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• W2000299703 abstract "In search of new selective anti-cancer agents, a series of sixteen novel 2-aminoimidazole–quinoline hybrid compounds ( 5a – 5p ) have been designed and synthesized regioselectively. We have characterized the compounds extensively using IR, 1D and 2D NMR Spectroscopy and mass spectrometry. The cytotoxicity studies against different cancer cell lines showed that the compound 5a (Imd–Ph) emerged as a potent cytotoxic scaffold. Imd–Ph ( 5a ) exhibited a selective anticancer activity against human colon cancer cell line (HCT-116, DLD-1) and was found relatively non-toxic to breast cancer cells (MDA-MB-231) as well as to normal primary endothelial cells (HUVEC). Structure–activity relationship of imidazole–quinoline hybrid scaffolds revealed differential and selective toxicities exerted by the different derivatives against cancer and normal cells. Structural modification of the scaffold with library of a wide variety of substituents may lead to the development of novel selective anti-cancer agents in the future. • Sixteen 2-aminoimidazole–quinoline hybrid compounds synthesized regioselectively. • The structure with E -configuration was established on the basis of 2D NMR. • Imidazole–quinoline hybrid (Imd–Ph) is a potent scaffold for anticancer drug discovery. • Imd–Ph scaffold is relatively non-toxic to normal primary endothelial cells (HUVEC)." @default.
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• W2000299703 date "2014-11-01" @default.
• W2000299703 modified "2023-10-16" @default.
• W2000299703 title "Design, regioselective synthesis and cytotoxic evaluation of 2-aminoimidazole–quinoline hybrids against cancer and primary endothelial cells" @default.
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• W2000299703 doi "https://doi.org/10.1016/j.ejmech.2014.09.055" @default.
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