Inside Back Cover: Fine-tuning the π-π Aromatic Interactions in Peptides: Somatostatin Analogues Containing Mesityl Alanine (Angew. Chem. Int. Ed. 8/2012)

The π–π aromatic interactions between amino acids 6, 7, and 11 in the natural hormone somatostatin are crucial for conformational stability. In their Communication on page 1820 ff., M. J. Macias, A. Riera, and co‐workers describe that peptidic analogues obtained by replacing each phenylalanine with...

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Veröffentlicht in:Angewandte Chemie International Edition 2012-02, Vol.51 (8), p.1977-1977
Hauptverfasser: Martín-Gago, Pablo, Gomez-Caminals, Marc, Ramón, Rosario, Verdaguer, Xavier, Martin-Malpartida, Pau, Aragón, Eric, Fernández-Carneado, Jimena, Ponsati, Berta, López-Ruiz, Pilar, Cortes, Maria Alicia, Colás, Begoña, Macias, Maria J., Riera, Antoni
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container_end_page 1977
container_issue 8
container_start_page 1977
container_title Angewandte Chemie International Edition
container_volume 51
creator Martín-Gago, Pablo
Gomez-Caminals, Marc
Ramón, Rosario
Verdaguer, Xavier
Martin-Malpartida, Pau
Aragón, Eric
Fernández-Carneado, Jimena
Ponsati, Berta
López-Ruiz, Pilar
Cortes, Maria Alicia
Colás, Begoña
Macias, Maria J.
Riera, Antoni
description The π–π aromatic interactions between amino acids 6, 7, and 11 in the natural hormone somatostatin are crucial for conformational stability. In their Communication on page 1820 ff., M. J. Macias, A. Riera, and co‐workers describe that peptidic analogues obtained by replacing each phenylalanine with mesitylalanine are conformationally more rigid than the parent hormone. This strategy has yielded the first 3D structures of 14‐amino‐acid somatostatin analogues.
doi_str_mv 10.1002/anie.201108928
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source Wiley Online Library Journals Frontfile Complete
subjects conformation analysis
drug design
NMR spectroscopy
noncovalent interactions
peptides
title Inside Back Cover: Fine-tuning the π-π Aromatic Interactions in Peptides: Somatostatin Analogues Containing Mesityl Alanine (Angew. Chem. Int. Ed. 8/2012)
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