Virtual Ligand Screening for Structure-based Drug Design: Approaches and Progress

Recent progress in human genomics and proteomics has significantly increased the number of macromolecular targets potentially involved in drug discovery campaigns. Today technologies like combinatorial chemistry and high-throughput screening (HTS) authorize biological assays of a large number of sma...

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Bibliographic Details
Main Authors: Olivier Sperandio, Maria A. Miteva, Bruno O. Villoutreix
Format: Article
Language:English
Published: Academic Publishing House 2007-10-01
Series:Bioautomation
Subjects:
Online Access:http://www.clbme.bas.bg/bioautomation/2007/vol_7.1/files/7_4.5.pdf