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BACE : Lead Target for Orchestrated Therapy of Alzheimer's Disease - Varghese John

BACE

Lead Target for Orchestrated Therapy of Alzheimer's Disease

By: Varghese John

Hardcover | 16 February 2010 | Edition Number 1

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BACE inhibitors and their use in the treatment of Alzheimer's Disease

BACE (ß-site of APP cleaving enzyme) is a critical component in Alzheimer's Disease (AD), and the development of BACE inhibitors shows great potential as a therapy for the disease. BACE: Lead Target for Orchestrated Therapy of Alzheimer's Disease covers virtually all aspects of BACE from initial identification, discovery of inhibitors, and challenges in clinical development, while providing a global understanding essential for productive and successful drug discovery.

This book details the story of the discovery of BACE and its role in AD and comprehensively discusses:

  • The development of BACE inhibitors as therapeutics for Alzheimer's disease

  • The research that led to the identification of BACE

  • New BACE inhibitors currently being clinically tested

  • ADME (absorption, distribution, metabolism, excretion) and clinical trial design-topics not addressed in current field literature

  • Cutting-edge technology such as high-throughput screening, structure-based drug design, and QSAR in context of BACE inhibitors and Alzheimer's drug discovery

  • Other approaches to BACE inhibition based on interaction with the precursor protein APP

By enhancing the reader's understanding of the various aspects of the BACE drug-discovery process, this much-needed reference will serve as a key resource for all scientists involved in Alzheimer's research-and inspire new approaches to treatment of AD.

Industry Reviews
"Overall this book is a timely and comprehensive resource covering developments in BACE-targeted therapeutic agents from infancy to the present time. It will prove to be valuable to researchers working in the AD field, as well as to medicinal chemists seeking to learn more about rational design of aspartyl protease inhibitors." (ChemMedChem, November 2010)

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