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,Alex Preston,César Ramírez-Molina,Tracy J. Shipley,Philip A. Skone,Nick Smithers,D.O. Somers,Ann L. Walker,Robert J. Watson,Gordon G. Weingarten
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.