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 |
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container_end_page | 1977 |
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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 |
format | Article |
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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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