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Title: Discovery of novel 4(1H)-quinolone derivatives as potential antiproliferative and apoptosis inducing agents. Author: Zhou P, Huang L, Zhou J, Jiang B, Zhao Y, Deng X, Zhao Q, Li F. Journal: Bioorg Med Chem Lett; 2017 Sep 01; 27(17):4185-4189. PubMed ID: 28757067. Abstract: A series of novel 4(1H)-quinolone derivatives was synthesized and evaluated for antiproliferative activity in vitro. The results showed that these compounds exhibited more potent antiproliferative effect against a panel of human tumorcelllines than the lead compound 7-chloro-4(1H)-quinolone 1. Compound 7e was found to be the most potent antiproliferative agent and to exhibit selective cytotoxic activity against HepG2 cell lines with IC50 value lower than 1.0μM. Annexin V/FITC-PI assay showed that compound 7e induced apoptosis in HepG2 cells with a dose-dependent manner. Western blotting analysis indicated that compound 7e induced cell cycle arrest in G2/M phase by p53-depedent pathway.[Abstract] [Full Text] [Related] [New Search]