Abstract
Ligand-based drug design represents an important research field in the drug discovery and optimisation process. This review provides an overview about the theoretical background of the quantitative structure activity relationship (QSAR) models.
Keywords: Ligand-based drug design, chemometrics, quantitative structure-activity relationship (QSAR), drug discovery
Current Drug Discovery Technologies
Title: Ligand-Based Drug Design Methodologies in Drug Discovery Process: An Overview
Volume: 3 Issue: 3
Author(s): Magdalena Bacilieri and Stefano Moro
Affiliation:
Keywords: Ligand-based drug design, chemometrics, quantitative structure-activity relationship (QSAR), drug discovery
Abstract: Ligand-based drug design represents an important research field in the drug discovery and optimisation process. This review provides an overview about the theoretical background of the quantitative structure activity relationship (QSAR) models.
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Cite this article as:
Bacilieri Magdalena and Moro Stefano, Ligand-Based Drug Design Methodologies in Drug Discovery Process: An Overview, Current Drug Discovery Technologies 2006; 3 (3) . https://dx.doi.org/10.2174/157016306780136781
DOI https://dx.doi.org/10.2174/157016306780136781 |
Print ISSN 1570-1638 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6220 |
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