Calder Alyssa N, Androphy Elliot J, Hodgetts Kevin J
Laboratory for Drug Discovery in Neurodegeneration, Brigham & Women's Hospital and Harvard Medical School , 65 Landsdowne Street, Cambridge, Massachusetts 02139, United States.
Department of Dermatology, Indiana University School of Medicine , Indianapolis, Indiana 46202, United States.
J Med Chem. 2016 Nov 23;59(22):10067-10083. doi: 10.1021/acs.jmedchem.6b00670. Epub 2016 Aug 16.
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease resulting from pathologically low levels of survival motor neuron (SMN) protein. The majority of mRNA from the SMN2 allele undergoes alternative splicing and excludes critical codons, causing an SMN protein deficiency. While there is currently no FDA-approved treatment for SMA, early therapeutic efforts have focused on testing repurposed drugs such as phenylbutyrate (2), valproic acid (3), riluzole (6), hydroxyurea (7), and albuterol (9), none of which has demonstrated clinical effectiveness. More recently, clinical trials have focused on novel small-molecule compounds identified from high-throughput screening and medicinal chemistry optimization such as olesoxime (11), CK-2127107, RG7800, LMI070, and RG3039 (17). In this paper, we review both repurposed drugs and small-molecule compounds discovered following medicinal chemistry optimization for the potential treatment of SMA.
脊髓性肌萎缩症(SMA)是一种常染色体隐性神经退行性疾病,由生存运动神经元(SMN)蛋白的病理性低水平所致。SMN2等位基因的大部分mRNA会进行可变剪接并排除关键密码子,导致SMN蛋白缺乏。虽然目前美国食品药品监督管理局(FDA)尚未批准用于治疗SMA的药物,但早期的治疗尝试集中在测试如苯丁酸钠(2)、丙戊酸(3)、利鲁唑(6)、羟基脲(7)和沙丁胺醇(9)等重新利用的药物,然而这些药物均未显示出临床疗效。最近,临床试验集中在从高通量筛选和药物化学优化中鉴定出的新型小分子化合物上,如油肟酸(11)、CK - 2127107、RG7800、LMI070和RG3039(17)。在本文中,我们综述了重新利用的药物以及经药物化学优化后发现的用于潜在治疗SMA的小分子化合物。