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Written by the pioneers of the sildenafil (Viagra) phosphodiesterase inhibitor drug, this timely reference discusses emerging applications of novel PDE inhibitors in a variety of disease fields with contributions from major pharmaceutical companies.

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Written by the pioneers of Viagra, the first blockbuster PDE inhibitor drug.
Beginning with a review of the first wave of phosphodiesterase (PDE) inhibitors, this book focuses on new and emerging PDE targets and their inhibitors. Drug development options for all major human PDE families are discussed and cover diverse therapeutic fields, such as neurological/psychiatric, cardiovascular/metabolic, pain, and allergy/respiratory diseases. Finally, emerging chemotherapeutic applications of PDE inhibitors against malaria and other tropical diseases are discussed.

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INTRODUCTION

TOWARD A NEW GENERATION OF PDE5 INHIBITORS THROUGH ADVANCES IN MEDICINAL CHEMISTRY
Introduction
The First-Generation Agents
PDE5 as a Mechanism and Alternative Indications Beyond MED
A Summary of PDE5 Chemotypes Reported Post-2010
Second-Generation PDE5 Inhibitors from Pfizer: Pyrazolopyrimidines
Second-Generation PDE5 Inhibitors from Pfizer: Pyridopyrazinones
Conclusions

PDE4: NEW STRUCTURAL INSIGHTS INTO A REGULATORY MECHANISM AND IMPLICATIONS FOR THE DESIGN OF SELECTIVE INHIBITORS
Introduction
Isoforms, Domain Organizations, and Splice Variants
Structural Features of the Catalytic Site
Regulation of PDE4 Activity
Crystal Structure of Regulatory Domains of PDE4
URC2 Interaction and Selectivity
Conclusions

PDE4: RECENT MEDICINAL CHEMISTRY STRATEGIES TO MITIGATE ADVERSE EFFECTS
Introduction
Brief Summary of pan-PDE4 Inhibitors
PDE4 Strategies to Avoid Gastrointestinal Events
Conclusions

THE FUNCTION, ENZYME KINETICS, STRUCTURAL BIOLOGY, AND MEDICINAL CHEMISTRY OF PDE10A
Enzymology and Protein Structure
Papaverine-Related PDE10A Inhibitors
MP-10/PF-2545920 Class of InhibitorsPF-2545920/MP-Inspired Inhibitors
PF-2545920/Papaverine/Quinazoline Hybrid Series of Inhibitors
PET Ligand Development
Summary and Future

THE STATE OF THE ART IN SELECTIVE PDE2A INHIBITOR DESIGN
Introduction
Selective PDE2A Inhibitors
Methods
Conclusions

CRYSTAL STRUCTURES OF PHOSPHODIESTERASE 9A AND INSIGHT INTO INHIBITOR DISCOVERY
Introduction
Subtle Asymmetry of the PDE9 Dimer in the Crystals
The Structure of the PDE9 Catalytic Domain
Interaction of Inhibitors with PDE9
Implication on Inhibitor Selectivity

PDEs AS CNS TARGETS: PDE9 INHIBITORS FOR COGNITIVE DEFICIT DISEASES
PDE9A Enzymology and Pharmacology
Crystal Structures of PDE9A Inhibitors
Medicinal Chemistry Efforts toward Identifying PDE9A Inhibitors for Treating Cognitive Disorders
Analysis of CNS Desireability of PDE9A Inhibitors
Conclusions

PHOSPHODIESTERASE 8B
Introduction
Identification
Properties
Expression and Tissue Distribution
Functions of PDE8B
Inhibitors and Potential Therapeutic Uses

SELECTIVE NEW SMALL-MOLECULE INHIBITORS OF PHOSPHODIESTERASE 1
Introduction
PDE1 Enzymology
PDe1 Inhibitors
Conclusion

RECENT ADVANCES IN THE DEVELOPMENT OF PDE7 INHIBITORS
Introduction
Historical Development of PDE7 Inhibitors
Recent Advances in the Discovery of PDE7 Inhibitors for Peripheral Therapeutic Benefit
Recent Advances in the Discovery of PDE7 Inhibitors for CNS-Related Disorders
Recent Advances in the Discovery of Dual PDE7 Inhibitors
Identifying Next-Generation PDE7 Inhibitors
Summary

INHIBITORS OF PROTOZOAN PHOSPHODIESTERASES AS POTENTIAL THERAPEUTIC APPROACHES FOR TROPICAL DISEASES
Introduction
Malaria
Chagas Disease
Leishmaniasis
Human African Trypanosomiasis
Conclusion

Index

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