Abstract
The realization of pharmacological effects of nitroxyl radicals, i.e., their antitumor, radiosensitizing, anti-aggregating, and possibly, neuropsychotropic activity, appears to be largely determined by the free radical nitroxyl moiety [1]. Nitroxyls are known to be effective traps for reactive radicals, especially, for the radicals which are formed during oxidation of the organic compounds [2, 3]. Similar to their precursors, sterically hindered nitrous heterocycles, they prove to be effective antioxidants [2].
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Abbreviations
- L:
-
lipids of biomembrane
- L.; LO.; LOO. :
-
lipid radicals
- \( O_{2}^{\underline{.}} \) :
-
superoxide anion
- CBA:
-
breaking of the LPO chain by Ä“-acceptor antioxidant
- CBD:
-
breaking of the LPO chain by Ä“-donoe antioxidant
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Komarov, P.G., Morgunov, A.A., Bilenko, M.V., Zhdanov, R.I. (1992). Anti-Ischemic Effect of 1-Hydroxy Derivatives of Nitroxyl Bioantioxidants. In: Zhdanov, R.I. (eds) Bioactive Spin Labels. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-48724-8_20
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