Structure-antioxidant activity relationships, QSAR, DFT calculation, and mechanisms of flavones and flavonols
Author:
Publisher
Springer Science and Business Media LLC
Subject
Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics
Link
http://link.springer.com/content/pdf/10.1007/s00044-019-02452-z.pdf
Reference37 articles.
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2. Ali HM, Ali IH (2017) A DFT and QSAR study of the role of 3-, 5-, 7- and 4’-hydroxyl groups in charge and unpaired-electron resonance of anthocyanidins and their radicals. Med Chem Res 26:2666–2674. https://doi.org/10.1007/s00044-017-1964-0
3. Ali HM, Ali IH (2018) Energetic and electronic computation of the two-hydrogen atom donation process in catecholic and non-catecholic anthocyanidins. Food Chem 243:145–150. https://doi.org/10.1016/j.foodchem.2017.09.120
4. Amić D, Davidović -Amić D, Beṧlo D, Trinajstić N (2003) Structure-radical scavenging activity relationships of flavonoids. Croatica Chem Acta 76:55–61
5. Aparicio S (2010) A systematic computational study on flavonoids. Int J Mol Sci 11:2017–2038
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