Structural Optimization of Benzyl-5-methyl-1 H -Imidazole Derivatives as Human Glutaminyl Cyclase Inhibitors

作者：Yu-Ting Chen, Fanbo Meng, Yu-Qing Zhuang, Ziyang Chen, Yao-Geng Wang, Xiang-Li Ning, W. Liu, Rong Li, Hua-li Wang, G. Li · 发表于：ACS Medicinal Chemistry Letters · 年份：2026 · DOI：10.1021/acsmedchemlett.6c00028 · 研究领域：Cancer, Hypoxia, and Metabolism、Glycosylation and Glycoproteins Research、Amino Acid Enzymes and Metabolism

Human secretory glutaminyl cyclase (sQC) and Golgi-resident glutaminyl cyclase (gQC) catalyze the conversion of protein N-terminal glutamine into pyroglutamate (pE), a modification implicated in human diseases including cancer. Small-molecule inhibitors targeting sQC/gQC represent a promising therapeutic strategy. Here, we report a series of benzyl-5-methyl-1 H -imidazole derivatives as inhibitors of sQC/gQC. Through structural optimization, we identified CL121, a nanomolar potent inhibitor of both enzymes. Thermal shift assays revealed that CL121 enhances the thermal stability of both sQC (Δ T m = 5.9 °C) and gQC (Δ T m = 6.0 °C), indicating strong binding interactions. Cellular assays revealed that CL121 substantially reduced the level of pE-CD47 modification on the surface of MDA-MB-231 and KYSE30 cells. Furthermore, CL121 exhibited antitumor activity in a mouse xenograft tumor model. The results highlight the potential of CL121 as a lead compound for developing drugs targeting sQC/gQC-mediated diseases.