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This book covers all aspects of the medicinal chemistry of the latest drugs, and the cutting-edge science associated with them. Following the editors' 3 successful drug synthesis books, this provides expert analysis of the pros and cons of different synthetic routes and demystifies the process of modern drug discovery for practitioners and researchers.
Summarizes for each drug: respective disease area, important properties and SAR (structure-activity relationship), and chemical synthesis routes / options
Includes case studies in each chapter
Illustrates how chemistry, biology, pharmacokinetics, and a host of disciplines come together to produce successful medicines
Explains the advantages of process synthesis versus the synthetic route for drug discovery
Auteur
Jie Jack Li is an Associate Professor of chemistry at the University of San Francisco. Previously, he was a Discovery Chemist at Bristol-Myers Squibb and Pfizer. He has authored or edited over 20 books and several of those were published by Wiley, including Drug Discovery: Practices, Processes, and Perspectives, Heterocyclic Chemistry in Drug Discovery, Name Reactions in Heterocyclic Chemistry, Name Reactions for Functional Group Transformations, Contemporary Drug Synthesis, The Art of Drug Synthesis, and Modern Drug Synthesis Douglas S. Johnson is a Research Fellow and Head of Chemical Biology in the Neuroscience Medicinal Chemistry group at Pfizer Worldwide Research and Development. He is a co-author on more than 75 publications and patents and is a co-author of the book Contemporary Drug Synthesis and is an editor of The Art of Drug Synthesis, and Modern Drug Synthesis (all published by Wiley).
Contenu
Preface xi
Contributors xiii
PART I. INFECTIOUS DISEASES 1
Chapter 1. Entecavir (Baraclude): A Carbocyclic Nucleoside for the Treatment of Chronic Hepatitis B 3
1 Background 3
2 Pharmacology 5
3 StructureActivity Relationship (SAR) 6
4 Pharmacokinetics and Drug Metabolism 7
5 Efficacy and Safety 8
6 Syntheses 8
7 References 14
Chapter 2. Telaprevir (Incivek) and Boceprevir (Victrelis): NS3/4A Inhibitors for Treatment for Hepatitis C Virus (HCV) 15
1 Background 16
2 Pharmacology 16
3 StructureActivity Relationship (SAR) 17
4 PK and Drug Metabolism 20
5 Efficacy and Safety 22
6 Synthesis 24
7 Conclusions 38
8 References 39
Chapter 3. Daclatasvir (Daklinza): The First-in-Class HCV NS5A Replication Complex Inhibitor 43
1 Background 43
2 Discovery Medicinal Chemistry 45
3 Mode of Action 48
4 Pharmacokinetics and Drug Metabolism 49
5 Efficacy and Safety 49
6 Syntheses 52
7 References 57
Chapter 4. Sofosbuvir (Sovaldi): The First-in-Class HCV NS5B Nucleotide Polymerase Inhibitor 61
1 Background 61
2 Pharmacology 63
3 StructureActivity Relationship (SAR) 64
4 Pharmacokinetics and Drug Metabolism 68
5 Efficacy and Safety 69
6 Syntheses 72
7 Summary 76
8 References 76
Chapter 5. Bedaquiline (Sirturo): A Diarylquinoline that Blocks Tuberculosis ATP Synthase for the Treatment of Multi-Drug Resistant Tuberculosis 81
1 Background 81
2 Pharmacology 84
3 StructureActivity Relationship (SAR) 85
4 Pharmacokinetics and Drug Metabolism 86
5 Efficacy and Safety 87
6 Syntheses 88
7 References 96
PART II. CANCER 99
Chapter 6. Enzalutamide (Xtandi): An Androgen Receptor Antagonist for Late-Stage Prostate Cancer 101
1 Background 101
2 Pharmacology 103
3 StructureActivity Relationship (SAR) 104
4 Pharmacokinetics and Drug Metabolism 108
5 Efficacy and Safety 109
6 Synthesis 111
7 Compounds in Development 114
8 References 115
Chapter 7. Crizotinib (Xalkori): The First-in-Class ALK/ROS Inhibitor for Non-small Cell Lung Cancer 119
1 Background: Non-small Cell Lung Cancer (NSCLC) Treatment 119
2 Discovery Medicinal Chemistry Effort: SAR and Lead Optimization of Compound 2 as a c-Met Inhibitor 120
3 ALK and ROS in Non-small Cell Lung Cancer (NSCLC) Treatment 127
4 Preclinical Model Tumor Growth Inhibition Efficacy and Pharmacology 127
5 Human Clinical Trials 128
6 Introduction to the Synthesis and Limitations of the Discovery Route to Crizotinib Analogs 129
7 Process Chemistry: Initial Improvements 131
8 Process Chemistry: Enabling Route to Crizotinib 135
9 Development of the Commercial Process 141
10 Commercial Synthesis of Crizotinib 147
11 References 152
Chapter 8. Ibrutinib (Imbruvica): The First-in-Class Btk Inhibitor for Mantle Cell Lymphoma, Chronic Lymphocytic Leukemia, and Waldenstrom's Macroglobulinemia 157
1 Background 157
2 Pharmacology 159
3 StructureActivity Relationship (SAR) 159
4 Pharmacokinetics and Drug Metabolism 161
5 Efficacy and Safety 161
6 Syntheses 162
7 References 164
Chapter 9. Palbociclib (Ibrance): The First-in-Class CDK4/6 Inhibitor for Breast Cancer 167
1 Background 167
2 Pharmacology 168
3 Discovery Program 169
4 Preclinical Profile of Palbociclib 175
5 Clinical Profile of Palbociclib 176
6 Early Process Development for Palbociclib 177 7 Commercial Proces...