Peptides Constrained by an Aliphatic Linkage between Two Cα Sites: Design, Synthesis, and Unexpected Conformational Properties of an i,(i + 4)-Linked Peptide-Reference-Cited by-同舟云学术

Peptides Constrained by an Aliphatic Linkage between Two Cα Sites: Design, Synthesis, and Unexpected Conformational Properties of an i,(i + 4)-Linked Peptide

Published:2001-06-01 Issue:13 Volume:66 Page:4585-4594
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alexander McNamara Linda M.¹,Andrews Martin J. I.¹,Mitzel Frieder¹,Siligardi Giuliano¹,Tabor Alethea B.¹

Affiliation:

1. Department of Chemistry, University College London, Christoper Ingold Laboratories, 20 Gordon Street, London WC1H 0AJ, U.K., and Department of Pharmacy, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London SE1 8WA, U.K.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo015508e

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1. Stereoisomeric Peptide Libraries and Peptidomimetics for Designing Selective Inhibitors of theαvβ3 Integrin for a New Cancer Therapy

2. Concepts and progress in the development of peptide mimetics

3. Peptidomimetics for Receptor Ligands?Discovery, Development, and Medical Perspectives

4. Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics

5. Emerging approaches in the molecular design of receptor-selective peptide ligands: conformational, topographical and dynamic considerations

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