The Combination of Prolinoamino Acids and Cyclopropylamino Acids Leads to Fully Functionalized, Stable β-Turns in Water-Reference-Cited by-同舟云学术

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The Combination of Prolinoamino Acids and Cyclopropylamino Acids Leads to Fully Functionalized, Stable β-Turns in Water

Published:2011-03-29 Issue:7 Volume:12 Page:1039-1042
ISSN:1439-4227
Container-title:ChemBioChem
language:en
Short-container-title:ChemBioChem

Author:

Guitot Karine,Larregola Maud,Pradhan Tarun K.,Vasse Jean-Luc,Lavielle Solange,Bertus Philippe,Szymoniak Jan,Lequin Olivier,Karoyan Philippe

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

Reference46 articles.

1. β-Turn Preferences Induced by 2,3-Methanophenylalanine Chirality

2. Exploring Ramachandran and Chi Space: Conformationally Constrained Amino Acids and Peptides in the Design of Bioactive Polypeptide Ligands

3. N-Methylation of Peptides: A New Perspective in Medicinal Chemistry

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1. Interfering peptides targeting protein–protein interactions: the next generation of drugs?;Drug Discovery Today;2018-02

2. A Short Access to Symmetrically α,α-Disubstituted α-Amino Acids from Acyl Cyanohydrins;Synthesis;2016-01-13

3. Titanium-Mediated Cyclopropanation of Nitriles with Unsaturated Grignard Reagents: Application to the Synthesis of Constrained Lysine Derivatives;Synthesis;2015-01-28

4. Synthesis and conformational studies of a stable peptidomimetic β-hairpin based on a bifunctional diketopiperazine turn inducer;New Journal of Chemistry;2015

5. Proline-glutamate chimera’s side chain conformation directs the type of β-hairpin structure;Amino Acids;2013-11-13

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