Design, synthesis, and biological evaluation of a potent PLK4 inhibitor WY29 with 1H‐pyrazolo[3,4‐d]pyrimidine scaffold

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 1H‐pyrazolo[3,4‐d]pyrimidine core, and further structure‐ and receptor‐based design and optimization resulted in a potent inhibitor WY29 (IC50 = 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.

Design, synthesis, and biological evaluation of novel pyrimidin-2-amine derivatives as potent PLK4 inhibitors

“…Subsequently, combined with previous work, we learned that the hydrophobic cavity next to the DFG motif has a significant impact on PLK4 inhibitor activity. 33,34 Given that the complex substituent on the centrinone right side cannot be well embedded in the hydrophobic cavity, we expected to replace this group with an appropriate aromatic ring to reach the hydrophobic cavity. Compounds 3a–3d were synthesized firstly.…”