of active compounds, structural modifications, and the applications of proteolysis-targeting chimeras (PROTACs) are emphasized. Furthermore, this study systematically evaluates the structural characteristics and biological activities of these compounds, thereby providing critical insights to inform future investigations and pharmaceutical development within this field.
坏死性凋亡是一种高度受调控的细胞死亡形式。混合谱系激酶结构域样蛋白(MLKL)作为其核心效应器,在各种生理和病理过程中发挥关键作用。鉴于其与多种疾病密切相关,MLKL已成为一个有前景的治疗靶点。本综述重点介绍了针对MLKL的坏死性凋亡抑制剂和降解剂开发的最新进展。强调了活性化合物的优化、结构修饰以及蛋白酶靶向嵌合体(PROTACs)的应用。此外,本研究系统评估了这些化合物的结构特征和生物活性,从而为该领域未来的研究和药物开发提供关键见解。