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(S)-N-(1-(7-氟-2-(吡啶-2-基)喹啉-3-基)乙基)-9H-嘌呤-6-胺(AMG319)及相关 PI3Kδ抑制剂的发现及在炎症和自身免疫性疾病中的体内评价。

Discovery and in vivo evaluation of (S)-N-(1-(7-fluoro-2-(pyridin-2-yl)quinolin-3-yl)ethyl)-9H-purin-6-amine (AMG319) and related PI3Kδ inhibitors for inflammation and autoimmune disease.

机构信息

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.

出版信息

J Med Chem. 2015 Jan 8;58(1):480-511. doi: 10.1021/jm501624r. Epub 2014 Dec 3.

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.

摘要

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。

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