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OverviewBased on the international workshop on 'Small Molecule - Protein Interactions' held in Berlin, April 24-26, 2002, researchers from industry and academic laboratories describe novel and efficient ways selecting promising new drug targets and developing small molecule inhibitors against them. The structure of the book corresponds to the different aspects of the drug discovery process. All chapters are written by leading experts in the field, who present and discuss the most recent state-of-the-art tools and techniques for the development of novel drugs. The value of the book lies in surveying and summarizing the approaches taken by different companies and institutions giving the reader a balanced view on the use of the latest techniques on the one hand and experience-based assistance in selecting appropriate tools for their own work on the other hand. Full Product DetailsAuthor: Herbert Waldmann , Marcus KoppitzPublisher: Springer-Verlag Berlin and Heidelberg GmbH & Co. KG Imprint: Springer-Verlag Berlin and Heidelberg GmbH & Co. K Edition: Softcover reprint of the original 1st ed. 2003 Volume: 42 Dimensions: Width: 14.80cm , Height: 1.30cm , Length: 21.00cm Weight: 0.329kg ISBN: 9783662053164ISBN 10: 3662053160 Pages: 228 Publication Date: 25 December 2012 Audience: Professional and scholarly , Professional & Vocational Format: Paperback Publisher's Status: Active Availability: Manufactured on demand We will order this item for you from a manufactured on demand supplier. Table of Contents1 Drug Discovery Opportunities.- 2 Target Analysis: A Priori Assessment of Druggability.- 3 Drug Discovery at Signaling Interfaces.- 4 Chemical Genomics of Orphan Nuclear Receptors.- 5 High-Throughput X-Ray Techniques and Drug Discovery.- 6 NMR in Medicinal Chemistry.- 7 Creating Knowledge from High-Throughput Screening Data.- 8 From Structure to Recognition Principles: Mining in Crystal Data as a Prerequisite for Drug Design.- 9 Practical Database Screening with Docking Tools.- 10 De Novo Design Methods.- 11 From Protein Domains to Drug Candidates — Natural Products as Guiding Principles in Compound Library Design and Synthesis.- 12 Discovery of New MCRs, Chemical Evolution and Lead Optimization.- 13 The Impact of Combinatorial Chemistry on Drug Discovery.- Previous Volumes Published in This Series.ReviewsAuthor InformationTab Content 6Author Website:Countries AvailableAll regions |
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