Chlorine substitution promotes phenyl radical loss from C8-phenoxy-2′-deoxyguanosine adducts: implications for biomarker identification from chlorophenol exposure-Reference-Cited by-同舟云学术

Chlorine substitution promotes phenyl radical loss from C8-phenoxy-2′-deoxyguanosine adducts: implications for biomarker identification from chlorophenol exposure

Published:2015-01 Issue:1 Volume:50 Page:81-87
ISSN:1076-5174
Container-title:Journal of Mass Spectrometry
language:en
Short-container-title:J. Mass Spectrom.

Author:

Witham Aaron A.¹,Sharma Purshotam²,Wetmore Stacey D.²,Gabryelski Wojciech¹,Manderville Richard A.¹

Affiliation:

1. Department of Chemistry and Toxicology; University of Guelph; Guelph ON N1G 2W1 Canada

2. Department of Chemistry and Biochemistry; University of Lethbridge; Lethbridge AB T1K 3M4 Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Publisher

Wiley

Subject

Spectroscopy

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/jms.3475/fullpdf

Reference38 articles.

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3. DNA Damage by Phenoxyl Radicals

4. Quinoids, quinoid radicals, and phenoxyl radicals formed from estrogens and antiestrogens;Bolton;Toxicology,2002

5. Role of quinones in toxicology;Bolton;Chem. Res. Toxicol.,2000

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