5,6-Dimethylchrysene-1,2-Diol-3,4-Epoxide DNA Adducts are Stereoselectively Detected by Antisera Prepared Against the DNA Adducts Formed by the Stereoisomers of Benzo[c]phenanthrene-3,4-Diol-1,2-Epoxide-Reference-Cited by-同舟云学术

5,6-Dimethylchrysene-1,2-Diol-3,4-Epoxide DNA Adducts are Stereoselectively Detected by Antisera Prepared Against the DNA Adducts Formed by the Stereoisomers of Benzo[c]phenanthrene-3,4-Diol-1,2-Epoxide

Published:1994-08 Issue:1-4 Volume:6 Page:63-70
ISSN:1040-6638
Container-title:Polycyclic Aromatic Compounds
language:en
Short-container-title:Polycyclic Aromatic Compounds

Author:

Butch Elizabeth R.,Yagi Haruhiko,Jerina Donald M.,Amin Shantu,Baird William M.

Publisher

Informa UK Limited

Subject

Materials Chemistry,Organic Chemistry,Polymers and Plastics

Link

http://www.tandfonline.com/doi/pdf/10.1080/10406639408031168

Reference16 articles.

1. Polycyclic aromatic hydrocarbons in long-range transported aerosols

2. Jerina, D. M., Sayer, J. M., Agarwal, S. K., Yagi, H., Levin, W., Wood, A. W., Conney, A. H., Pruess-Schwartz, D., Baird, W. M., Pigott, M. A. and Dipple, A. 1986.Biological Reactive Intermediates III, Edited by: Kocsis, J. J., Jollow, D. J., Witmer, C. M., Nelson, J. O. and Snyder, R. 11–30. New York: Plenum.

3. Optically active benzo[c]phenanthrene diol epoxides bind extensively to adenine in DNA

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