药物发现
药理学
小分子
敌手
受体
受体拮抗剂
转基因小鼠
阿尔茨海默病
药品
疾病
医学
转基因
神经科学
化学
生物
生物信息学
内科学
生物化学
基因
作者
Gilbert M. Rishton,Gary C. Look,Zhi‐Jie Ni,Jason Zhang,Yingcai Wang,Yaodong Huang,Xiaodong Wu,Nicholas J. Izzo,Kelsie M. LaBarbera,Colleen S. Limegrover,Courtney Rehak,Raymond Yurko,Susan M. Catalano
标识
DOI:10.1021/acsmedchemlett.1c00048
摘要
An unbiased phenotypic neuronal assay was developed to measure the synaptotoxic effects of soluble Aβ oligomers. A collection of CNS druglike small molecules prepared by conditioned extraction was screened. Compounds that prevented and reversed synaptotoxic effects of Aβ oligomers in neurons were discovered to bind to the sigma-2 receptor complex. Select development compounds displaced receptor-bound Aβ oligomers, rescued synapses, and restored cognitive function in transgenic hAPP Swe/Ldn mice. Our first-in-class orally administered small molecule investigational drug 7 (CT1812) has been advanced to Phase II clinical studies for Alzheimer's disease.
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