A reaction mechanism-based prediction of mutagenicity: α-halo carbonyl compounds adduct with DNA by SN2 reaction

Most of the α-halo carbonyl (AHC) compounds tend to be predicted as mutagenic by structure-activity relationship based on structural category only, because they have an alkyl halide structure as a structural alert of mutagenicity. However, some AHC compounds are not mutagenic. We hypothesized that A...

Full description

Saved in:
Bibliographic Details
Published inJournal of toxicological sciences Vol. 43; no. 3; pp. 203 - 211
Main Authors Haranosono, Yu, Ueoka, Hiroki, Kito, Gakushi, Nemoto, Shingo, Kurata, Masaaki, Sakaki, Hideyuki
Format Journal Article
LanguageEnglish
Japanese
Published Suita The Japanese Society of Toxicology 2018
Japan Science and Technology Agency
Subjects
Carbonyl compounds
Carbonyls
Deoxyribonucleic acid
DNA
DNA adducts
Energy gap
Impurities
In silico
Inspection
Molecular orbital
Molecular orbitals
Mutagenicity
Organic chemistry
Predictions
Reaction mechanisms
Reactivity
SN2 reaction
Structure-activity relationships
Visual discrimination
α-Halo carbonyl
Online AccessGet full text

Cover

More Information
Summary:Most of the α-halo carbonyl (AHC) compounds tend to be predicted as mutagenic by structure-activity relationship based on structural category only, because they have an alkyl halide structure as a structural alert of mutagenicity. However, some AHC compounds are not mutagenic. We hypothesized that AHC reacts with DNA by SN2 reaction, and the reactivity relates to mutagenicity. As an index of SN2 reactivity, we focused on molecular orbitals (MOs), as the direction and position of two molecules in collision are important in the SN2 reaction. The MOs suitable for SN2 reaction (SN2MOs) were selected by chemical-visual inspection based on the shape of the MO. We used the level gap and the energy gap between SN2MO and the lowest unoccupied molecular orbital as the descriptors of SN2 reactivity. As the results, SN2 reactivity related to mutagenicity and we were able to predict mutagenicity of 20 AHC compounds with 95.0% concordance. It was suggested that SN2 reaction is a reaction mechanism of AHC compounds and DNA in the mutagenic process. The method allows for discrimination among structurally similar compounds by combination with quantitative structure-activity relationships. The combination approach is expected to be useful for the mutagenic assessment of pharmaceutical impurities.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0388-1350
1880-3989
DOI:10.2131/jts.43.203