Design and synthesis of selective imidazo[1,2-b]pyridazine and pyrazolo[1,5-a]pyrimidine inhibitors of leucine-rich repeat kinase 2 (LRRK2) using a checkpoint kinase 1 (CHK1)-derived crystallographic surrogate

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作者：
Ray, Stuart [1 ]
机构：
[1] Vernalis, Chem, Cambridge, Great Abington, England
来源：
ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 2018年 / 256卷
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中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
53
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页数：1
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