| Literature DB >> 24508591 |
Mustafa Ozyürek1, Damla Akpınar2, Mustafa Bener2, Baki Türkkan3, Kubilay Güçlü2, Reşat Apak2.
Abstract
Recent interest in polyphenolic antioxidants due to their involvement in health benefits has led to the investigation of new polyphenolic compounds with enhanced antioxidant activity. Naringin (4',5,7-trihydroxyflavanone-7-β-l-rhamnoglucoside-(1,2)-α-d-glucopyranoside) is one of the major flavanones in citrus and grapefruit. The present study aimed to synthesize naringin oxime from naringin and to evaluate its antioxidant and anticancer potential using in vitro assay system. The structure of the synthesized compound, naringin oxime, was elucidated by FT-IR, (1)H NMR, elemental analysis and UV-vis spectroscopy. Antioxidant capacity of naringin oxime, as measured by the cupric reducing antioxidant capacity (CUPRAC) method, was found to be higher than that of the parent compound naringin. Other parameters of antioxidant activity (scavenging effects on OH, O2(-), and H2O2) of naringin and naringin oxime were also determined.Entities:
Keywords: Antioxidant activity; Cupric reducing antioxidant capacity (CUPRAC) assay; Flavanone oximes; Naringin; Naringin oxime
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Year: 2014 PMID: 24508591 DOI: 10.1016/j.cbi.2014.01.017
Source DB: PubMed Journal: Chem Biol Interact ISSN: 0009-2797 Impact factor: 5.192