Influence of ring substitution on the conformation and β-turn mimicry of 4-amino-1,2,4,5-tetrahydro-2-benzazepin-3-one peptide mimetics-Reference-Cited by-同舟云学术

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Influence of ring substitution on the conformation and β-turn mimicry of 4-amino-1,2,4,5-tetrahydro-2-benzazepin-3-one peptide mimetics

Published:2009-03 Issue:11 Volume:65 Page:2266-2278
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

De Wachter Rien,Brans Luc,Ballet Steven,Van den Eynde Isabelle,Feytens Debby,Keresztes Attila,Toth Geza,Urbanczyk-Lipkowska Zofia,Tourwé Dirk

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference65 articles.

1. Over One Hundred Peptide-Activated G Protein-Coupled Receptors Recognize Ligands with Turn Structure

2. Prediction of Tight Turns and Their Types in Proteins

3. β-Turn mimetic library synthesis: scaffolds and applications

4. Design, synthesis, and application of azabicyclo[X.Y.0]alkanone amino acids as constrained dipeptide surrogates and peptide mimics

5. Design and synthesis of novel type VI-like β-turn mimetics. Diversity at the i+1 and the i+2 position

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2. Rapid and Mild Lactamization Using Highly Electrophilic Triphosgene in a Microflow Reactor;Chemistry – A European Journal;2021-03-08

3. Design, synthesis and biological evaluation of novel 2-(5-aryl-1H-imidazol-1-yl) derivatives as potential inhibitors of the HIV-1 Vpu and host BST-2 protein interaction;European Journal of Medicinal Chemistry;2020-03

4. Efficient One-Pot Access to Trisubstituted 2-Benzazepin-3-ones as Constrained Pseudopeptide Analogues and Privileged Scaffolds;Medicinal Chemistry;2018-05-11

5. Side Chain Cyclized Aromatic Amino Acids: Great Tools as Local Constraints in Peptide and Peptidomimetic Design;Journal of Medicinal Chemistry;2016-10-12

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