The Conformation of cyclo(−d-Pro−Ala4−) as a Model for Cyclic Pentapeptides of the dL4 Type-Reference-Cited by-同舟云学术

The Conformation of cyclo(−d-Pro−Ala4−) as a Model for Cyclic Pentapeptides of the dL4 Type

Published:2006-10-01 Issue:42 Volume:128 Page:13806-13814
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Heller Markus¹,Sukopp Martin¹,Tsomaia Natia¹,John Michael¹,Mierke Dale F.¹,Reif Bernd¹,Kessler Horst¹

Affiliation:

1. Contribution from the Department Chemie, Technische Universität München, Lichtenbergstrasse 4, 85747 Garching, Germany, Department of Molecular Pharmacology, Physiology and Biotechnology, Box B-G4, 171 Meeting Street, Brown University, Providence, Rhode Island 02912, and Forschungsinstitut für Molekulare Pharmakologie, Robert-Rössle-Strasse 10, 13125 Berlin-Buch, Germany

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja063174a

Reference36 articles.

1. Conformation of cyclic peptides. Principle concepts and the design of selectivity and superactivity in bioactive sequences by 'spatial screening'

2. Arg-Gly-Asp constrained within cyclic pentapoptides Strong and selective inhibitors of cell adhesion to vitronectin and laminin fragment P1

3. N-Methylated Cyclic RGD Peptides as Highly Active and Selective αVβ3 Integrin Antagonists

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