A review of the electrophilic reaction chemistry involved in covalent DNA binding
- PMID: 20722585
- DOI: 10.3109/10408444.2010.494175
A review of the electrophilic reaction chemistry involved in covalent DNA binding
Abstract
The need to assess the ability of a chemical to act as a mutagen or a genotoxic carcinogen (collectively termed genotoxicity) is one of the primary requirements in regulatory toxicology. Several pieces of legislation have led to an increased interest in the use of in silico methods, specifically the formation of chemical categories for the assessment of toxicological endpoints. A key step in the development of chemical categories for genotoxicity is defining the organic chemistry associated with the formation of a covalent bond between DNA and an exogenous chemical. This organic chemistry is typically defined as structural alerts. To this end, this article has reviewed the literature defining the structural alerts associated with covalent DNA binding. Importantly, this review article also details the mechanistic organic chemistry associated with each of the structural alerts. This information is extremely important in terms of meeting regulatory requirements for the acceptance of the chemical category approach. The structural alerts and associated mechanistic chemistry have been incorporated into the Organisation for Economic Co-operation and Development (OECD) (Q)SAR Application Toolbox.
Similar articles
-
Development of new structural alerts suitable for chemical category formation for assigning covalent and non-covalent mechanisms relevant to DNA binding.Mutat Res. 2012 Mar 18;743(1-2):10-9. doi: 10.1016/j.mrgentox.2011.12.029. Epub 2012 Jan 12. Mutat Res. 2012. PMID: 22260876
-
A review of the electrophilic reaction chemistry involved in covalent protein binding relevant to toxicity.Crit Rev Toxicol. 2011 Oct;41(9):783-802. doi: 10.3109/10408444.2011.598141. Epub 2011 Aug 2. Crit Rev Toxicol. 2011. PMID: 21809939 Review.
-
Testing computational toxicology models with phytochemicals.Mol Nutr Food Res. 2010 Feb;54(2):186-94. doi: 10.1002/mnfr.200900259. Mol Nutr Food Res. 2010. PMID: 20024931
-
DNA adducts of lactones, sultones, acylating agents and acrylic compounds.IARC Sci Publ. 1994;(125):179-98. IARC Sci Publ. 1994. PMID: 7806312 Review. No abstract available.
-
International Commission for Protection Against Environmental Mutagens and Carcinogens. Approaches to SAR in carcinogenesis and mutagenesis. Prediction of carcinogenicity/mutagenicity using MULTI-CASE.Mutat Res. 1994 Feb 1;305(1):33-46. doi: 10.1016/0027-5107(94)90124-4. Mutat Res. 1994. PMID: 7508546 Review.
Cited by
-
Mouse Models for Immune Checkpoint Blockade Therapeutic Research in Oral Cancer.Int J Mol Sci. 2022 Aug 16;23(16):9195. doi: 10.3390/ijms23169195. Int J Mol Sci. 2022. PMID: 36012461 Free PMC article. Review.
-
Pathways to Identify Electrophiles In Vivo Using Hemoglobin Adducts: Hydroxypropanoic Acid Valine Adduct and Its Possible Precursors.Chem Res Toxicol. 2022 Dec 19;35(12):2227-2240. doi: 10.1021/acs.chemrestox.2c00208. Epub 2022 Nov 17. Chem Res Toxicol. 2022. PMID: 36395356 Free PMC article.
-
Application of in silico and in vitro methods in the development of adverse outcome pathway constructs in wildlife.Philos Trans R Soc Lond B Biol Sci. 2014 Nov 19;369(1656):20130584. doi: 10.1098/rstb.2013.0584. Philos Trans R Soc Lond B Biol Sci. 2014. PMID: 25405971 Free PMC article.
-
QSAR classification of metabolic activation of chemicals into covalently reactive species.Mol Divers. 2012 May;16(2):389-400. doi: 10.1007/s11030-012-9364-3. Epub 2012 Feb 28. Mol Divers. 2012. PMID: 22370994
-
Transitioning to composite bacterial mutagenicity models in ICH M7 (Q)SAR analyses.Regul Toxicol Pharmacol. 2019 Dec;109:104488. doi: 10.1016/j.yrtph.2019.104488. Epub 2019 Oct 3. Regul Toxicol Pharmacol. 2019. PMID: 31586682 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous