Carboxymethylnaringenin: a promising antioxidant in the aqueous physiological environment

The synthetic naringenin derivative (2S)-8-carboxymethylnaringenin (<b>CMN</b>) was developed for the treatment of bacterial and viral respiratory infections. There are indications that <b>CMN</b> may act as an antioxidant, however, no studies have been conducted in this regard. This work is aimed at assessing the antiradical capacity of <b>CMN</b> against various physiologically relevant species in physiological environments by using thermodynamic and kinetic calculations. According to the results, <b>CMN</b> only exhibits modest HOO<sup>•</sup> antiradical activity in lipid medium, modeled here as pentyl ethanoate solvent, with an overall rate constant (<i>k</i><sub>overall</sub>) of 2.01 × 10<sup>2</sup> M<sup>−1</sup> s<sup>−1</sup>. However, significant antiradical activity is predicted for the aqueous medium (<i>k</i><sub>overall</sub> = 2.60 × 10<sup>5</sup> M<sup>−1</sup>s<sup>−1</sup>) that is equivalent to the activity of the reference antioxidant Trolox. In a screen performed on a range of radicals, HO<sup>•</sup>, NO<sub>2</sub>, SO<sub>4</sub><sup>•−</sup>, N<sub>3</sub><sup>•</sup>, CH<sub>3</sub>O<sup>•</sup>, CCl<sub>3</sub>O<sup>•</sup>, CH<sub>3</sub>OO<sup>•,</sup> and CCl<sub>3</sub>OO<sup>•</sup> were also successfully scavenged by <b>CMN</b> in water at physiological pH. Therefore, other than a potent drug, <b>CMN</b> is also a good antioxidant in polar environments.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28417695.v1
Primary Topic
Free Radicals and Antioxidants
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article
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Carboxymethylnaringenin: a promising antioxidant in the aqueous physiological environment

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Free Radicals and Antioxidants
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Carboxymethylnaringenin: a promising antioxidant in the aqueous physiological environment

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Abstract

The synthetic naringenin derivative (2S)-8-carboxymethylnaringenin (<b>CMN</b>) was developed for the treatment of bacterial and viral respiratory infections. There are indications that <b>CMN</b> may act as an antioxidant, however, no studies have been conducted in this regard. This work is aimed at assessing the antiradical capacity of <b>CMN</b> against various physiologically relevant species in physiological environments by using thermodynamic and kinetic calculations. According to the results, <b>CMN</b> only exhibits modest HOO<sup>•</sup> antiradical activity in lipid medium, modeled here as pentyl ethanoate solvent, with an overall rate constant (<i>k</i><sub>overall</sub>) of 2.01 × 10<sup>2</sup> M<sup>−1</sup> s<sup>−1</sup>. However, significant antiradical activity is predicted for the aqueous medium (<i>k</i><sub>overall</sub> = 2.60 × 10<sup>5</sup> M<sup>−1</sup>s<sup>−1</sup>) that is equivalent to the activity of the reference antioxidant Trolox. In a screen performed on a range of radicals, HO<sup>•</sup>, NO<sub>2</sub>, SO<sub>4</sub><sup>•−</sup>, N<sub>3</sub><sup>•</sup>, CH<sub>3</sub>O<sup>•</sup>, CCl<sub>3</sub>O<sup>•</sup>, CH<sub>3</sub>OO<sup>•,</sup> and CCl<sub>3</sub>OO<sup>•</sup> were also successfully scavenged by <b>CMN</b> in water at physiological pH. Therefore, other than a potent drug, <b>CMN</b> is also a good antioxidant in polar environments.

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Free Radicals and Antioxidants
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