83707-37-3Relevant academic research and scientific papers
Synthesis and evaluation of N-Benzyl-acridinone derivatives induced apoptosis in human liver cancer cell-lines
Huang, Xian-Feng,Yulan-Zhua,Zhu, Hai-Liang
, p. 606 - 611 (2011)
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.
Alkylation en catalyse par transfert de phase d'une serie d'acridanone-9 substituees: Competition entre O- et N-alkylation
Mahamoud, Abdallah,Galy, Jean-Pierre,Vincent, Emile-Jean,Galy, Anne-Marie,Barbe, Jacques
, p. 503 - 507 (2007/10/02)
Substituted acridanones were alkylated under phase transfer catalysis conditions.In so doing, a mixture of O- and N-alkyl derivatives was prepared.Orientation of the reaction products depends upon the alkylating agent but not on the position of the substi
