Department of Pharmaceutical Engineering & Department of Biochemical Engineering, School of Engineering, China Pharmaceutical University, 639 Longmian Avenue, Nanjing 211198, PR China.
Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, PR China.
Future Med Chem. 2018 Apr 1;10(8):907-934. doi: 10.4155/fmc-2017-0207. Epub 2018 Apr 12.
Sirtuins (SIRT) are coenzyme NAD-dependent histone deacetylases for the transfer of modified acetyl groups. Sirtuins are widely involved in various physiological processes and therefore associated with cardiovascular disease, diabetes, Parkinson's disease, cancer and beyond. Consequently, the development of modulators for sirtuins has considerable clinical value. To date, a variety of SIRT1/2 inhibitors have been reported and none has been approved for the market. This review summarizes the recent progress in the discovery and development of SIRT1/2 inhibitors including their inhibitory potency, structure-activity relationship and binding mode analysis as well as discusses the perspective for the future development of SIRT1/2 inhibitors.
Sirtuins(SIRT)是辅酶 NAD 依赖性组蛋白去乙酰化酶,用于转移修饰的乙酰基。Sirtuins 广泛参与各种生理过程,因此与心血管疾病、糖尿病、帕金森病、癌症等有关。因此,开发 Sirtuins 的调节剂具有相当大的临床价值。迄今为止,已经报道了多种 SIRT1/2 抑制剂,但没有一种被批准上市。本综述总结了 SIRT1/2 抑制剂的发现和开发的最新进展,包括它们的抑制活性、构效关系和结合模式分析,并讨论了 SIRT1/2 抑制剂未来发展的前景。