Drug Design [[electronic resource] ] : Methodology, Concepts, and Mode-of-Action / / by Gerhard Klebe

• Autore: Klebe Gerhard
• Pubblicazione: Berlin, Heidelberg : , : Springer Berlin Heidelberg : , : Imprint : Springer, , 2013
• Edizione: 1st ed. 2013.
• Descrizione fisica: 1 online resource (496 illus., 333 illus. in color. eReference.)
• Disciplina: 610
• Soggetto topico: Medicine; Pharmacology; Pharmaceutical technology; Medicinal chemistry; Pharmacy; Biomedicine, general; Pharmacology/Toxicology; Pharmaceutical Sciences/Technology; Medicinal Chemistry; Medicine/Public Health, general
• Note generali: Bibliographic Level Mode of Issuance: Monograph
• Nota di contenuto: Part I Fundamentals in Drug Research -- 1. Drug Research Yesterday, Today and Tomorrow -- 2. The Role of Serendipity in Drug Research -- 3. Classical Drug Research -- 4. Protein–Ligand Interactions as the Basis for Drug Action -- 5. Optical Activity and Biological Effects -- Part II Discovery and Optimization of Lead Compounds -- 6. Screening for Lead Structures -- 7. Screening Technologies for Lead Discovery -- 8. Optimization of Lead Structures -- 9. Designing prodrugs -- 10. Peptidomimetics -- Part III Experimental and Theoretical Methods -- 11. Combinatorics: Chemistry With Big Numbers -- 12. Gene Technology in drug research -- 13. Experimental Methods of Structure Determination -- 14. The Spatial Structure of Biomolecules -- 15. Molecular Modelling -- 16. Conformational Analysis -- Part IV Structure–Activity Relationships and Design Approaches -- 17.Pharmacophore Hypothesis and Molecular Comparisons -- 18. Quantitative Structure–Activity Relationships -- 19. From in vitro to in vivo: Optimization of ADME-Tox Properties -- 20. Protein Modeling and Structure-Based Drug Design -- 21. A Case Study: Structure-Based Inhibtor Design for tRNA-Guanine Transglycosylase -- Part V. Drugs and drug action: Successes of structure-based design -- 22. How drugs act: Concepts for therapy -- 23. Inhibitors of hydrolases With an acyl-enzyme intermediate -- 24. Asparticprotease inhibitors -- 25. Inhibitors of hydrolysing metalloenzymes -- 26. Inhibitors of transferases -- 27. Inhibitors of oxidoreductases -- 28. Agonists and antagonists of nuclear receptors -- 29. Agonists and antagonists of membrane-bound -- 30. Ligands for channels, pores and transporters -- 31. Ligands for surface receptors -- 32. Biologicals: Peptides, proteins, nucleotides and macrolides as drugs.
• Sommario/riassunto: Unique work on structure-based drug design, covering multiple aspects of drug discovery and development. Fully colored, many images, computer animations of 3D structures (these only in electronic form). Makes the spatial aspects of interacting molecules clear to the reader, covers multiple applications and methods in drug design. Structures by mode of action, no therapeutic areas. Of high relevance for academia and industrial research. Focus on gene technology in drug design, omics-technologies computational methods experimental techniques of structure determination multiple examples on mode of action of current drugs, ADME-tox properties in drug development, QSAR methods, combinatorial chemistry, biologicals, ribosome, targeting protein-protein interfaces.
• Titolo autorizzato: Drug Design
• ISBN: 3-642-17907-X
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910437839503321
• Lo trovi qui: Univ. Federico II