Antiradical activity of delphinidin, pelargonidin and malvin towards hydroxyl and nitric oxide radicals: The energy requirements calculations as a prediction of the possible antiradical mechanisms
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Conformational analysis of delphinidin, pelargonidin and malvin was performed.

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<img border="0" alt="radical dot" data-inlimg="/entities/rad" src="/sd/grey_pxl.gif" class="glyphImg imgLazyJSB">OH and <img border="0" alt="radical dot" data-inlimg="/entities/rad" src="/sd/grey_pxl.gif" class="glyphImg imgLazyJSB">NO antiradical activity was examined theoretically and experimentally.

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EPR measurements proved Dp, Pg and Mv was selective towards hydroxyl radical.

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EPR measurements proved Dp, Pg and Mv was not selective towards nitric oxide.

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Molecules investigated reacted with hydroxyl radical via HAT and SPLET mechanisms.

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