Literature DB >> 24508591

Novel oxime based flavanone, naringin-oxime: synthesis, characterization and screening for antioxidant activity.

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.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Antioxidant activity; Cupric reducing antioxidant capacity (CUPRAC) assay; Flavanone oximes; Naringin; Naringin oxime

Mesh:

Substances:

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


  7 in total

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Authors:  Joanna Kozłowska; Bartłomiej Potaniec; Barbara Żarowska; Mirosław Anioł
Journal:  Molecules       Date:  2017-09-06       Impact factor: 4.411

5.  A Systematic Review of the Preventive and Therapeutic Effects of Naringin Against Human Malignancies.

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Journal:  Front Pharmacol       Date:  2021-03-29       Impact factor: 5.810

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Journal:  Molecules       Date:  2021-11-17       Impact factor: 4.411

7.  Naringin protects myocardial cells from doxorubicin‑induced apoptosis partially by inhibiting the p38MAPK pathway.

Authors:  Chun-Yan Jian; Han-Bin Ouyang; Xian-Hong Xiang; Jia-Li Chen; Yong-Xin Li; Xin Zhou; Jin-Yang Wang; Yang Yang; En-Yi Zhong; Wen-Hua Huang; Hong-Wu Zhang
Journal:  Mol Med Rep       Date:  2017-10-19       Impact factor: 2.952

  7 in total

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