Department of Chemistry , Vanderbilt University , Nashville , Tennessee 37232-0146 , United States.
J Med Chem. 2018 Jul 26;61(14):6002-6017. doi: 10.1021/acs.jmedchem.8b00360. Epub 2018 Jul 11.
Deregulated RAS activity, often the result of mutation, is implicated in approximately 30% of all human cancers. Despite this statistic, no clinically successful treatment for RAS-driven tumors has yet been developed. One approach for modulating RAS activity is to target and affect the activity of proteins that interact with RAS, such as the guanine nucleotide exchange factor (GEF) son of sevenless homologue 1 (SOS1). Here, we report on structure-activity relationships (SAR) in an indole series of compounds. Using structure-based design, we systematically explored substitution patterns on the indole nucleus, the pendant amino acid moiety, and the linker unit that connects these two fragments. Best-in-class compounds activate the nucleotide exchange process at submicromolar concentrations in vitro, increase levels of active RAS-GTP in HeLa cells, and elicit signaling changes in the mitogen-activated protein kinase-extracellular regulated kinase (MAPK-ERK) pathway, resulting in a decrease in pERK1/2 protein levels at higher compound concentrations.
RAS 活性失调通常是突变的结果,约占所有人类癌症的 30%。尽管有这一统计数据,但尚未开发出针对 RAS 驱动肿瘤的临床有效治疗方法。调节 RAS 活性的一种方法是靶向并影响与 RAS 相互作用的蛋白质的活性,例如鸟嘌呤核苷酸交换因子(GEF)son of sevenless homologue 1(SOS1)。在这里,我们报告了吲哚系列化合物的构效关系(SAR)。我们使用基于结构的设计,系统地探索了吲哚核、侧链氨基酸部分和连接这两个片段的连接单元上的取代模式。最佳类别的化合物以亚微摩尔浓度在体外激活核苷酸交换过程,增加 HeLa 细胞中活性 RAS-GTP 的水平,并在丝裂原激活的蛋白激酶-细胞外调节激酶(MAPK-ERK)途径中引起信号变化,导致较高化合物浓度下 pERK1/2 蛋白水平降低。