. "55" . "5"^^ . . "D\u017Eub\u00E1k, Petr" . "RIV/61989592:15110/14:33151900!RIV15-MSM-15110___" . . . "[7AF91DE1E7BE]" . "26" . . . . "3"^^ . "Motyka, Kamil" . "Tetrahedron Letters" . "http://www.sciencedirect.com/science/article/pii/S0040403914007588" . . . "10.1016/j.tetlet.2014.04.121" . . "Hajd\u00FAch, Mari\u00E1n" . "49018" . . . "Kadri\u010D, Jasna" . . "Synthesis, cytotoxic activity and fluorescence properties of a set of novel 3-hydroxyquinolin-4(1H)-ones" . "Solid-phase synthesis, hydroxyquinolinones, cytotoxic activity, fluorescence"@en . "P(ED0030/01/01), P(EE2.3.20.0009), P(EE2.4.31.0130)" . "Soural, Miroslav" . "Synthesis, cytotoxic activity and fluorescence properties of a set of novel 3-hydroxyquinolin-4(1H)-ones" . "000337868300004" . . . . "Synthesis, cytotoxic activity and fluorescence properties of a set of novel 3-hydroxyquinolin-4(1H)-ones"@en . "RIV/61989592:15110/14:33151900" . "4"^^ . "15110" . "The targeted solid-phase synthesis of 3-hydroxyquinolin-4(1H)-one derivatives is described. The primary and secondary amines, 3-amino-4-(methoxycarbonyl)benzoic acid and 2-bromo-1-(4-chloro-3-nitrophenyl)ethanone were used as starting materials. The structures of the final compounds were designed in accordance with previous information obtained from structure-activity relationship studies of similar cytotoxic derivatives. Representative prepared compounds were subjected to in vitro screening of cytotoxic activity against various cancer cell lines; the results obtained are discussed. Fluorescence properties of selected compounds were also studied to compare the data with those obtained in analogous derivatives." . . . "0040-4039" . "Synthesis, cytotoxic activity and fluorescence properties of a set of novel 3-hydroxyquinolin-4(1H)-ones"@en . . . "GB - Spojen\u00E9 kr\u00E1lovstv\u00ED Velk\u00E9 Brit\u00E1nie a Severn\u00EDho Irska" . "The targeted solid-phase synthesis of 3-hydroxyquinolin-4(1H)-one derivatives is described. The primary and secondary amines, 3-amino-4-(methoxycarbonyl)benzoic acid and 2-bromo-1-(4-chloro-3-nitrophenyl)ethanone were used as starting materials. The structures of the final compounds were designed in accordance with previous information obtained from structure-activity relationship studies of similar cytotoxic derivatives. Representative prepared compounds were subjected to in vitro screening of cytotoxic activity against various cancer cell lines; the results obtained are discussed. Fluorescence properties of selected compounds were also studied to compare the data with those obtained in analogous derivatives."@en .