Design of Enzyme Inhibitors as Drugs
Merton Sandler(Author)
Oxford University Press
Published on 1. March 1989
Book
Hardback
828 pages
978-0-19-261537-4 (ISBN)
Description
A collection of essays, based on research exploring ways in which the inhibition of the action of particular enzymes in the body can produce a desired therapeutic effect. The book contains accounts of the major target enzymes and their inhibitors which are currently the focus of research. The introductory chapters describe the underlying physical and chemical processes of enzyme inhibition and the general principles of inhibitor design using the many sophisticated and computer-based techniques that are now available. Subsequent chapters discuss in detail the wide range of individual target enzymes and inhibitors which are either in clinical use or are under study, emphasizing the factors which affect their usefulness in the clinical context - bioavailability, pharmaco kinetics and side-effects.
More details
Language
English
Place of publication
Oxford
United Kingdom
Target group
College/higher education
Professional and scholarly
Illustrations
line illustrations, colour plates, half-tone illustrations, bibliography by chapter, index
ISBN-13
978-0-19-261537-4 (9780192615374)
Copyright in bibliographic data is held by Nielsen Book Services Limited or its licensors: all rights reserved.
Schweitzer Classification
Persons
Content
Introduction to the use of enzyme inhibitors as drugs; general approaches to the design of inhibitors; inhibitors of the Renin-Angiotens in system enzymes; lactamase inhibitors; enkephalinase inhibitors as drugs; monoamine oxidase inhibitors; polyamine oxidase inhibitors; new developments in enzyme activated irreversible inhibitors of pyridoxal phosphate-dependent enzymes of therapeutic interest; cholinesterase and esterase inhibitors and reactivators of organophosphorus-inhibited esterases; inhibitors of enzymes of the arachidonic acid metabolic pathways; selective inhibitors of dihydrofolate reductases; the antibacterial sulphonamides; inhibitors of enzymes of the de novo pyrimidine pathway; inhibitors of purine biosynthesis; inhibitors of Na+, K+ ATpase; inhibitors of steriod biosynthesis; inhibitions of enzymes involved in bacterial cell wall synthesis; inhibition of proteinases; development of selective inhibitors of calmodulin-dependent phosphodiesterase and adenylate cyclase; inhibitors of carbonic anhydrase; inhibition of intracellular methyl transfer and aminopropyl transfer reactions by analogues of substrates, products, and transition states; inhibitors of some other target enzymes as potential clinical agents. Index.