Journal of Molecular Structure p. 488 - 495 (2019)
Update date:2022-08-30
Topics:
Niedzia?kowski, Pawe?
Czaczyk, El?bieta
Jarosz, Joanna
Wcis?o, Anna
Bia?obrzeska, Wioleta
Wietrzyk, Joanna
Ossowski, Tadeusz
The present study describes the synthesis and electrochemical, spectral and biological evaluation of new 9,10-anthraquinone derivatives containing one or two piperidine units incorporated in the different positions of the anthraquinone scaffold. The authors focused their efforts on the characterization of the obtained derivatives using the NMR and IR techniques and on the analysis of the molecules properties using the UV-VIS spectroscopy in the DMSO solution. Additionally, the electrochemical investigation of the compounds was performed using the cyclic voltammetry at the GC (glassy carbon) electrode in the DMSO solution. The primary aim of this study was to determine the antiproliferative activity of the obtained compounds. All novel anthraquinone derivatives containing piperidine unit in the structure were tested in vitro against four human cancer cell lines—HL-60, LoVo, HL-60/MX2, LoVo/Dx—which the latter two are drug-resistant. The tests also included the in vitro analyses of the antiproliferative activities against BALB/3T3 normal mouse fibroblasts cell lines. The results led to an interesting observation concerning the selectivity—all the derivatives exhibit potential anticancer activity against leukemic drug-resistant cell lines. Moreover, the most active compound 1-(piperidin-1-yl)-9,10-anthraquinone 1 inhibited also the proliferation of the colon cancer cell lines, distinctly overcoming the drug-resistance. Its activity towards the cancer cell lines was 5–8 times higher than the activity against normal fibroblasts cell line, which can suggest its selectivity towards cancer cells.
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