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Inhibitors of molecular chaperones as therapeutic agents / edited by Timothy Machajewski and Zhenhai Gao, Novartis, California, USA.

Contributor(s): Material type: TextTextSeries: RSC drug discovery series ; 37.Publisher: Cambridge : RSC Publishing, [2014]Description: xvi, 425 pages : illustrations (some color) ; 24 cmContent type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
ISBN:
  • 9781849736664
  • 1849736669
Subject(s): DDC classification:
  • 572.645 23
LOC classification:
  • QP552.M64 I54 2014
NLM classification:
  • 2014 D-722
  • QU 55.6
Summary: This book aims to provide a comprehensive examination of the field of molecular chaperone inhibition and its application to pharmaceutical research. With several small molecule inhibitors in oncology clinical development, there is clearly intense interest in the chaperones as a molecular target. Filling a significant gap in the market by providing a detailed comparison of discovery programs across the industry, this text will find broad interest among researchers in the field of molecular chaperone pharmaceutical research, oncology research, and medicinal chemistry. Arranged into three main sections the book covers structure and function, small molecule inhibitors and concludes with a section discussing clinical perspectives. With specific chapters covering the discovery of key molecules such as, BIIB028, STA-9090, Serenex Hsp90 inhibitor, NVP-AUY922 and NVP-HSP990, this comprehensive text will be an essential treatise for researchers working in academia and industry.-- Source other than Library of Congress.
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Holdings
Item type Current library Collection Call number Status Date due Barcode
Books Books Main Library General Stacks Non-fiction 572.645 INH (Browse shelf(Opens below)) Available MUL17021980

Includes bibliographical references and index.

This book aims to provide a comprehensive examination of the field of molecular chaperone inhibition and its application to pharmaceutical research. With several small molecule inhibitors in oncology clinical development, there is clearly intense interest in the chaperones as a molecular target. Filling a significant gap in the market by providing a detailed comparison of discovery programs across the industry, this text will find broad interest among researchers in the field of molecular chaperone pharmaceutical research, oncology research, and medicinal chemistry. Arranged into three main sections the book covers structure and function, small molecule inhibitors and concludes with a section discussing clinical perspectives. With specific chapters covering the discovery of key molecules such as, BIIB028, STA-9090, Serenex Hsp90 inhibitor, NVP-AUY922 and NVP-HSP990, this comprehensive text will be an essential treatise for researchers working in academia and industry.-- Source other than Library of Congress.

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