Synthesis and 32P-Postlabeling/High-Performance Liquid Chromatography Separation of Diastereomeric 1,N2-(1,3-Propano)-2‘-deoxyguanosine 3‘-Phosphate Adducts Formed from 4-Hydroxy-2-nonenal-Reference-Cited by-同舟云学术

Synthesis and 32P-Postlabeling/High-Performance Liquid Chromatography Separation of Diastereomeric 1,N2-(1,3-Propano)-2‘-deoxyguanosine 3‘-Phosphate Adducts Formed from 4-Hydroxy-2-nonenal

Published:1997-11-01 Issue:11 Volume:10 Page:1259-1265
ISSN:0893-228X
Container-title:Chemical Research in Toxicology
language:en
Short-container-title:Chem. Res. Toxicol.

Author:

Yi Ping¹,Zhan DeJin¹,Samokyszyn Victor M.¹,Doerge Daniel R.¹,Fu Peter P.¹

Affiliation:

1. National Center for Toxicological Research, Jefferson, Arkansas 72079, and Department of Pharmacology, University of Arkansas for Medical Sciences, Little Rock, Arkansas 72205

Publisher

American Chemical Society (ACS)

Subject

Toxicology,General Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/tx970100r

Reference44 articles.

1. Chen, H.J. C., and Chung, F.L. (1996) Epoxidation oftrans-4-hydroxy-2-nonenal by fatty acid hydroperoxides and hydrogen peroxide.Chem. Res. Toxicol.9, 306−312.

2. Sodum, R. S., and Chung, F.L. (1988) 1,N2-Ethenodeoxyguanosine as a potential marker for DNA adduct formation bytrans-4-hydroxy-2-nonenal.Cancer Res.48, 320−323.

3. Structural characterization of adducts formed in the reaction of 2,3-epoxy-4-hydroxynonanal with deoxyguanosine

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