Novartis Institutes for BioMedical Research , 250 Massachusetts Avenue , Cambridge , Massachusetts 02139 , United States.
Novartis Pharmaceuticals , 250 Massachusetts Avenue , Cambridge , Massachusetts 02139 , United States.
J Med Chem. 2018 Dec 27;61(24):11021-11036. doi: 10.1021/acs.jmedchem.8b01291. Epub 2018 Dec 13.
Spinal muscular atrophy (SMA), a rare neuromuscular disorder, is the leading genetic cause of death in infants and toddlers. SMA is caused by the deletion or a loss of function mutation of the survival motor neuron 1 (SMN1) gene. In humans, a second closely related gene SMN2 exists; however it codes for a less stable SMN protein. In recent years, significant progress has been made toward disease modifying treatments for SMA by modulating SMN2 pre-mRNA splicing. Herein, we describe the discovery of LMI070/branaplam, a small molecule that stabilizes the interaction between the spliceosome and SMN2 pre-mRNA. Branaplam (1) originated from a high-throughput phenotypic screening hit, pyridazine 2, and evolved via multiparameter lead optimization. In a severe mouse SMA model, branaplam treatment increased full-length SMN RNA and protein levels, and extended survival. Currently, branaplam is in clinical studies for SMA.
脊髓性肌萎缩症(SMA)是一种罕见的神经肌肉疾病,是婴儿和幼儿死亡的主要遗传原因。SMA 是由生存运动神经元 1(SMN1)基因的缺失或功能丧失突变引起的。在人类中,存在第二个密切相关的基因 SMN2;然而,它编码的是一种不太稳定的 SMN 蛋白。近年来,通过调节 SMN2 前体 mRNA 的剪接,在 SMA 的疾病修饰治疗方面取得了重大进展。本文描述了小分子 LMI070/branaplam 的发现,它稳定了剪接体和 SMN2 前体 mRNA 之间的相互作用。branaplam(1)源自高通量表型筛选命中物嘧啶 2,并通过多参数先导优化进化而来。在严重的小鼠 SMA 模型中,branaplam 治疗增加了全长 SMN RNA 和蛋白水平,并延长了生存时间。目前,branaplam 正在进行 SMA 的临床研究。