Discovery of dihydrospiro[cyclopropane-1,7′-pyrrolo[3,4-d]pyrimidine] derivatives as novel ATR inhibitors

Abstract

Ataxia telangiectasia and Rad3-related (ATR) kinase plays a critical role in the DNA damage response (DDR), making it a promising target for cancer therapy. Herein, a series of dihydrospiro[cyclopropane-1,7′-pyrrolo[3,4-d]pyrimidine] derivatives have been identified as a novel class of ATR inhibitors. Among them, compound 10h exhibited the most excellent ATR kinase inhibitory activity, with an IC50 value of 6.89 nM. In vitro, 10h demonstrated potent anti-tumor activity and effectively inhibited niraparib-induced CHK1 phosphorylation in Granta-519. Pairwise drug combinational antiproliferative assays revealed that 10h and niraparib synergistically enhanced antiproliferative effects against Granta-519. These results suggested that 10h holds promise for further development as a lead compound for the design of ATR kinase-targeted therapies.

Graphical abstract: Discovery of dihydrospiro[cyclopropane-1,7′-pyrrolo[3,4-d]pyrimidine] derivatives as novel ATR inhibitors

Supplementary files

Article information

Article type
Research Article
Submitted
15 Dec 2025
Accepted
17 Feb 2026
First published
16 Mar 2026

RSC Med. Chem., 2026, Advance Article

Discovery of dihydrospiro[cyclopropane-1,7′-pyrrolo[3,4-d]pyrimidine] derivatives as novel ATR inhibitors

X. Chen, Y. Qian, Y. Guo, J. Li, L. Xu, X. Zeng, K. Jiang, Y. Zhou, J. Li and T. Liu, RSC Med. Chem., 2026, Advance Article , DOI: 10.1039/D5MD01127B

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