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Most drugs bind to a clearly defined macromolecular target that is complementary in terms of structure and chemistry. This observation is the basic paradigm of
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This book provides a complete snapshot of various experimental approaches to structure-based and ligand-based drug design and is illustrated with more than 200
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QSAR and Drug Design: New Developments and Applications
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Based on topics presented at the Annual Japanese (Quantitative) Structure-Activity Relationship Symposium and the Biennial China-Japan Drug Design and Developme