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• W2806283324 abstract "Abstract WEE1 kinase regulates the G 2 /M cell‐cycle checkpoint, a critical mechanism for DNA repair in cancer cells that can confer resistance to DNA‐damaging agents. We previously reported a series of pyrazolopyrimidinones based on AZD1775, a known WEE1 inhibitor, as an initial investigation into the structural requirements for WEE1 inhibition. Our lead inhibitor demonstrated WEE1 inhibition in the same nanomolar range as AZD1775, and potentiated the effects of cisplatin in medulloblastoma cells, but had reduced single‐agent cytotoxicity. These results prompted the development of a more comprehensive series of WEE1 inhibitors. Herein we report a series of pyrazolopyrimidinones and identify a more potent WEE1 inhibitor than AZD1775 and additional compounds that demonstrate that WEE1 inhibition can be achieved with reduced single‐agent cytotoxicity. These studies support that WEE1 inhibition can be uncoupled from the potent cytotoxic effects observed with AZD1775, and this may have important ramifications in the clinical setting where WEE1 inhibitors are used as chemosensitizers for DNA‐targeted chemotherapy." @default.
• W2806283324 created "2018-06-13" @default.
• W2806283324 creator A5043083588 @default.
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• W2806283324 date "2018-07-11" @default.
• W2806283324 modified "2023-09-26" @default.
• W2806283324 title "Development of Potent Pyrazolopyrimidinone-Based WEE1 Inhibitors with Limited Single-Agent Cytotoxicity for Cancer Therapy" @default.
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• W2806283324 doi "https://doi.org/10.1002/cmdc.201800188" @default.
• W2806283324 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6370589" @default.
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• W2806283324 hasPublicationYear "2018" @default.
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