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Pharmacokinetics and Metabolism in Drug Design (Methods and Principles in Medicinal Chemistry)
 
 
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Pharmacokinetics and Metabolism in Drug Design (Methods and Principles in Medicinal Chemistry) [Hardcover]

Dennis A. Smith (Author), Han Waterbeemd (Author), Don K. Walker (Author), Raimund Mannhold (Series Editor), Hugo Kubinyi (Series Editor), Gerd Folkers (Series Editor)

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Book Description

3527313680 978-3527313686 May 2, 2006 2
In this new edition of a bestseller, all the contents have been updated and new material has been added, especially in the areas of toxicity testing and high throughput analysis. The authors, all of them employed at Pfizer in the discovery and development of new active substances, discuss the significant parameters and processes important for the absorption, distribution and retention of drug compounds in the body, plus the potential problems created by their transformation into toxic byproducts. They cover everything from the fundamental principles right up to the impact of pharmacokinetic parameters on the discovery of new drugs.

While aimed at all those dealing professionally with the development and application of pharmaceutical substances, the readily comprehensible style makes this book equally suitable for students of pharmacy and related subjects.


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Editorial Reviews

Review

"This work will interest and inform both the beginning professional in the field of drug discovery/design and the medicinal chemist…I also highly recommend it for students…" (Journal of Medicinal Chemistry, December 14, 2006)

"…extremely useful to students of Toxicology and others with an interest in the subject." (British Toxicology Society Newsletter, Summer 2007)

From the Back Cover

An understanding of pharmacokinetics is necessary to ensure that drugs that are active in vitro will also be active in the human body. The optimization of the pharmacokinetic properties of lead compounds is therefore of central importance to drug development.

In this new edition of a bestseller, all the contents have been updated and new material has been added, especially in the areas of toxicity testing and high throughput analysis. The authors, all of them employed at Pfizer in the discovery and development of new active substances, discuss the significant parameters and processes important for the absorption, distribution and retention of drug compounds in the body, plus the potential problems created by their transformation into toxic byproducts. They cover everything from the fundamental principles right up to the impact of pharmacokinetic parameters on the discovery of new drugs.

From the contents:
  • Physicochemistry
  • Pharmacokinetics
  • Absorption
  • Distribution
  • Clearance
  • Renal Clearance
  • Metabolic (Hepatic) Clearance
  • Toxicity
  • Inter-Species Scaling
  • High(er) Throughput ADME Studies

While aimed at all those dealing professionally with the development and application of pharmaceutical substances, the clear and accessible style makes this book equally suitable for teaching students of pharmacy and related subjects, especially for those who feel that pharmacokinetics is covered too briefly in the standard textbooks.


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Inside This Book (learn more)
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First Sentence:
The body can be viewed as primarily composed of a series of membrane barriers dividing aqueous filled compartments. Read the first page
Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
daily dose size, intrinsic lipophilicity, unbound renal clearance, slow offset, unbound clearance, human clearance, intrinsic clearance, total drug concentrations, direct equilibrium, catalytic selectivity, allometric exponent, unbound drug, tissue affinity, neutral drugs, increasing lipophilicity, drug clearance, hepatic extraction, systemic clearance, allometric relationship, membrane transfer, thiophene ring, allometric scaling, paracellular route, absorption potential, basic drugs
Key Phrases - Capitalized Phrases (CAPs): (learn more)
Van de Waterbeemd, Drug Metab, New York, Activity Relat, Drug Discov, Drug Research, Eds Testa, Pharmacokinetic Optimization, Plenum Press, Drug Dispos, Eds Borchardt, Eds Pliska, Raevsky H-bond
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