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Chem Biol Interact ; 212: 40-6, 2014 Apr 05.
Article in English | MEDLINE | ID: mdl-24508591

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-ß-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.


Subject(s)
Flavanones/chemistry , Flavanones/pharmacology , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , Oximes/chemistry , Animals , Cell Line, Tumor , Cell Proliferation , Chemistry Techniques, Synthetic , Dogs , Drug Evaluation, Preclinical , Flavanones/chemical synthesis , Free Radical Scavengers/chemical synthesis , Hydrogen Peroxide/chemistry , Hydroxyl Radical/chemistry , Superoxides/chemistry
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