Department of Therapeutic Discovery, ‡Department of Pharmacokinetics and Drug Metabolism, and §Department of Pharmaceutics Research and Development, Amgen Inc. , 1120 Veterans Boulevard, South San Francisco, California 94080, United States.
J Med Chem. 2015 Jan 8;58(1):480-511. doi: 10.1021/jm501624r. Epub 2014 Dec 3.
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.
本文描述了一系列喹啉基嘌呤作为有效和选择性 PI3Kδ 激酶抑制剂的开发和优化,这些化合物具有优异的物理化学性质。通过这项药物化学研究,发现了化合物 1(AMG319),在人全血测定(HWB)中其 IC50 为 16 nM,对一大类蛋白激酶具有优异的选择性,并且在两种炎症的啮齿动物疾病模型中具有较高的体内疗效。