Comparison of the QSAR Models for Toxicity and Biodegradability of Anilines and Phenols
Authors
Damborsky, J. and Schultz, T.
Source
CHEMOSPHERE 34: 429-446 (1997)
Abstract
Structure-activity models for toxicity and biodegradability of groups of m-anilines and p-phenols were developed and compared. Hydrophobicity was the most important property in determining toxicity. Whereas, electronic and steric properties were the more important in modeling biodegradation.
