<p>Although parallel synthesis combined with high-throughput screening has made it easier to generate highly potent drug candidates, many of these compounds never make the grade because they either prove to be unsafe or lack the necessary physicochemical and pharmacokinetic properties. In Optimizati
Optimization in Drug Discovery: In Vitro Methods
β Scribed by Gary W. Caldwell, Becki Hasting, John A. Masucci (auth.), Gary W. Caldwell, Zhengyin Yan (eds.)
- Publisher
- Humana Press
- Year
- 2014
- Tongue
- English
- Leaves
- 596
- Series
- Methods in Pharmacology and Toxicology
- Edition
- 2
- Category
- Library
No coin nor oath required. For personal study only.
β¦ Synopsis
Thoroughly revised and updated, Optimization in Drug Discovery: In Vitro Methods, Second Edition presents a wide spectrum of in vitro assays including formulation, plasma binding, absorption and permeability, cytochrome P450 (CYP) and UDP-glucuronosyltransferases (UGT) metabolism, CYP inhibition and induction, drug transporters, drug-drug interactions via assessment of reactive metabolites, genotoxicity, and chemical and photo-mutagenicity assays. Written for the Methods in Pharmacology and Toxicology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible protocols, and tips on troubleshooting and avoiding known pitfalls. Expert authors have developed and utilized these in vitro assays to achieve βdrug-likeβ characteristics in addition to efficacy properties and good safety profiles of drug candidates.
Comprehensive and up-to-date, Optimization in Drug Discovery: In Vitro Methods, Second Edition aims to guide researchers down the difficult path to successful drug discovery and development.
β¦ Table of Contents
Front Matter....Pages i-xvii
Back Matter....Pages 1-20
....Pages 21-37
β¦ Subjects
Pharmacology/Toxicology
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