The lock-and-key principle formulated by Emil Fischer as early as the end of the 19th century has still not lost any of its significance for the life sciences. The basic aspects of ligand-protein interaction may be summarized under the term 'molecular recognition' and concern the specificity as well as stability of ligand binding. Molecular recognition is thus a central topic in the development of active substances, since stability and specificity determine whether a substance can be used as a drug. Nowadays, computer-aided prediction and intelligent molecular design make a large contribution to the constant search for, e. g., improved enzyme inhibitors, and new concepts such as that of pharmacophores are being developed. An up-to-date presentation of an eternally young topic, this book is an indispensable information source for chemists, biochemists and pharmacologists dealing with the binding of ligands to proteins.

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знания и навыки

Protein-Ligand Interactions

Animal Models for Human Cancer. Discovery and Development of Novel Therapeutics

Fragment-based Drug Discovery. Lessons and Outlook

Pharmacokinetics and Metabolism in Drug Design

In vivo Models for Drug Discovery

Reactive Drug Metabolites

Scaffold Hopping in Medicinal Chemistry

Data Mining in Drug Discovery

Drug Metabolism Prediction

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Hugo Kubinyi Protein-Ligand Interactions

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