N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, 9, Akademika Lavrentieva Ave., Novosibirsk 630090, Russia.
Department of Natural Sciences and Institute of Medicine and Psychology, Novosibirsk State University, Pirogova 2, Novosibirsk 630090, Russia.
Molecules. 2018 Sep 26;23(10):2468. doi: 10.3390/molecules23102468.
Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is a DNA repair enzyme that mends topoisomerase 1-mediated DNA damage. Tdp1 is a current inhibition target for the development of improved anticancer treatments, as its inhibition may enhance the therapeutic effect of topoisomerase 1 poisons. Here, we report a study on the development of a novel class of Tdp1 inhibitors that is based on the octahydro-2-chromene scaffold. Inhibition and binding assays revealed that these compounds are potent inhibitors of Tdp1, with IC and values in the low micromolar concentration range. Molecular modelling predicted plausible conformations of the active ligands, blocking access to the enzymatic machinery of Tdp1. Our results thus help establish a structural-activity relationship for octahydro-2-chromene-based Tdp1 inhibitors, which will be useful for future Tdp1 inhibitor development work.
酪氨酰 DNA 磷酸二酯酶 1(Tdp1)是一种修复酶,可修复拓扑异构酶 1 介导的 DNA 损伤。Tdp1 是目前开发改进的抗癌治疗方法的抑制靶点,因为其抑制作用可能增强拓扑异构酶 1 毒物的治疗效果。在这里,我们报告了一类新型 Tdp1 抑制剂的开发研究,该抑制剂基于八氢-2-色烯骨架。抑制和结合实验表明,这些化合物是 Tdp1 的有效抑制剂,IC 和 值在低微摩尔浓度范围内。分子建模预测了活性配体的合理构象,阻止了它们进入 Tdp1 的酶机制。因此,我们的研究结果为八氢-2-色烯基 Tdp1 抑制剂建立了构效关系,这将有助于未来的 Tdp1 抑制剂开发工作。