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DC Field | Value | Language |
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dc.contributor.author | Sathish, N.K. | - |
dc.contributor.author | GopKumar, P. | - |
dc.contributor.author | Rajendra, Prasad, V.V.S. | - |
dc.contributor.author | Shanta, Kumar, S.M. | - |
dc.contributor.author | Mayur, Y.C. | - |
dc.date.accessioned | 2020-03-31T08:45:35Z | - |
dc.date.available | 2020-03-31T08:45:35Z | - |
dc.date.issued | 2010 | - |
dc.identifier.citation | Medicinal Chemistry Research, 2010, Vol.19, 7, pp.674-689 | en_US |
dc.identifier.uri | http://idr.nitk.ac.in/jspui/handle/123456789/13314 | - |
dc.description.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. | en_US |
dc.title | Synthesis, chemical characterization of novel 1,3-dimethyl acridones as cytotoxic agents, and their DNA-binding studies | en_US |
dc.type | Article | en_US |
Appears in Collections: | 1. Journal Articles |
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