Mixed‐Model QSAR at the Glucocorticoid Receptor: Predicting the Binding Mode and Affinity of Psychotropic Drugs-Reference-Cited by-同舟云学术

Mixed‐Model QSAR at the Glucocorticoid Receptor: Predicting the Binding Mode and Affinity of Psychotropic Drugs

Published:2009-01-05 Issue:1 Volume:4 Page:100-109
ISSN:1860-7179
Container-title:ChemMedChem
language:en
Short-container-title:ChemMedChem

Author:

Spreafico Morena¹,Ernst Beat¹,Lill Markus A.²,Smiesko Martin¹,Vedani Angelo¹

Affiliation:

1. Department of Pharmaceutical Sciences, University of Basel, Klingelbergstrasse 50, 4056 Basel (Switzerland), Fax: (+41) 61‐267‐1552

2. Department of Medicinal Chemistry and Molecular Pharmacology, Purdue University, West Lafayette, IN 47907 (USA)

Publisher

Wiley

Subject

Organic Chemistry,General Pharmacology, Toxicology and Pharmaceutics,Molecular Medicine,Drug Discovery,Biochemistry,Pharmacology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cmdc.200800274

Reference65 articles.

1. Nuclear-Receptor Ligands and Ligand-Binding Domains

2. T. Damstra S. Barlow A. Bergman R. Kavlock G. Van der Kraak Global Assessment of the State‐of‐the‐Science of Endocrine Disruptors IPCS‐WHO 2002 p. 1.

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