275375-54-7Relevant academic research and scientific papers
Microwave-assisted multistep synthesis of functionalized 4-arylquinolin-2(1H)-ones using palladium-catalyzed cross-coupling chemistry
Glasnov, Toma N.,Stadlbauer, Wolfgang,Kappe, C. Oliver
, p. 3864 - 3870 (2007/10/03)
Biologically active 4-aryl-3-alkenyl-substituted quinolin-2(1H)-ones have been synthesized in a short and concise manner employing readily available 4-hydroxyquinolin-2(1H)-ones as intermediates. Key steps in the synthesis include the derivatization of th
4-Aryl-3-(hydroxyalkyl)quinolin-2-ones: Novel maxi-K channel opening relaxants of corporal smooth muscle targeted for erectile dysfunction
Hewawasam, Piyasena,Fan, Wenhong,Ding, Min,Flint, Kim,Cook, Deborah,Goggins, Gregory D.,Myers, Robert A.,Gribkoff, Valentin K.,Boissard, Christopher G.,Dworetzky, Steven I.,Starrett Jr., John E.,Lodge, Nicholas J.
, p. 2819 - 2822 (2007/10/03)
Novel 4-aryl-3-(hydroxyalkyl)quinoline-2-one derivatives were prepared and evaluated as openers of the cloned maxi-K channel hSlo expressed in Xenopus laevis oocytes by utilizing electrophysiological methods. The effect of these maxi-K openers on corporal
3-SUBSTITUTED-4-ARYLQUINOLIN-2-ONE DERIVATIVES AS POTASSIUM CHANNEL MODULATORS
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, (2008/06/13)
The present invention provides novel 3-substituted-4-arylquinolin-2-one derivatives having the general formula wherein R, R 1, R 2, R 3, R 4, R 5, R 6 and R 7 are as defined herein, or a non-toxic pharmaceutically acceptable salt thereof which are modulators of the large conductance calcium-activated K + channels and are useful in the treatment of disorders which are responsive to the opening of the potassium channels.
