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• W4310118433 abstract "Abstract Centriole duplication occurs once per cell cycle and is regulated by Polo‐like kinase 4 (PLK4). Overexpression of PLK4 in somatic cells can lead to the excessive formation of centrioles, directly causing chromosome segregation errors and tumorigenesis. In this study, we described our efforts to develop a series of PLK4 inhibitors with 1 H ‐pyrazolo[3,4‐ d ]pyrimidine core, and further structure‐ and receptor‐based design and optimization resulted in a potent inhibitor WY29 (IC 50 = 0.027 μM), which exhibited good selectivity to other PLK family members (PLK1‐3). At the cellular level, compound WY29 showed excellent antiproliferative activity against three breast cancer cell lines (MCF‐7, BT474, and MDA‐MB‐231) while weak inhibitory activity was found on normal cell line HUVECs. In addition, the in vitro preliminary drug‐like properties evaluation of compound WY29 showed outstanding stability in human plasma and liver microsomes, and weak inhibitory activity against the major subtypes of human cytochrome P450. Also, the drug‐like properties prediction of compound WY29 displayed remarkable drug‐like properties (drug‐likeness mode score: 1.06). In conclusion, these results support the further development of compound WY29 as a lead compound for PLK4‐targeted anticancer drug discovery." @default.
• W4310118433 created "2022-11-30" @default.
• W4310118433 creator A5007126456 @default.
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• W4310118433 date "2022-11-28" @default.
• W4310118433 modified "2023-10-14" @default.
• W4310118433 title "Design, synthesis, and biological evaluation of a potent PLK4 inhibitor WY29 with 1<i>H</i>‐pyrazolo[3,4‐<i>d</i>]pyrimidine scaffold" @default.
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• W4310118433 doi "https://doi.org/10.1002/ardp.202200490" @default.
• W4310118433 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/36442843" @default.
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