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Synthesis and structure-activity relationship of furoquinolinediones as inhibitors of Tyrosyl-DNA phosphodiesterase 2 (TDP2)

Journal 2018 · IF 4.816 · 发表于 2018 年 4 月 12 日
作者: Le-Mao Yu,Zhu Hu,Yu Chen,Azhar Ravji,Sophia Lopez,Caroline B. Plescia,Qian Yu,Hui Yang,Monica Abdelmalak,Sourav Saha,Keli Agama,Evgeny Kiselev,Christophe Marchand,Yves Pommier,Lin-Kun An
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摘要

Tyrosyl-DNA phosphodiesterase 2 (TDP2) is a recently discovered enzyme specifically repairing topoisomerase II (TOP2)-mediated DNA damage. It has been shown that inhibition of TDP2 synergize with TOP2 inhibitors . Herein, we report the discovery of the furoquinolinedione chemotype as a suitable skeleton for the development of selective TDP2 inhibitors. Compound 1 was identified as a TDP2 inhibitor as a result of screening our in-house compound library for compounds selective for TDP2 vs. TDP1 . Further SAR studies provide several selective TDP2 inhibitors at low-micromolar range. The most potent compound 74 shows inhibitory activity with IC 50 of 1.9 and 2.1 μM against recombinant TDP2 and TDP2 in whole cell extracts (WCE), respectively.