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Prethodno priopćenje
https://doi.org/10.5562/cca2996

Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors

Ante Miličević ; Institute for Medical Research and Occupational Health, Ksaverska c. 2, P.O. Box 291, HR-10001 Zagreb, Croatia
Nenad Raos ; Institute for Medical Research and Occupational Health, Ksaverska c. 2, P.O. Box 291, HR-10001 Zagreb, Croatia

Puni tekst: engleski, pdf (625 KB) str. 511-515 preuzimanja: 761* citiraj
APA 6th Edition
Miličević, A. i Raos, N. (2016). Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors. Croatica Chemica Acta, 89 (4), 511-515. https://doi.org/10.5562/cca2996
MLA 8th Edition
Miličević, Ante i Nenad Raos. "Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors." Croatica Chemica Acta, vol. 89, br. 4, 2016, str. 511-515. https://doi.org/10.5562/cca2996. Citirano 27.09.2021.
Chicago 17th Edition
Miličević, Ante i Nenad Raos. "Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors." Croatica Chemica Acta 89, br. 4 (2016): 511-515. https://doi.org/10.5562/cca2996
Harvard
Miličević, A., i Raos, N. (2016). 'Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors', Croatica Chemica Acta, 89(4), str. 511-515. https://doi.org/10.5562/cca2996
Vancouver
Miličević A, Raos N. Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors. Croatica Chemica Acta [Internet]. 2016 [pristupljeno 27.09.2021.];89(4):511-515. https://doi.org/10.5562/cca2996
IEEE
A. Miličević i N. Raos, "Modelling of Protective Mechanism of Iron(II)-polyphenol Binding with OH-related Molecular Descriptors", Croatica Chemica Acta, vol.89, br. 4, str. 511-515, 2016. [Online]. https://doi.org/10.5562/cca2996

Sažetak
The linear models for the calculation of pIC50, pKa1 and Epa for 12 polyphenolic compounds (catechins, flavonols, catechol and gallol derivatives) were developed. As descriptors we used the number of vicinal (Nv) and non-vicinal (Nnv) OH groups, as well as the number of OH vicinal pairs as possible Fe2+ chelate sites (Nch). The models gave r ˃ 0.9 and standard errors of 0.13, 0.26 and 0.04 for pIC50, pKa1 and Epa, respectively. For modelling of pIC50, Nch is better variable than Nv, and vice versa for modelling of pKa1 and Epa. This result, along with good correlations between pIC50, pKa1 and Epa, suggests two effects for antioxidative activity of polyphenols; their reaction(s) with OH and prevention of Fenton reaction by Fe2+ chelation.

Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 International License.

Ključne riječi
antioxidative activity; Fenton reaction; DNA damage; QSAR

Hrčak ID: 171909

URI
https://hrcak.srce.hr/171909

Posjeta: 1.080 *