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合成一个芳氧基氧代嘧啶酮文库,该文库显示出对 ALK 的选择性抑制作用。

Synthesis of an aryloxy oxo pyrimidinone library that displays ALK-selective inhibition.

机构信息

Department of Chemical Biology and Therapeutics, St. Jude Children's Research Hospital, Memphis, TN 38105-3678, United States.

出版信息

Bioorg Med Chem Lett. 2011 Aug 1;21(15):4592-6. doi: 10.1016/j.bmcl.2011.05.103. Epub 2011 Jun 12.

Abstract

We report the synthesis of a pyrimidinone library that targets anaplastic lymphoma kinase (ALK), an oncogenic receptor tyrosine kinase. This library was generated in three steps from a versatile commercially available starting material. Some compounds within this library showed single digit micromolar inhibition of ALK in vitro, while showing minimal inhibition of other homologous insulin receptor family kinases including the human insulin receptor kinase (IRK), at the highest concentrations investigated. We also present initial ALK structure-activity relationships for this library.

摘要

我们报告了一种嘧啶酮文库的合成,该文库针对间变性淋巴瘤激酶(ALK),一种致癌受体酪氨酸激酶。该文库由一种多功能的商业上可获得的起始原料经过三步合成得到。该文库中的一些化合物在体外对 ALK 的抑制作用达到个位数微摩尔,而在最高浓度下对其他同源胰岛素受体家族激酶(包括人胰岛素受体激酶(IRK))的抑制作用最小。我们还提出了该文库的初步 ALK 结构活性关系。

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