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新型嘧啶-4-基-乙醇衍生物的合成及生物评价作为 ROS1 激酶抑制剂。

Synthesis and biological evaluation of new pyrimidine-4-yl-ethanol derivatives as ROS1 kinase inhibitors.

机构信息

Department of Biological Chemistry, Korea University of Science and Technology , Gwahangno, Yuseong-gu, Daejeon , Republic of Korea and.

出版信息

J Enzyme Inhib Med Chem. 2015 Apr;30(2):290-8. doi: 10.3109/14756366.2014.920838. Epub 2014 Jun 18.

Abstract

As a part of trials to target ROS1 kinase with potential inhibitors, a novel series of pyrimidin-4-yl-ethanol and ethanone derivatives (4a-f, 5a-f, 6a-f and 7a-f) have been designed based on previously discovered lead compounds KIST301072 and KIST301080, and synthesized on 4-5 steps according to compounds. The structures of the newly synthesized compounds have been confirmed on (1)H-NMR, (13)C-NMR and IR. Most of the tested compounds showed ROS1 kinase inhibitory activity in micromolar range.

摘要

作为以潜在的 ROS1 激酶抑制剂为靶点的试验的一部分,根据先前发现的先导化合物 KIST301072 和 KIST301080,设计了一系列新的嘧啶-4-基-乙醇和乙酮衍生物(4a-f、5a-f、6a-f 和 7a-f),并根据化合物在 4-5 步进行合成。新合成的化合物的结构已通过(1)H-NMR、(13)C-NMR 和 IR 得到证实。大多数测试的化合物在微摩尔范围内显示出 ROS1 激酶抑制活性。

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