A Reevaluation of the Ambident Reactivity of the Guanine Moiety Towards Hydroxyl Radicals-Reference-Cited by-同舟云学术

A Reevaluation of the Ambident Reactivity of the Guanine Moiety Towards Hydroxyl Radicals

Published:2009-03-09 Issue:12 Volume:48 Page:2214-2217
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Chatgilialoglu Chryssostomos,D'Angelantonio Mila,Guerra Maurizio,Kaloudis Panagiotis,Mulazzani Quinto G.

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference36 articles.

1. Structure and acid-base properties of one-electron-oxidized deoxyguanosine, guanosine, and 1-methylguanosine

2. Ionization of purine nucleosides and nucleotides and their components by 193-nm laser photolysis in aqueous solution: model studies for oxidative damage of DNA

3. Oxidation of Guanine by Carbonate Radicals Derived from Photolysis of Carbonatotetramminecobalt(III) Complexes and the pH Dependence of Intrastrand DNA Cross-Links Mediated by Guanine Radical Reactions

4. The reduction potential of one-electron oxidized guanosine, E7(2/1)) 1.29 V,[4] is lower than that of SO4.−, Br2.−, CO3.−, and HO. radicals,[5] which means that in principle these species can oxidize guanosine or 2-deoxyguanosine by one-electron transfer.

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