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5-芳亚甲基硫代噻唑烷酮类作为酪氨酰 DNA 磷酸二酯酶 I 的抑制剂。

5-Arylidenethioxothiazolidinones as inhibitors of tyrosyl-DNA phosphodiesterase I.

机构信息

Center for Drug Design, Academic Health Center, University of Minnesota, Minneapolis, Minnesota 55455, USA.

出版信息

J Med Chem. 2012 Oct 25;55(20):8671-84. doi: 10.1021/jm3008773. Epub 2012 Oct 8.

Abstract

Tyrosyl-DNA phosphodiesterase I (Tdp1) is a cellular enzyme that repairs the irreversible topoisomerase I (Top1)-DNA complexes and confers chemotherapeutic resistance to Top1 inhibitors. Inhibiting Tdp1 provides an attractive approach to potentiating clinically used Top1 inhibitors. However, despite recent efforts in studying Tdp1 as a therapeutic target, its inhibition remains poorly understood and largely underexplored. We describe herein the discovery of arylidene thioxothiazolidinone as a scaffold for potent Tdp1 inhibitors based on an initial tyrphostin lead compound 8. Through structure-activity relationship (SAR) studies we demonstrated that arylidene thioxothiazolidinones inhibit Tdp1 and identified compound 50 as a submicromolar inhibitor of Tdp1 (IC₅₀ = 0.87 μM). Molecular modeling provided insight into key interactions essential for observed activities. Some derivatives were also active against endogenous Tdp1 in whole cell extracts. These findings contribute to advancing the understanding on Tdp1 inhibition.

摘要

酪氨酸-DNA 磷酸二酯酶 I(Tdp1)是一种细胞酶,可修复不可逆的拓扑异构酶 I(Top1)-DNA 复合物,并赋予 Top1 抑制剂抗药性。抑制 Tdp1 为增强临床使用的 Top1 抑制剂提供了一种有吸引力的方法。然而,尽管最近在研究 Tdp1 作为治疗靶标方面做了很多努力,但对其抑制作用的了解仍很差,而且在很大程度上尚未得到探索。我们在此描述了基于初始 tyrphostin 先导化合物 8,将芳基亚甲基噻唑烷-2,4-二酮作为有效 Tdp1 抑制剂的骨架的发现。通过构效关系(SAR)研究,我们证明芳基亚甲基噻唑烷-2,4-二酮抑制 Tdp1,并确定化合物 50 是 Tdp1 的亚微摩尔抑制剂(IC₅₀=0.87 μM)。分子建模提供了对观察到的活性至关重要的关键相互作用的深入了解。一些衍生物在全细胞提取物中对内源性 Tdp1 也具有活性。这些发现有助于深入了解 Tdp1 抑制作用。

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