Published January 1980
by John Wiley & Sons Inc .
Written in English
|The Physical Object|
|Number of Pages||178|
Synthetic Peptides discusses racemization, protecting group techniques, peptide bond-forming methodology, amino acids, and dipeptide syntheses. The book explains solid phase synthesis methods, cyclopeptides, nucleopeptides, chromopeptides of the actinomycin D type, and cites examples of syntheses of peptides of different sizes. Synthesis of biologically active cyclic peptides. Nobuo Izumiya. Laboratory of Biochemistry, Faculty of Science, Kyushu Univers Hakozaki, Higashi‐ku, Fukuoka , Japan Synthetic Strategies for Macrocyclic Peptides, Practical Medicinal An efficient strategy for the large-scale synthesis of head-to-tail cyclic peptides, Letters Cited by: Many biologically active peptides of the immune system like cytokines and chemokines are generated or inactivated by a concerted action of proteolytic enzymes. One of the most prominent peptidases is the dipeptidyl aminopeptidase IV (DP IV, CD26, EC ), which is expressed on all lymphocytes and that plays a crucial role in regulation of. Recent Progress of the Synthetic Studies of Biologically Active Marine Cyclic Peptides and Depsipeptides. ChemInform , 37 (17) DOI: /chin Ian R. Baxendale, Steven V. Ley, Christopher D. Smith, Geoffrey K. by:
Buy Synthetic Aspects of Biologically Active Cyclic Peptides by Nobuo Izumiya, etc. from Waterstones today! Click and Collect from your local Waterstones Pages: Solid-phase synthesis. The established method for the production of synthetic peptides in the lab is known as solid-phase peptide synthesis (SPPS). Pioneered by Robert Bruce Merrifield, SPPS allows the rapid assembly of a peptide chain through successive reactions of amino acid derivatives on an insoluble porous support.. The solid support consists of small, polymeric resin beads. The authors explain the broad fundamentals of peptide synthesis and structure, systematically addressing important families of biologically active peptides, and adopting an interdisciplinary approach that covers application areas in biotechnology, pharmaceutical science, and . Handbook of Biologically Active Peptides, Second Edition, is the definitive, indispensable reference for peptide researchers, biochemists, cell and molecular biologists, neuroscientists, pharmacologists, and endocrinologists. Its chapters are designed to be a source for workers in the field and enable researchers working in a specific area to examine related areas outside their Edition: 2.
This book introduces cyclic peptides and provides a thorough overview of biosynthetic and fully synthetic approaches to their preparation. Following an introduction to cyclic peptides, biosynthetic and traditional chemical routes to cyclic peptides are reviewed. Due to their size, their synthesis is not : $ AFPep is a cyclic anti-cancer peptide. Earlier we elaborated an inexpensive, synthetic, 9-amino acid cyclic peptide that is useful for the treatment or prevention of breast cancer in animal models, and which retains activity after oral administration [2, 11, 25, 29, 30].We call this peptide AFPep because it is a peptide mimic of the anti-oncogenic active site of α-fetoprotein (AFP, a Cited by: 9. Synthetic Peptides discusses racemization, protecting group techniques, peptide bond-forming methodology, amino acids, and dipeptide syntheses. The book explains solid phase synthesis methods, cyclopeptides, nucleopeptides, chromopeptides of the actinomycin D type, and cites examples of syntheses of peptides of different Edition: 1. Susceptibilities of Mycoplasma fermentans and Mycoplasma hyorhinis to Membrane-Active Peptides and Enrofloxacin in Human Tissue Cell Cultures. In Synthetic aspects of biologically active cyclic peptides. Kodansha, Tokyo, Japan, and Halsted Press, New York, N.Y. Cited by: