Synthesis of Oligonucleotides and Thermal Stability of Duplexes Containing the β-C-Nucleoside Analogue of Fapy·dG
Author:
Affiliation:
1. Department of Chemistry, Johns Hopkins University, Baltimore, Maryland 21218, and Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/tx025588x
Reference33 articles.
1. Chemistry of Glycosylases and Endonucleases Involved in Base-Excision Repair
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1. Synthesis of Oligonucleotides Containing the N 6 ‐(2‐Deoxy‐α,β‐ d ‐erythropentofuranosyl)‐2,6‐diamino‐4‐hydroxy‐5‐formamidopyrimidine (Fapy⋅dG) Oxidative Damage Product Derived from 2′‐Deoxyguanosine;Chemistry – A European Journal;2020-04-09
2. Aminolysis of 6-[1-(2,6-difluorophenyl)cyclopropyl]-5-methyl-2-(nitroamino)pyrimidin-4(3H)-one;Russian Journal of Organic Chemistry;2017-12
3. C(2)-Functionalization of pyrimidin-4(3H)-one derivatives in the synthesis of its biologically active derivatives;Russian Chemical Bulletin;2015-11
4. Solution Structure of Duplex DNA Containing a β-Carba-Fapy-dG Lesion;Chemical Research in Toxicology;2012-08-29
5. The Formamidopyrimidines: Purine Lesions Formed in Competition With 8-Oxopurines From Oxidative Stress;Accounts of Chemical Research;2011-11-11
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