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Produktbild: Structure-Based Drug Discovery
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Produktbild: Structure-Based Drug Discovery

Structure-Based Drug Discovery

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Structure-based drug discovery methods have been transformed in the last 5-10 years and are now having a major impact on the discovery of new drugs. Some of the most exciting developments in the field, such as Fragment-based methods, are described in this book.

The book describes the latest developments in technologies that can be used to obtain the 3-D structures including the high profile structural genomics approaches being utilised worldwide. The use of 3-D protein structures in new, Fragment-based, approaches to drug discovery are described in some detail. This book includes experimental approaches using X-ray crystallography and NMR for Fragment-based screening as well as other biophysical methods for studying protein/ligand interactions. In addition, developments in computational chemistry methodology are covered together with an assessment of practical applications.

Inhaltsverzeichnis

Five Years of Increasing Structural Biology Throughput - A Retrospective Analysis. - Protein Production for Structural Genomics - Strategies for the Next Phase. - to Fragment Screening. - Fragment-Based NMR Screening in Lead Discovery. - Fragment-Based Screening by X-ray Crystallography. - Scaffold-Based Drug Discovery. - Biophysical Methods. - Illustration of Current Challenges in Molecular Docking. - Scoring Functions.

Produktdetails

Erscheinungsdatum
09. Januar 2007
Sprache
englisch
Auflage
2007 edition
Seitenanzahl
250
Herausgegeben von
Harren Jhoti, Andrew R Leach
Illustrationen
XII, 250 p.
Verlag/Hersteller
Produktart
gebunden
Abbildungen
XII, 250 p.
Gewicht
522 g
Größe (L/B/H)
244/163/23 mm
ISBN
9781402044069

Pressestimmen

From the reviews:



" Structure-based drug design (SBDD) is now an integral component of the drug discovery process. The book s core subject matter of fragment-based screening is an exciting and important development in drug discovery. These chapters are generally the strongest in the book and make it a good reference volume . " (Robert Powers, Journal of the American Chemical Society, Vol. 129 (32), 2007)

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