锡克
化学
赫尔格
药理学
酪氨酸激酶
激酶
布鲁顿酪氨酸激酶
酪氨酸激酶抑制剂
原癌基因酪氨酸蛋白激酶Src
生物化学
信号转导
钾通道
内科学
医学
癌症
作者
John Liddle,Francis Atkinson,Michael D. Barker,Paul S. Carter,Neil R. Curtis,Rob P. Davis,Clement Douault,Marion C. Dickson,Dorothy Elwes,Neil Garton,Matthew Gray,Thomas G. Hayhow,Clare I. Hobbs,Emma J. Jones,S. Leach,Karen Leavens,Huw D. Lewis,Scott McCleary,Margarete Neu,Vipulkumar K. Patel
标识
DOI:10.1016/j.bmcl.2011.07.082
摘要
The lead optimisation of the diaminopyrimidine carboxamide series of spleen tyrosine kinase inhibitors is described. The medicinal chemistry strategy was focused on optimising the human whole blood activity whilst achieving a sufficient margin over liability kinases and hERG activity. GSK143 is a potent and highly selective SYK inhibitor showing good efficacy in the rat Arthus model.
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