143084-41-7Relevant academic research and scientific papers
Fluorescent properties and conformational preferences of C-linked phenolic-DNA adducts
Omumi, Alireza,Millen, Andrea L.,Wetmore, Stacey D.,Manderville, Richard A.
, p. 1694 - 1709 (2011)
Phenolic toxins and mutagenic diazoquinones generate C-linked adducts at the C8 site of 2′-deoxyguanosine (dG) through the intermediacy of radical species. We have previously reported the site-specific incorporation of these adducts into oligonucleotides
Concerning the hydrolytic stability of 8-aryl-2′-deoxyguanosine nucleoside adducts: Implications for abasic site formation at physiological pH
Schlitt, Katherine M.,Sun, Ke-Wen M.,Paugh, Robert J.,Millen, Andrea L.,Navarro-Whyte, Lex,Wetmore, Stacey D.,Manderville, Richard A.
experimental part, p. 5793 - 5802 (2009/12/26)
(Chemical Equation Presented) Direct addition of aryl radical species to the C8-site of 2′-deoxyguanosine (dG) affords C 8-aryl-dG adducts that are produced by carcinogenic arylhydrazines, polycyclic aromatic hydrocarbons (PAHs), and
