Lee Jesang, Park Seung Bum
CRI Center for Chemical Proteomics, Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.
Department of Biophysics and Chemical Biology, Seoul National University, Seoul 08826, Republic of Korea.
Pharmaceuticals (Basel). 2022 Nov 27;15(12):1478. doi: 10.3390/ph15121478.
Recently, small-molecule covalent inhibitors have been accepted as a practical tool for targeting previously "undruggable" proteins. The high target selectivity of modern covalent inhibitors is now alleviating toxicity concerns regarding the covalent modifications of proteins. However, despite the tremendous clinical success of current covalent inhibitors, there are still unmet medical needs that covalent inhibitors have not yet addressed. This review categorized representative covalent inhibitors based on their mechanism of covalent inhibition: conventional covalent inhibitors, targeted covalent inhibitors (TCIs), and expanded TCIs. By reviewing both Food and Drug Administration (FDA)-approved drugs and drug candidates from recent literature, we provide insight into the future direction of covalent inhibitor development.
最近,小分子共价抑制剂已被公认为是一种针对先前“不可成药”蛋白质的实用工具。现代共价抑制剂的高靶点选择性正在缓解人们对蛋白质共价修饰毒性的担忧。然而,尽管目前的共价抑制剂在临床上取得了巨大成功,但仍有一些未满足的医疗需求是共价抑制剂尚未解决的。本综述根据其共价抑制机制对代表性共价抑制剂进行了分类:传统共价抑制剂、靶向共价抑制剂(TCI)和扩展TCI。通过回顾美国食品药品监督管理局(FDA)批准的药物以及近期文献中的候选药物,我们为共价抑制剂的未来发展方向提供了见解。