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A high proportion of drugs currently coming to market exert their action in the body by inhibiting a target enzyme involved in a particular body function or in a bacterium, protozoon, or virus causing an infection. This book extends the previous volume in providing a comprehensive coverage of more recently recognized target enzymes and their known inhibitors and, within this framework of knowledge, demonstrates how the drug designer uses all available information to develop a specific therapeutic agent. Drug design is an interdisciplinary art; this text illustrates the pathway followed from the initial design concept and synthesis of an inhibitor, through its in vitro and in vivo assessments, to clinical trial -- a process involving chemists, biochemists, pharmacologists, and clinicians.
This volume investigates the systematic methodology required to design effective therapeutic agents by targeting specific enzymes involved in physiological functions or pathogenic infections. The authors, H. John Smith and Merton Sandler, synthesize interdisciplinary expertise from chemistry, biochemistry, and pharmacology to outline the development pipeline. They provide a framework for translating theoretical design concepts into viable clinical candidates through rigorous assessment protocols.
What You Will Find
Scope Limits
Experts recognize this text as a technical resource for professionals and advanced students involved in medicinal chemistry and drug development. Readers frequently note the high level of academic density and the practical focus on the interdisciplinary nature of pharmaceutical research.
Page Count:
848
Publication Date:
1994-05-26
Publisher:
Oxford University Press
ISBN-10:
0192621343
ISBN-13:
9780192621344
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