正电子发射断层摄影术
化学
神经退行性变
示踪剂
发射计算机断层扫描
核磁共振
神经科学
物理
疾病
内科学
心理学
核物理学
医学
作者
Frederik Rombouts,Lieven Declercq,José-Ignacio Andrés,Astrid Bottelbergs,Lu Chen,Laura Iturrino,Joseph E. Leenaerts,Jonas Mariën,Fengfei Song,Cindy Wintmolders,Stijn Wuyts,Chunfang Xia,Paula te Riele,Guy Bormans,Rik Vandenberghe,Hartmuth C. Kolb,Diederik Moechars
标识
DOI:10.1021/acs.jmedchem.8b01759
摘要
In Alzheimer's disease, the density and spread of aggregated tau protein track well with neurodegeneration and cognitive decline, making the imaging of aggregated tau a compelling biomarker. A structure-activity relationship exploration around an isoquinoline hit, followed by an exploration of tolerated fluorination positions, allowed us to identify 9 (JNJ-64326067), a potent and selective binder to aggregated tau with a favorable pharmacokinetic profile and no apparent off-target binding. This was confirmed in rat and monkey positron emission tomography studies using [18F]9.
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