Computational Investigation into the Oxidation of Guanine to Form Imidazolone (Iz) and Related Degradation Products
Author:
Affiliation:
1. Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States
Funder
Division of Chemistry
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.chemrestox.0c00039
Reference72 articles.
1. How Easily Oxidizable Is DNA? One-Electron Reduction Potentials of Adenosine and Guanosine Radicals in Aqueous Solution
2. Mechanisms of Formation, Genotoxicity, and Mutation of Guanine Oxidation Products
3. Guanine Oxidation: One- and Two-Electron Reactions
4. Formation and processing of DNA damage substrates for the hNEIL enzymes
5. Formation of 8-oxo-7,8-dihydroguanine-radicals in -irradiated DNA by multiple one-electron oxidations
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1. Theoretical insights into the reaction mechanism of hydroxyl radicals and guanine in G-quadruplex DNA;Physical Chemistry Chemical Physics;2023
2. An Exploration of the Transformation of the 8‐Oxo‐7,8‐Dihydroguanine Radical Cation to Protonated 2‐Amino‐5‐Hydroxy‐7,9‐Dihydropurine‐6,8‐Dione in a Base Pair;ChemPhysChem;2022-10-27
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4. Synthesis, In Silico Prediction and In Vitro Evaluation of Antimicrobial Activity, DFT Calculation and Theoretical Investigation of Novel Xanthines and Uracil Containing Imidazolone Derivatives;International Journal of Molecular Sciences;2021-10-12
5. Design, Synthesis, and Antimicrobial Activity of Novel Fluorine-Containing Imidazolones;Russian Journal of Organic Chemistry;2021-06
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