Synthesis, Characterization, and Comparative 32P-Postlabeling Efficiencies of 2,6-Dimethylaniline−DNA Adducts-Reference-Cited by-同舟云学术

Synthesis, Characterization, and Comparative 32P-Postlabeling Efficiencies of 2,6-Dimethylaniline−DNA Adducts

Published:2001-01-05 Issue:2 Volume:14 Page:165-174
ISSN:0893-228X
Container-title:Chemical Research in Toxicology
language:en
Short-container-title:Chem. Res. Toxicol.

Author:

Gonçalves Luísa L.¹,Beland Frederick A.¹,Marques M. Matilde¹

Affiliation:

1. Centro de Química Estrutural, Complexo I, Instituto Superior Técnico, Av. Rovisco Pais, 1049-001 Lisboa, Portugal, and Division of Biochemical Toxicology, National Center for Toxicological Research, Jefferson, Arkansas 72079

Publisher

American Chemical Society (ACS)

Subject

Toxicology,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/tx0002031

Reference47 articles.

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2. Chemical Studies on Tobacco Smoke LXIV. On the Analysis of Aromatic Amines in Cigarette Smoke*

3. U.S. National Toxicology Program (1990) Toxicology and carcinogenesis studies of 2,6-xylidine (2,6-dimethylaniline) (CAS No. 87-62-7) in Charles River CD rats (feed studies), Technical Report Series No. 278, National Toxicology Program, Research Triangle Park, NC.

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