European Journal of Medicinal Chemistry p. 777 - 796 (2018)
Update date:2022-08-29
Topics:
Yu, Le-Mao
Hu, Zhu
Chen, Yu
Ravji, Azhar
Lopez, Sophia
Plescia, Caroline B.
Yu, Qian
Yang, Hui
Abdelmalak, Monica
Saha, Sourav
Agama, Keli
Kiselev, Evgeny
Marchand, Christophe
Pommier, Yves
An, Lin-Kun
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 IC50 of 1.9 and 2.1 μM against recombinant TDP2 and TDP2 in whole cell extracts (WCE), respectively.
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