Modern methods of drug discovery

By:

Hillisch, Alexander

Contributor(s):

Hilgenfeld, Rolf

Language: ENG Publication details: Basel Springer 2009Edition: 1stDescription: 292, 23.5*15.8 Pages | Binding - Paperback |ISBN:

978-81-8489-150-8

Subject(s):

PHARMACEUTICAL CHEMISTRY

DDC classification:

615.19 HIL DDC23

Online resources:

Click here to access online

Summary: This volume offers a broad and interdisciplinary view of modern approaches to drug discovery as used by pharmaceutical companies and research institutes. It comprehensively covers proteomics, bioinformatics, screening techniques such as high-throughput-, natural compounds-, and NMR-based-screenings, combinatorial chemistry, compound library design, ligand- and structure-based drug design and pharmacokinetic approaches. Each of the thirteen chapters reviews the theory, background and application of a key technology in drug discovery, complemented by an extensive list of references to the original literature. This concise source of information will be useful for researchers, both in industry and academia, as well as students in the fields of medicinal, pharmaceutical and computational chemistry, bioinformatics, biochemistry, molecular biology and pharmacology.

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Holdings
Item type	Current library	Collection	Call number	Status	Barcode
Books	School of Pharmacy Reference Section	Reference	615.19 HIL (Browse shelf(Opens below))	Not For Loan	B2870
Books	School of Pharmacy General Stacks	Reference	615.19 HIL (Browse shelf(Opens below))	Available	B0807

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Previous	615.19 GRI Textbook of pharmaceutical medicine	615.19 GRI Introduction to medicinal chemistry	615.19 HAR Pharmaceutical process chemistry for synthesis	615.19 HIL Modern methods of drug discovery	615.19 JEN/KNE Quantitative pharmaceutical chemistry	615.19 JHO/LEA Structure based drug discovery	615.19 KAD/MAH Principles of medicinal chemistry	Next

This volume offers a broad and interdisciplinary view of modern approaches to drug discovery as used by pharmaceutical companies and research institutes. It comprehensively covers proteomics, bioinformatics, screening techniques such as high-throughput-, natural compounds-, and NMR-based-screenings, combinatorial chemistry, compound library design, ligand- and structure-based drug design and pharmacokinetic approaches. Each of the thirteen chapters reviews the theory, background and application of a key technology in drug discovery, complemented by an extensive list of references to the original literature. This concise source of information will be useful for researchers, both in industry and academia, as well as students in the fields of medicinal, pharmaceutical and computational chemistry, bioinformatics, biochemistry, molecular biology and pharmacology.

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