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- W4372331965 abstract "Pan-histone deacetylase (HDAC) inhibitors often have some toxic side effects. In this study, three series of novel polysubstituted N-alkyl acridone analogous were designed and synthesised as HDAC isoform-selective inhibitors. Among them, 11b and 11c exhibited selective inhibition of HDAC1, HDAC3, and HDAC10, with IC50 values ranging from 87 nM to 418 nM. However, these compounds showed no inhibitory effect against HDAC6 and HDAC8. Moreover, 11b and 11c displayed potent antiproliferative activity against leukaemia HL-60 cells and colon cancer HCT-116 cells, with IC50 values ranging from 0.56 μM to 4.21 μM. Molecular docking and energy scoring functions further analysed the differences in the binding modes of 11c with HDAC1/6. In vitro anticancer studies revealed that the hit compounds 11b and 11c effectively induced histone H3 acetylation, S-phase cell cycle arrest, and apoptosis in HL-60 cells in a concentration-dependent manner." @default.
- W4372331965 created "2023-05-07" @default.
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- W4372331965 date "2023-05-05" @default.
- W4372331965 modified "2023-09-25" @default.
- W4372331965 title "Discovery of novel polysubstituted <i>N</i>-alkyl acridone analogues as histone deacetylase isoform-selective inhibitors for cancer therapy" @default.
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- W4372331965 doi "https://doi.org/10.1080/14756366.2023.2206581" @default.
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