| Literature DB >> 24096067 |
Bartłomiej Potaniec1, Małgorzata Grabarczyk, Monika Stompor, Antoni Szumny, Paweł Zieliński, Anna Katarzyna Żołnierczyk, Mirosław Anioł.
Abstract
Oximes of isoxanthohumol (IXN), naringenin (N) and flavanone (FL) were synthesized with yields of 88-95% and their antioxidant activity was evaluated using the 1,1-diphenyl-2-picrylhydrazyl radical (DPPH) method. Although naringenin oxime (NOX) and flavanone oxime (FLOX) did not have any significant antioxidant effect (EC50=2.21 mM and 78.7 mM, respectively), isoxanthohumol oxime (IXNOX) showed a strong antioxidant activity (EC50=0.0411 mM), comparable to the activity of ascorbic acid (EC50=0.0181 mM). The structure of new compound IXNOX was established using (1)H NMR, (13)C NMR, IR and UV-VIS spectroscopy, by comparison to IXN, NOX and FLOX.Entities:
Keywords: Antioxidant activity; DPPH method; Isoxanthohumol oxime; NMR–IR–UV spectra; Synergism
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Year: 2013 PMID: 24096067 DOI: 10.1016/j.saa.2013.09.018
Source DB: PubMed Journal: Spectrochim Acta A Mol Biomol Spectrosc ISSN: 1386-1425 Impact factor: 4.098