143084-40-6Relevant articles and documents
Biomarkers for phenol carcinogen exposure act as pH-sensing fluorescent probes
Sun, Kewen M.,McLaughlin, Christopher K.,Lantero, Dean R.,Manderville, Richard A.
, p. 1894 - 1895 (2007)
Biomarkers for phenolic carcinogen exposure, 8-(4″)-hydroxyphenyl)-2′-deoxypurines, have been found to possess pH-sensitive fluorescent properties. Phenolic ionization constants (pKa) establish substituent (σ-) constants of 0.46 for
Fluorescent properties and conformational preferences of C-linked phenolic-DNA adducts
Omumi, Alireza,Millen, Andrea L.,Wetmore, Stacey D.,Manderville, Richard A.
experimental part, p. 1694 - 1709 (2012/04/23)
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
Oxidation of a biomarker for phenol carcinogen exposure: Expanding the redox chemistry of 2 -deoxyguanosine
Weishar, Jennifer L.,McLaughlin, Christopher K.,Baker, Michael,Gabryelski, Wojciech,Manderville, Richard A.
supporting information; experimental part, p. 1839 - 1842 (2009/04/10)
A biomarker for phenolic carcinogen exposure, 8-(4 -hydroxyphenyl)-2 -deoxyguanosine, has been found to undergo oxidative coupling in the presence of Na2lrCl6 to afford ortho-ortho C-C-coupled polyphenols through the Intermedlacy of
