EVALUATION OF ANTIOXIDANT ACTIVITY OF SOME IMINES DERIVATIVES OF L-ARGININE

Authors

  • Andreea-Teodora IACOB University of Medicine and Pharmacy “Grigore T. Popa”- Iasi
  • Maria DRAGAN University of Medicine and Pharmacy “Grigore T. Popa”- Iasi
  • Sandra CONSTANTIN University of Medicine and Pharmacy “Grigore T. Popa”- Iasi
  • Florentina LUPASCU University of Medicine and Pharmacy “Grigore T. Popa”- Iasi
  • Luminita CONFEDERAT University of Medicine and Pharmacy “Grigore T. Popa”- Iasi
  • F. BURON University of Orléans - Orléans, France
  • S. ROUTIER University of Orléans - Orléans, France
  • Lenuta PROFIRE University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

Keywords:

L-ARGININE, IMINE, ANTIOXIDANT ACTIVITY

Abstract

L-Arginine is an α-amino acid which plays important roles in different diseases or processes, such as Alzheimer disease, inflammatory process, healing and tissue regeneration and it also could be useful as an anti-atherosclerotic agent. Aim: Considering the large amount of studies on the beneficial effects of different antioxidants, this paper is focused on the evaluation of the antioxidant potential of some imine derivatives, synthesized by the authors and described in a previous article. Material and Methods: The evaluation of the antioxidant power was performed using phosphomolydenum-reducing antioxidant power (PRAP) and ferric reducing antioxidant power (FRAP) assays, tests described in the literature and which are used with some minor modifications. Results: It was found that most of the imine derivatives are more active than the L-Arginine in the PPAP and FRAP assays. The most active derivative was the compound obtained by condensation of L-arginine with 2,3-dihydroxybenzaldehyde (2k) and 2-nitrobenzaldehyde (2g). Conclusions: Following the described protocol, some imine derivatives of L-arginine were evaluated in terms of antioxidant potential using in vitro methods. The most favorable influence was obtained by the aromatic substitution with nitro and hydroxyl, the corresponding derivatives being the most active derivatives compared to L-arginine.

Author Biographies

  • Andreea-Teodora IACOB, University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

    Faculty of Pharmacy
    Department of Pharmaceutical Chemistry

  • Maria DRAGAN, University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

    Faculty of Pharmacy
    Department of Pharmaceutical Chemistry

  • Sandra CONSTANTIN, University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

    Faculty of Pharmacy
    Department of Pharmaceutical Chemistry

  • Florentina LUPASCU, University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

    Faculty of Pharmacy
    Department of Pharmaceutical Chemistry

  • Luminita CONFEDERAT, University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

    Faculty of Pharmacy
    Department of Pharmaceutical Chemistry

  • F. BURON, University of Orléans - Orléans, France

    Institute of Organic and Analytical Chemistry

  • S. ROUTIER, University of Orléans - Orléans, France

    Institute of Organic and Analytical Chemistry

  • Lenuta PROFIRE, University of Medicine and Pharmacy “Grigore T. Popa”- Iasi

    Faculty of Pharmacy
    Department of Pharmaceutical Chemistry

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Additional Files

Published

2016-06-30