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发现新型强效和高选择性糖原合酶激酶-3β(GSK3β)抑制剂用于治疗阿尔茨海默病:吡嗪类化合物的设计、合成与表征。

Discovery of novel potent and highly selective glycogen synthase kinase-3β (GSK3β) inhibitors for Alzheimer's disease: design, synthesis, and characterization of pyrazines.

机构信息

Department of Medicinal Chemistry, AstraZeneca R&D, Innovative Medicines CNS & Pain Södertälje, SE-151 85 Södertälje, Sweden.

出版信息

J Med Chem. 2012 Nov 8;55(21):9107-19. doi: 10.1021/jm201724m. Epub 2012 Apr 27.

Abstract

Glycogen synthase kinase-3β, also called tau phosphorylating kinase, is a proline-directed serine/threonine kinase which was originally identified due to its role in glycogen metabolism. Active forms of GSK3β localize to pretangle pathology including dystrophic neuritis and neurofibrillary tangles in Alzheimer's disease (AD) brain. By using a high throughput screening (HTS) approach to search for new chemical series and cocrystallization of key analogues to guide the optimization and synthesis of our pyrazine series, we have developed highly potent and selective inhibitors showing cellular efficacy and blood-brain barrier penetrance. The inhibitors are suitable for in vivo efficacy testing and may serve as a new treatment strategy for Alzheimer's disease.

摘要

糖原合酶激酶-3β,也称为 tau 磷酸化激酶,是一种脯氨酸导向的丝氨酸/苏氨酸激酶,最初因其在糖原代谢中的作用而被发现。GSK3β 的活性形式定位于 pretangle 病理学中,包括阿尔茨海默病(AD)大脑中的神经纤维缠结和神经原纤维缠结。通过使用高通量筛选(HTS)方法来搜索新的化学系列和关键类似物的共结晶来指导我们的吡嗪系列的优化和合成,我们已经开发出高效且选择性的抑制剂,显示出细胞功效和血脑屏障通透性。这些抑制剂适合进行体内疗效测试,并可能成为阿尔茨海默病的新治疗策略。

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