Quantitative structure-activity relationships (QSARs) for skin corrosivity of organic acids, bases and phenols: Principal components and neural network analysis of extended datasets
- 1 February 1996
- journal article
- Published by Elsevier in Toxicology in Vitro
- Vol. 10 (1) , 85-94
- https://doi.org/10.1016/0887-2333(95)00101-8
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- The use of in vitro cytotoxicity measurements in QSAR methods for the prediction of the skin corrosivity potential of acidsToxicology in Vitro, 1996
- A quantitative structure-activity relationship for the eye irritation potential of neutral organic chemicalsToxicology Letters, 1995
- Practical applications of QSAR to in vitro toxicology illustrated by consideration of eye irritationToxicology in Vitro, 1995
- Quantitative structure-activity relationships for skin permeabilityToxicology in Vitro, 1995
- Quantitative structure activity relationships for skin corrosivity of organic acids, bases and phenolsToxicology Letters, 1995
- The identification and classification of skin irritation hazard by a human patch testFood and Chemical Toxicology, 1994
- Development of an automatic estimation system for both the partition coefficient and aqueous solubilityJournal of Computer-Aided Molecular Design, 1991
- Automatic log P estimation based on combined additive modeling methodsJournal of Computer-Aided Molecular Design, 1990
- Interspecies comparisons of skin irritancyToxicology and Applied Pharmacology, 1975