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Antiradical activity of the hormonal preparation estrone in lipid models undergoing oxidation

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Abstract

The rate constants and stoichiometric coefficients of chain termination in the oxidation of lipid models (methyl esters of acids of the oleic series: cis-6-, cis-9-, trans-9-, and trans-11-C17H33COOCH3) by the main representative of the follicular hormones — estrone (313–348 K) — and for comparison by the phenol 2,6-ditert-butyl-4-methylphenol (323.15 K) were measured. The strength of the OH bond in the estrone molecule was estimated.

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Authors and Affiliations

  1. Institute of Bioorganic Chemistry and Petrochemistry, Academy of Sciences of the Ukraine, Kiev

    G. A. Kovtun & V. A. Pluzhnikov

Authors
  1. G. A. Kovtun
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  2. V. A. Pluzhnikov
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Translated from Teoreticheskaya i Éksperimental'naya Khimiya, Vol. 29, No. 5, pp. 445–448, September–October, 1993.

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Kovtun, G.A., Pluzhnikov, V.A. Antiradical activity of the hormonal preparation estrone in lipid models undergoing oxidation. Theor Exp Chem 29, 297–299 (1994). https://doi.org/10.1007/BF00531466

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  • DOI: https://doi.org/10.1007/BF00531466

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