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首页> 外文期刊>Chimia >Contribution to the Discovery of a Novel Medicine for a Neuromuscular Disease and of other Promising Molecules for the Treatment of Neurodevelopmental and Neurodegenerative Diseases
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Contribution to the Discovery of a Novel Medicine for a Neuromuscular Disease and of other Promising Molecules for the Treatment of Neurodevelopmental and Neurodegenerative Diseases

机译:对神经肌病疾病的新药和其他有前途分子的贡献,用于治疗神经发育和神经变性疾病

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摘要

Nervous system disorders affect millions of people around the world, through a very broad range of diseases. Here we describe our contribution to find a treatment for patients suffering from three of those diseases. The first one, autism spectrum disorder (ASD), affects approximately one in every 59 children in US. The second one, spinal muscular atrophy (SMA) is a rare disease affecting 1 in 10000 live births worldwide, often leading to death if untreated. The third one, Alzheimer's disease (AD) is a very well known devastating disease with an estimated 50 million people living with AD and other dementia, a number expected to triple by 2050. Our strategy to address those diseases was directed towards the discovery of a selective vasopressin 1 a (V1 a) antagonist for ASD, a splicing modifier of the survival of motor neuron 2 (SMN2) for SMA, and finally a γ-secretase modulator (GSM) for AD. In the frame of our GSM project, we also reported the discovery of a bridge piperidine moiety as a bioisostere for a phenyl moiety with an improved drug-like profile.
机译:神经系统疾病通过广泛的疾病影响全世界数百万人。在这里,我们描述了我们对患有三种疾病的患者进行治疗的贡献。第一个,自闭症谱系障碍(ASD),在美国每59名儿童中大约影响大约一个人。第二个,脊柱肌肉萎缩(SMA)是一种罕见的疾病,在全世界10000个活产出生中影响1,往往导致死亡,如果未经治疗。第三个,阿尔茨海默病(AD)是一种非常令人着迷的毁灭性疾病,估计有5000万人与广告和其他痴呆症,预计到2050年的人数预计。我们解决这些疾病的战略是针对一个用于ASD的选择性血管加压素1A(V1a)拮抗剂,SMA的运动神经元2(SMN2)的存活改性剂,最后是AD的γ-分泌酶调节剂(GSM)。在我们的GSM项目的框架中,我们还报告了将桥哌啶部分的发现作为生物偏见的苯基部分,其具有改进的药物样曲线。

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