Trifluoromethylated Proline Surrogates as Part of “Pro–Pro” Turn‐Inducing Templates-Reference-Cited by-同舟云学术

Trifluoromethylated Proline Surrogates as Part of “Pro–Pro” Turn‐Inducing Templates

Published:2019-07-15 Issue:19 Volume:20 Page:2513-2518
ISSN:1439-4227
Container-title:ChemBioChem
language:en
Short-container-title:ChemBioChem

Author:

Gadais Charlène¹^ORCID,Van holsbeeck Kevin¹²^ORCID,Moors Samuel L. C.³,Buyst Dieter²,Fehér Krisztina²,Van Hecke Kristof⁴^ORCID,Tourwé Dirk¹,Brigaud Thierry⁵^ORCID,Martin Charlotte¹^ORCID,De Proft Frank³^ORCID,Pytkowicz Julien⁵,Martins José C.²^ORCID,Chaume Grégory⁵^ORCID,Ballet Steven¹^ORCID

Affiliation:

1. Research Group of Organic ChemistryDepartments of Bioengineering Sciences and ChemistryVrije Universiteit Brussel Pleinlaan 2 1050 Brussels Belgium

2. NMR and Structure Analysis UnitDepartment of Organic and Macromolecular ChemistryGhent University Krijgslaan 281 9000 Gent Belgium

3. Eenheid Algemene Chemie (ALGC)Department of ChemistryVrije Universiteit Brussel Pleinlaan 2 1050 Brussels Belgium

4. XStruct Bio-Inorganic Group, Department of ChemistryGhent University Krijgslaan 281 9000 Gent Belgium

5. Laboratoire de Chimie BiologiqueUniversité de Cergy–Pontoise 5 Mail Gay-Lussac 95031 Cergy-Pontoise cedex France

Funder

Fonds Wetenschappelijk Onderzoek

Hercules Foundation

Bijzonder Onderzoeksfonds

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cbic.201900294

Reference34 articles.

1. Structure-Based Design of Inhibitors of Protein-Protein Interactions: Mimicking Peptide Binding Epitopes

2. Strukturbasierte Entwicklung von Protein-Protein-Interaktionsinhibitoren: Stabilisierung und Nachahmung von Peptidliganden

3. The design, structures and therapeutic potential of protein epitope mimetics

4. β-Hairpin protein epitope mimetic technology in drug discovery

5. β-Hairpin Peptidomimetics: Design, Structures and Biological Activities

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