赖氨酰氧化酶
化学
小分子
酶
IC50型
立体化学
分子
胺气处理
生物化学
体外
有机化学
作者
John H. Hutchinson,Martin W. Rowbottom,David Lonergan,Janice Darlington,Pat Prodanovich,Christopher D. King,Jilly F. Evans,Gretchen Bain
标识
DOI:10.1021/acsmedchemlett.7b00014
摘要
Two series of novel LOXL2 enzyme inhibitors are described: benzylamines substituted with electron withdrawing groups at the para-position and 2-substituted pyridine-4-ylmethanamines. The most potent compound, (2-chloropyridin-4-yl)methanamine 20 (hLOXL2 IC50 = 126 nM), was shown to be selective for LOXL2 over LOX and three other amine oxidases (MAO-A, MAO-B, and SSAO). Compound 20 is the first published small molecule inhibitor selective for LOXL2 over LOX.
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