Advances in Amino Acid Mimetics and Peptidomimetics, Volume 1

Abell, A.

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Table of contents
  • Cover
  • ADVANCES IN AMINO ACID MIMETICS AND PEPTIDOMIMETICSiii
  • Copyright Pageiv
  • Contentsv
  • LIST OF CONTRIBUTORSvii
  • PREFACExi
  • CHAPTER 1. THE ROLE OF COMPUTER-AIDED AND STRUCTURE BASED DESIGN TECHNIQUES IN THE DISCOVERY AND OPT1
  • CHAPTER 2. MACROCYCLIC INHIBITORS OF SERINE PROTEASES41
  • CHAPTER 3. MIMICKING EXTENDED CONFORMATIONS OF PROTEASE SUBSTRATES: DESIGNING CYCLIC PEPTIDOMIMETICS77
  • CHAPTER 4. PEPTIDOMIMETIC SYNTHETIC COMBINATORIAL LIBRARIES109
  • CHAPTER 5. PEPTIDOMIMETIC LIGANDS FOR SRC HOMOLOGY-2 DOMAINS127
  • CHAPTER 6. PEPTIDOMIMETIC INHIBITORS OF FARNESYL TRANSFERASE: AN APPROACH TO NEW ANTITUMOR AGENTS165
  • CHAPTER 7. SYNTHETIC ROUTES TO LACTAM PEPTIDOMIMETICS193
  • CHAPTER 8. TOWARD RATIONALLY DESIGNED PEPTIDYL-PROLYL ISOMERASE INHIBITORS233
  • CHAPTER 9. NATURAL PRODUCT PEPTIDOMIMETICS251
  • INDEX295
Book details
  • Vendor Elsevier S & T
  • SKU 9780762302000
  • ISBN-13 9780080552620
  • Author Abell, A.
  • Category Science
  • Subject General

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Peptidomimetics are compounds which mimic the biological activity of peptides while offering the advantages of increased bioavailability, biostability, bioefficiency, and bioselectivity against the natural biological target of the parent peptide. Examples of peptidomimetics have been isolated as natural products, synthesized as libraries from novel subunits, and designed on the basis of X-ray crystallographic studies and through an intricate knowledge of the biological mode of action of natural peptides. They offer challenging synthetic targets and are increasingly important medicinal agents and biological probes. As a consequence, peptidomimetics embrace much of what is modern medicinal and organic chemistry. This volume highlights some recent and exciting developments in the area.