| Literature DB >> 25469863 |
Timothy D Cushing1, Xiaolin Hao, Youngsook Shin, Kristin Andrews, Matthew Brown, Mario Cardozo, Yi Chen, Jason Duquette, Ben Fisher, Felix Gonzalez-Lopez de Turiso, Xiao He, Kirk R Henne, Yi-Ling Hu, Randall Hungate, Michael G Johnson, Ron C Kelly, Brian Lucas, John D McCarter, Lawrence R McGee, Julio C Medina, Tisha San Miguel, Deanna Mohn, Vatee Pattaropong, Liping H Pettus, Andreas Reichelt, Robert M Rzasa, Jennifer Seganish, Andrew S Tasker, Robert C Wahl, Sharon Wannberg, Douglas A Whittington, John Whoriskey, Gang Yu, Leeanne Zalameda, Dawei Zhang, Daniela P Metz.
Abstract
The development and optimization of a series of quinolinylpurines as potent and selective PI3Kδ kinase inhibitors with excellent physicochemical properties are described. This medicinal chemistry effort led to the identification of 1 (AMG319), a compound with an IC50 of 16 nM in a human whole blood assay (HWB), excellent selectivity over a large panel of protein kinases, and a high level of in vivo efficacy as measured by two rodent disease models of inflammation.Entities:
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Year: 2014 PMID: 25469863 DOI: 10.1021/jm501624r
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446