Department of Chemistry, Texas A&M University, Corner of Ross and Spence Streets, College Station, TX, 77843, USA.
ChemMedChem. 2019 May 6;14(9):889-906. doi: 10.1002/cmdc.201900107. Epub 2019 Mar 26.
Although covalent inhibitors have been used as therapeutics for more than a century, there has been general resistance in the pharmaceutical industry against their further development due to safety concerns. This inclination has recently been reverted after the development of a wide variety of covalent inhibitors to address human health conditions along with the US Food and Drug Administration (FDA) approval of several covalent therapeutics for use in humans. Along with this exciting resurrection of an old drug discovery concept, this review surveys enzymes that can be targeted by covalent inhibitors for the treatment of human diseases. We focus on protein kinases, RAS proteins, and a few other enzymes that have been studied extensively as targets for covalent inhibition, with the aim to address challenges in designing effective covalent drugs and to provide suggestions in the area that have yet to be explored.
虽然共价抑制剂作为治疗药物已经使用了一个多世纪,但由于安全问题,制药行业普遍反对进一步开发它们。这种倾向在开发出各种各样的共价抑制剂来解决人类健康问题以及美国食品和药物管理局 (FDA) 批准几种共价疗法用于人类之后,最近发生了逆转。随着这一古老药物发现概念的令人兴奋的复兴,本综述调查了可通过共价抑制剂靶向的酶,以治疗人类疾病。我们专注于蛋白激酶、RAS 蛋白和其他一些已被广泛研究作为共价抑制靶点的酶,旨在解决有效共价药物设计方面的挑战,并为尚未探索的领域提供建议。