SAR Models for Metabolic Activation: Stability of Organic Cation Intermediates
- 1 January 1995
- journal article
- research article
- Published by Wiley in Quantitative Structure-Activity Relationships
- Vol. 14 (3) , 264-269
- https://doi.org/10.1002/qsar.19950140306
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Modeling cyanide release from nitriles: prediction of cytochrome P 450-mediated acute nitrile toxicityChemical Research in Toxicology, 1992
- Stabilities of hydrocarbons and carbocations. 1. A comparison of augmented 6-31G, 6-311G, and correlation consistent basis setsJournal of the American Chemical Society, 1992
- Molecular mechanisms of quinone cytotoxicityChemico-Biological Interactions, 1991
- The OASIS concept for predicting the biological activity of chemical compoundsJournal of Mathematical Chemistry, 1990
- Redox cycling of radical anion metabolites of toxic chemicals and drugs and the Marcus theory of electron transfer.Environmental Health Perspectives, 1990
- Redox Cycling of Radical Anion Metabolites of Toxic Chemicals and Drugs and the Marcus Theory of Electron TransferEnvironmental Health Perspectives, 1990
- Predictive models for photoinduced acute toxicity of polycyclic aromatic hydrocarbons to Daphnia magna, strauss (cladocera, crustacea)Environmental Toxicology and Chemistry, 1987
- Quantitative correlation studies between the acute lethal toxicity of 15 organic halides to the guppy (Poecillah Reticulata) and chemical reactivity towards 4‐nitrobenzylpyridineToxicological & Environmental Chemistry, 1985
- Theoretical study on the alkylation and protonation of the nucleic acid basesJournal of Theoretical Biology, 1984
- Application of the Principle of Hard and Soft Acids and Bases to Organic ChemistryJournal of the American Chemical Society, 1967