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.

Full text

Citation

Damborsky, J. and Schultz, T., 1997: Comparison of the QSAR Models for Toxicity and Biodegradability of Anilines and Phenols. Chemosphere 34: 429-446.

Gaspar a Gaussian Expert
1st Hands-on Computational Enzyme Design Workshop
Marie Curie Fellowship for Dmitri
Rayyan Announced as Best Presenter
Researchers’ Night 2019 in LL
Open Postdoctoral Position: Protein Structural Biologist
Andrea Awarded for Excellent Research