Waiting
Login processing...

Trial ends in Request Full Access Tell Your Colleague About Jove
JoVE Journal
Bioengineering

This content is Open Access.

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors
 
Click here for the English version

In Silico Modeling Method for Computational Aquatic Toxicology of Endocrine Disruptors: A Software-Based Approach Using QSAR Toolbox

Article DOI: 10.3791/60054-v 05:47 min August 28th, 2019
August 28th, 2019

Chapters

Summary

Please note that all translations are automatically generated.

Click here for the English version.

Die quantitative Struktur-Aktivitäts-Beziehungsmodellierung (QSAR) ist eine repräsentative bioinformatische Methode im toxikologischen Screening. Dieses Protokoll zeigt, wie die Risiken von endokrinen Disruptoren (EDs) in aquatischen Umgebungen rechnerisch bewertet werden. Mit Hilfe der OECD QSAR Toolbox implementiert das Protokoll einen in silico assay zur Analyse der Toxizität von EDs bei Fischen.

Tags

Bioengineering Ausgabe 150 OECD QSAR Toolbox automatisierter Workflow quantitative Struktur-Aktivitäts-Beziehung QSAR endokrine Störende chemikarine aquatische Wirbeltiere akute Toxizität computational ecotoxicology
Read Article

PLAYLIST

Pharmaceutical Chemistry Formulation of introductory drug. Generic and Ethical Drugs Pre-formulation: Introduction, influencing factors
Active SAR Functional Groups (Pharmacopoeial Colloids: Difference between Colloidal Solutions, Colloid Types) Stability Emulsions: Types of Emulsions (Selection of HLB Composition and Properties, Milk Calculations The quantitative relationship between the drug's structure and its activity (QSAR) (types of surfactants, composition and properties, stability enhancement methods, substances) - Drug Design Strategies 8 Optimize interactions with the target site
Opiate painkillers (nsaids) nonsteroidal anti-bacterial (antibacterial drugs) Need for controlled release drugs: Defined release versus controlled release, drug controlled release types, diffusion-based systems and transdermal systems Design and Synthesis of Drugs Microcapsulation Peptides for Drugs: Microcapsules
Preparation of tablets by the wet granulation method and the examination of the physicochemical properties of the tablets

Get cutting-edge science videos from JoVE sent straight to your inbox every month.

Waiting X
Simple Hit Counter