化学
连接器
泛素连接酶
乳腺癌
细胞内
癌症治疗
生物化学
酶
癌症研究
药理学
细胞外
烟酰胺
靶蛋白
点击化学
配体(生物化学)
蛋白质降解
烟酰胺磷酸核糖转移酶
DNA连接酶
癌症
评论文章
计算生物学
药物发现
癌症治疗
作者
Ubaldina Galli,Marianna Moro,Federica Carolina Balestrero,Giorgia Colombo,Marco Koten,Benedetta Roncaglio,Armando A. Genazzani,Silvio Aprile,Alberto Massarotti,Giuseppe Orsomando,Tracey Pirali,Ambra A. Grolla
标识
DOI:10.1021/acs.jmedchem.5c01827
摘要
High Resolution Image Download MS PowerPoint Slide PROTACs (proteolysis-targeting chimeras) enable selective protein degradation through the ubiquitin–proteasome system and offer opportunities to target moonlighting proteins with nonenzymatic functions. We report the design, synthesis, and biological evaluation of NAMPT-directed PROTACs derived from our previously described inhibitor MV78 ( 7 ). A modular click chemistry strategy facilitated rapid assembly of a focused library by varying linker architectures and E3 ligase recruiters, with emphasis on the impact of a triazole unit. Structure–activity relationship studies revealed that eliminating the triazole from the linker and introducing an ( S )-methyl group on the VHL ligand markedly enhanced degradation. The optimized degrader, U42, exhibited low nanomolar antiproliferative activity, robust intracellular and extracellular NAMPT degradation, excellent metabolic stability, favorable pharmacokinetics, and sustained efficacy in mammosphere models, three-dimensional breast cancer cultures not previously explored with NAMPT degraders. These findings highlight U42 as a lead compound and provide strong rationale for advancing NAMPT-directed PROTACs as a therapeutic strategy in breast cancer.
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