Please use this identifier to cite or link to this item: https://idr.l1.nitk.ac.in/jspui/handle/123456789/13314
Title: Synthesis, chemical characterization of novel 1,3-dimethyl acridones as cytotoxic agents, and their DNA-binding studies
Authors: Sathish, N.K.
GopKumar, P.
Rajendra, Prasad, V.V.S.
Shanta, Kumar, S.M.
Mayur, Y.C.
Issue Date: 2010
Citation: Medicinal Chemistry Research, 2010, Vol.19, 7, pp.674-689
Abstract: A series of new 1,3-dimethyl acridone derivatives were synthesized with different alkyl side chain (propyl and butyl) substitution at N 10-position and highly basic amine groups at terminal end of alkyl side chain. All the synthesized molecules were screened for their cytotoxic activity against human breast adenocarcinoma (MCF-7) and human promyelocytic leukemia (HL-60) cell lines. DNA binding constants (Ki) of selected compounds were determined with calf-thymus DNA. Results showed that the molecules 7, 8, 10, 11, 12, 13, 14, and 15 exhibited good cytotoxic activity with IC50 value <10 ?M. Compound 14 having (?- hydroxyethyl) piperazine butyl side chain exhibited potent cytotoxic activity against MCF-7 cell line and DNA-intercalating properties. Examination of the relationship between lipophilicity and acridone derivatives showed poor correlation. Birkh user Boston 2009.
URI: http://idr.nitk.ac.in/jspui/handle/123456789/13314
Appears in Collections:1. Journal Articles

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