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The Impact of Stereochemistry on Drug Development and Use [Hardcover]

Hassan Y. Aboul-Enein (Author), Irving W. Wainer (Author)

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Book Description

March 28, 1997 0471596442 978-0471596448 1
Provides an authoritative source of practical information on stereochemistry and its impact on drug development. Unlike other books which focus on synthesis, this work explores analytical, pharmacological, and regulatory topics in dealing with the theory and practice of stereochemistry in the pharmaceutical industry today. It specifically addresses how the body metabolizes chiral molecules; the varying effects of different chiral molecules; and provides detailed evaluations of current seperation techniques. Includes regulatory information.

Editorial Reviews

From the Publisher

Provides an authoritative source of practical information on stereochemistry and its impact on drug development. Unlike other books which focus on synthesis, this work explores analytical, pharmacological, and regulatory topics in dealing with the theory and practice of stereochemistry in the pharmaceutical industry today. It specifically addresses how the body metabolizes chiral molecules; the varying effects of different chiral molecules; and provides detailed evaluations of current seperation techniques. Includes regulatory information.

From the Inside Flap

The past fifteen years have seen a revolution in the field of stereochemistry, with breakthrough analytical techniques in enantiomeric separation profoundly affecting drug development and use. This practical reference written by leading researchers focuses on the important roles chirality and stereoisomerism play in drug development efforts-presenting for the first time a comprehensive overview of this rapidly evolving area of pharmacological research. The book explores analytical, pharmacological, and regulatory topics in dealing with the theory and practice of stereochemistry in the pharmaceutical industry today. This exciting, broad-appeal treatment extends from the analytical viewpoint in enantiomeric separation to the regulatory issues involved in the "racemate-versus-enantiomer" debate. The authors include numerous examples and case studies, and integrate material from a wide range of studies, publications, and workshops. The introductory chapters outline the pharmacological effects of stereochemistry, cover stereochemistry in drug metabolism, and discuss problems inherent in the duality of enantiomers-chemically identical yet spatially different molecules. Contributions on the specific aspects of chirality and drug activity explore the toxicological effects of stereoselectivity, illustrate how an understanding of the stereochemical composition of certain drugs can help avoid problems, and offer tips on new clinical applications for existing drugs. A full chapter is devoted to research opportunities in the development of new chirally pure drugs. Other practical research topics range from the preparation of chirally pure compounds to the analytical determination of stereochemical composition, to applications of circular dichroism (CD) spectroscopy. Regulatory issues concerning the development and approval of stereoisomeric drugs are discussed in the final chapters. This section offers an international perspective as well as a historical review of the ongoing debate surrounding regulatory guidelines. The Impact of Stereochemistry on Drug Development and Use is an essential reference for medicinal and analytical chemists, pharmacologists, drug metabolism and pharmacokinetic scientists, and personnel of regulatory agencies. It is also a useful text for graduate students in stereochemistry, and for anyone who wants to keep up with the swift pace of change in this dynamic field.

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Inside This Book (learn more)
First Sentence:
Symmetry or asymmetry is one of the interesting features of geometric figures with two of more dimensions. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
tranylcypromine enantiomers, beclobric acid, carvedilol enantiomers, microsomal epoxide hydrolase catalyzed hydrolysis, carprofen glucuronides, hexobarbital enantiomers, chiral drug substance, aglycone levels, flunoxaprofen enantiomers, chiral barbiturates, oxirane carbon atom, carboxylic acid drugs, chiral selector concentration, talinolol enantiomers, product enantioselectivity, acyl glucuronide formation, chiral discrimination mechanism, pentobarbital enantiomers, labile glucuronides, synthetic chiral surfactants, selected enantiomer, carboxylic acid enantiomers, substrate enantioselectivity, chiral resolving power, stereoisomeric drugs
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Drug Metab, New York, John Wiley, Chemical Analysis Series, Marcel Dekker, United States, The Impact of Stereochemistry, Tetrahedron Asym, European Union, High Res, Naunyn Schmiedeberg's Arch, Johann Wolfgang Goethe-University, Academic Press, Agents Chemother, Department of Pharmacy, Tetrahedron Lett, Pharmaceutical Sciences, Department of Pharmacology, Life Sci, Cancer Res, Drug Dispos, European Community, International Symposium, Lederle Laboratories, Plenum Press
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