Related Experiment Video
Updated: Mar 27, 2026

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox
Published on: August 28, 2019
Investigating the mechanisms of bioconcentration through QSAR classification trees
Francesca Grisoni1, Viviana Consonni1, Marco Vighi2
1University of Milano-Bicocca, Dept. of Earth and Environmental Sciences, Milano, Italy; Milano Chemometrics and QSAR Research Group, Milano, Italy.
Abstract:
This paper proposes a scheme to predict whether a compound (1) is mainly stored within lipid tissues, (2) has additional storage sites (e.g., proteins), or (3) is metabolized/eliminated with a reduced bioconcentration. The approach is based on two validated QSAR (Quantitative Structure-Activity Relationship) trees, whose salient features are: (a) descriptor interpretability and (b) simplicity. Trees were developed for 779 organic compounds, the TGD approach was used to quantify the lipid-driven bioconcentration, and a refined machine-learning optimization procedure was applied. We focused on molecular descriptor interpretation, which allowed us to gather new mechanistic insights into the bioconcentration mechanisms.
More Related Videos
10:29Quantitative Structure-Activity Relationship, Activity Prediction, and Molecular Dynamics of Non-nucleotide Reverse Transcriptase Inhibitors
Published on: May 9, 2025
03:29Author Spotlight: Advancing Therapeutics to Treat Vibriosis in Humans and Aquatic Organisms
Published on: May 31, 2024
Related Concept Videos
Structure-Activity Relationships and Drug Design
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence...
Mechanistic Models: Compartment Models in Individual and Population Analysis
Bioavailability Enhancement: Determination and Conceptual Approaches in Overcoming Bioavailability Problems
Quantitative Aspects of Drug-Receptor Interaction
Mechanistic Models: Overview of Compartment Models
Pharmacodynamic Models: Linear Concentration–Effect Model