Lapshina Maria A, Shevtsova Elena F, Grigoriev Vladimir V, Aksinenko Aleksey Yu, Ustyugov Aleksey A, Steinberg Daniil A, Maleev Grigoriy V, Dubrovskaya Elena S, Goreva Tatiana V, Epishina Tatiana A, Zamoyski Vladimir L, Makhaeva Galina F, Fisenko Vladimir P, Veselov Ivan M, Vinogradova Daria V, Bachurin Sergey O
Institute of Physiologically Active Compounds at the Federal Research Center of Problems of Chemical Physics and Medicinal Chemistry, Russian Academy of Sciences, 1 Severnij proezd, 142432 Chernogolovka, Russia.
Department of Pharmacology, Sechenov I. M. First Moscow State Medical University, 8 Build. 2 Trubetskaya Str., 119991 Moscow, Russia.
Molecules. 2023 Nov 13;28(22):7567. doi: 10.3390/molecules28227567.
Currently, there are no effective drugs for the treatment of amyotrophic lateral sclerosis (ALS). Only two drugs-edaravone and riluzole-have been approved, but they have very limited efficacy. The aim of this work was to modify the structural core of the Edaravone-phenylpyrazolone moiety and combine it with aminoadamantane pharmacophore in order to expand the spectrum of its action to a number of processes involved in the pathogenesis of ALS. New conjugates of edaravone derivatives with 1-aminoadamantanes combined with alkylene or hydroxypropylene spacers were synthesized, and their biological activity was investigated. Compounds were found that could inhibit lipid peroxidation and calcium-related mitochondrial permeability, block fast sodium currents of CNS neurons, and reduce aggregation of the mutated form of the FUS-protein typical to ALS. So, the proposed modification of the edaravone molecule has allowed the obtaining of new original structures that combine some prospective therapeutic mechanisms against key chains of the pathogenesis of ALS. The identified lead compounds can be used for further optimization and development of new promising drugs on this basis for the treatment of ALS.
目前,尚无治疗肌萎缩侧索硬化症(ALS)的有效药物。仅有两种药物——依达拉奉和利鲁唑——已获批准,但它们的疗效非常有限。这项工作的目的是修饰依达拉奉的结构核心——苯基吡唑啉酮部分,并将其与氨基金刚烷药效基团结合,以将其作用谱扩展至ALS发病机制涉及的多个过程。合成了依达拉奉衍生物与1-氨基金刚烷通过亚烷基或羟亚丙基间隔基连接的新型缀合物,并对其生物活性进行了研究。发现这些化合物能够抑制脂质过氧化和与钙相关的线粒体通透性,阻断中枢神经系统神经元的快速钠电流,并减少ALS典型的FUS蛋白突变形式的聚集。因此,对依达拉奉分子的拟议修饰已使得获得了新的原始结构,这些结构结合了一些针对ALS发病机制关键环节的潜在治疗机制。在此基础上,所鉴定的先导化合物可用于进一步优化和开发治疗ALS的新的有前景的药物。