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003 OCoLC
005 20190328114812.0
006 m o d
007 cr cnu---unuuu
008 150709s2015 enk o 001 0 eng d
040 _aOPELS
_beng
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019 _a913694294
_a920816765
_a959423590
020 _a9780124172135
_q(electronic bk.)
020 _a012417213X
_q(electronic bk.)
020 _z9780124172050
020 _z0124172059
035 _a(OCoLC)913530203
_z(OCoLC)913694294
_z(OCoLC)920816765
_z(OCoLC)959423590
050 4 _aRS403
060 4 _aQV 744
072 7 _aMED
_x071000
_2bisacsh
082 0 4 _a615.1/9
_223
245 0 4 _aThe practice of medicinal chemistry /
_h[electronic resource]
_cedited by Camille Georges Wermuth, David Aldous, Pierre Raboisson, Didier Rognan.
250 _a4th ed.
264 1 _aLondon, UK :
_bAcademic Press,
_c2015.
300 _a1 online resource
336 _atext
_btxt
_2rdacontent
337 _acomputer
_bc
_2rdamedia
338 _aonline resource
_bcr
_2rdacarrier
520 _aThe Practice of Medicinal Chemistry, Fourth Edition, provides a practical and comprehensive overview of the daily issues facing pharmaceutical researchers and chemists. In addition to its thorough and excellent treatment of basic medicinal chemistry principles, this updated edition has been thoroughly revised to provide new and expanded coverage of the latest technologies and approaches in drug discovery. With in-depth coverage of high content screening, scoring, docking, binding free energy calculations, polypharmacology, QSAR, chemical collections and databases, and much more, this book is the go-to reference for all academic and pharmaceutical researchers who need a complete understanding of medicinal chemistry and its application to drug discovery and development.
500 _aIncludes index.
588 0 _aOnline resource; title from PDF title page (ScienceDirect, viewed July 9, 2015).
505 0 _aFront Cover; The Practice of Medicinal Chemistry; Copyright Page; Contents; List of Contributors; Foreword; Preface to the Fourth Edition; Preface to the Third Edition; Preface to the Second Edition; Preface to the First Edition; I. General Aspects of Medicinal Chemistry; 1 Medicinal Chemistry: Definitions and Objectives, Drug Activity Phases, Drug Classification Systems; I. Definitions and Objectives; A Medicinal Chemistry and Related Disciplines and Terms; B Drugs and Drug Substances; C Stages of Drug Development; II. Drug Activity Phases; A The Pharmaceutical Phase.
505 8 _aB The Pharmacokinetic PhaseC The Pharmacodynamic Phase; D The Road to Successful Drug Development?; III. Drug Classification Systems; A Classification by Target and Mechanism of Action; 1 Targets; 2 Mechanisms of Action; B Other Classification Systems; References; 2 Evaluation of the Biological Activity of Compounds: Techniques and Mechanism of Action Studies; I. Introduction; II. Drug Discovery Approaches and Screening Cascades; A Target Based Screening; B Phenotypic Screening; III. In Vitro Assays; A Primary Assays; Glossary; 1 Binding assays; 2 Binding Studies: Principles and Analysis.
505 8 _a3 Enzyme Assays4 Types of Enzyme Inhibition and Their Analysis; A Reversible Inhibitors; B Irreversible Inhibitors; C Competitive Inhibitors; D Noncompetitive Inhibitors; E Uncompetitive Inhibitors; 5 Functional Assays; 6 Functional Studies and Their Analysis; A Agonist Concentration-Effect (E/[A]) Curves; B Full Agonists, Partial Agonists, and Inverse Agonists; C Optimizing Agonists; D Analysis of Antagonists; Competitive Antagonists; Irreversible, Noncompetitive, and Allosteric Antagonists; B Compound Interference in Primary Assays: Artifacts and False Positives; C Assay Biostatistics.
505 8 _aD Selectivity, Cytotoxicity, and Species Cross-over. 1 Selectivity; 2 Cytotoxicity; 3 Species Crossover; E Cellular and Tissue Functional Responses; IV. Ex Vivo Assays; V. In Vivo Assays; A Pharmacokinetic Models; B Efficacy Models; C Safety Testing; Acknowledgements; References; 3 Drug Targets, Target Identification, Validation, and Screening; I. Introduction; II. What is a Drug Target?; III. The Purpose of Target Identification; A Target-Based Screening; B Phenotypic Screening; C Fast Follower Strategy; IV. Target Options and Treatment Options; V. Target Deconvolution and Target Discovery.
505 8 _aVI. Methods for Target Identification and ValidationA Affinity Chromatography; B Genetic Methods; C Haploinsufficiency Profiling in Yeast; D Analysis of Resistant Mutants; E siRNA for Target Validation; F Yeast Three-Hybrid System; G DNA Microarrays; H Comparative Profiling; I Analysis of the Pathophysiology; J The Study of Existing Drugs; K Systems Biology; L In Silico Simulation of the Human Patient; VII. Target Validation; VIII. Conclusion; References; II. Lead Compound Discovery Strategies; 4 Strategies in the Search for New Lead Compounds or Original Working Hypotheses; I. Introduction.
504 _aIncludes bibliographical references and index.
588 0 _aPrint version record.
650 0 _aPharmaceutical chemistry.
650 0 _aDrugs
_xDesign.
650 7 _aDrugs
_xDesign.
_2fast
_0(OCoLC)fst00898790
650 7 _aPharmaceutical chemistry.
_2fast
_0(OCoLC)fst01060115
650 7 _aMEDICAL / Pharmacology.
_2bisacsh
655 4 _aElectronic books.
655 0 _aElectronic books.
700 1 _aWermuth, C. G.,
_eeditor.
700 1 _aAldous, David
_q(David John),
_eeditor.
700 1 _aRaboisson, Pierre,
_eeditor.
700 1 _aRognan, Didier,
_eeditor.
776 0 8 _iPrint version:
_tPractice of medicinal chemistry.
_bFourth edition.
_dLondon, UK : Academic Press, 2015
_z9780124172050
856 4 0 _3ScienceDirect
_uhttp://www.sciencedirect.com/science/book/9780124172050
999 _c247114
_d247114