Abstract
The synthesis and spectroscopic characterization of trans 1-(indol-2-yl)-2-(1-methylpyridinium and 1-methylquinolinium-2-yl) ethylenes is reported. In vitro antitumour activity tests show that quinolinium derivatives are more active towards MCF7 (breast), LNCap (prostate) and U87 (human gliobastoma) carcinoma cells than pyridinium ones.
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APA
Fortuna, C. G., Barresi, V., Musso, N., & Musumarra, G. (2009). Synthesis and applications of new trans 1-indolyl-2-(1-methyl pyridinium and quinolinium-2-yl)ethylenes. Arkivoc, 2009(8), 222–229. https://doi.org/10.3998/ark.5550190.0010.819
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