Synthesis and Evaluation of N-Benzyl-Acridinone Derivatives Induced Apoptosis in Human Liver Cancer Cell-Lines

Title: Synthesis and Evaluation of N-Benzyl-Acridinone Derivatives Induced Apoptosis in Human Liver Cancer Cell-Lines

Volume: 8 Issue: 7

Author(s): Xian-Feng Huang, Yulan-Zhu and Hai-Liang Zhu

Affiliation:

Keywords: Acridinone, Antiproliferative activity, Apoptosis, HepG2 cell, N-benzyl-acridinone, antiproliferative, agarose gel electrophoresis, cytotoxicity, Annexin V-FITC/PI staining assay, chemotherapeutic agents, Hepatocellular carcinoma (HCC), metastasis, hydrophobic, Jourdan, –, Ulmann copper-catalysed condensation

Abstract: A series of N-benzyl-9(10H)-acridinones were synthesized and tested for their antitumor activities in vitro against HepG2 cells.Assay-based antiproliferative activity study using HepG2 cell lines revealed that several compounds had significant effects on cytotoxicity, among which compound 5h was found to be the most active compound with IC50 at about 1.33 μM using the MTT assay. The antitumor effect of compound 5h is believed to be due to the induction of apoptosis, which was further confirmed by Hoechst 33258 fluorescence staining, agarose gel electrophoresis and Annexin VFITC/ PI staining assay using flow cytometry analysis. Above all, compound 5h would be a potential anticancer agent which deserves further research.

Cite this article as:

Huang Xian-Feng, Yulan-Zhu and Zhu Hai-Liang, Synthesis and Evaluation of N-Benzyl-Acridinone Derivatives Induced Apoptosis in Human Liver Cancer Cell-Lines, Letters in Drug Design & Discovery 2011; 8 (7) . https://dx.doi.org/10.2174/157018011796235176

DOI https://dx.doi.org/10.2174/157018011796235176	Print ISSN 1570-1808
Publisher Name Bentham Science Publisher	Online ISSN 1875-628X