Pregled bibliografske jedinice broj: 947404
Evaluation of antiproliferative effect of 2, 6, 7-trihydroxy-9-phenyl-3H-xanthene-3-one derivates in vitro
Evaluation of antiproliferative effect of 2, 6, 7-trihydroxy-9-phenyl-3H-xanthene-3-one derivates in vitro // 12th Central European Oncology Congress, Croatian Society of Oncology’s Best of ASCO® Conference ; 22-25.06.2015
Opatija, Hrvatska, 2015. (poster, međunarodna recenzija, neobjavljeni rad, znanstveni)
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Naslov
Evaluation of antiproliferative effect of 2, 6, 7-trihydroxy-9-phenyl-3H-xanthene-3-one derivates in vitro
Autori
Harej, Anja ; Klobučar, Marko ; Kraljević Pavelić, Sandra
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, neobjavljeni rad, znanstveni
Izvornik
12th Central European Oncology Congress, Croatian Society of Oncology’s Best of ASCO® Conference ; 22-25.06.2015
/ - , 2015
Skup
12th Central European Oncology Congress, Croatian Society of Oncology’s Best of ASCO® Conference ; 22-25.06.2015
Mjesto i datum
Opatija, Hrvatska, 22.06.2015. - 25.06.2015
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
xanthen-3-one derivatives, antiproliferative evaluation, antioxidant potency
Sažetak
Ten biologically active xanthen-3-one derivatives were synthesized. Structures of novel compounds were confirmed by IR, 1H, 13C NMR and mass spectrometry. Majority of tested compounds exerted antiproliferative effects at higher tested concentrations (10–100 µM). Compound 9-(4-chlorophenyl)-2, 6, 7-trihydroxyxanthen-3-one (4) exerted the most potent and selective antiproliferative activity in the micromolar range (0.1–10 µM) on all tested cell lines except on SW620 and is thus suitable for further biological evaluation. The strongest effect of compound 4 on HeLa cells was accompained by induction of mitotic catastrophe and apoptotis. Some of the synthesized compounds were scanned for their antioxidant potency using electrochemical method cyclic voltammetry of immobilized microparticles. Electrochemical behaviour of studied compounds was compared to the basic non-substituted compound. Shift of the biological oxidation potential towards lower values was obtained for the substituted compounds pointing to the improvement in the reducing power of the compounds.
Izvorni jezik
Engleski
POVEZANOST RADA