Diversity-Oriented Synthesis of Cyclic Azapeptides by A3-Macrocyclization Provides High-Affinity CD36-Modulating Peptidomimetics-Reference-Cited by-同舟云学术

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Diversity-Oriented Synthesis of Cyclic Azapeptides by A3-Macrocyclization Provides High-Affinity CD36-Modulating Peptidomimetics

Published:2017-01-16 Issue:22 Volume:56 Page:6284-6288
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Zhang Jinqiang¹²^ORCID,Mulumba Mukandila³,Ong Huy³,Lubell William D.¹^ORCID

Affiliation:

1. Département de Chimie; Université de Montréal; C.P. 6128, Succursale Centre-Ville Montréal Québec H3C 3J7 Canada

2. Present address: School of Pharmaceutical Science; Chongqing University; Chongqing 401331 China

3. Faculté de Pharmacie; Université de Montréal; C.P. 6128, Succursale Centre-Ville Montréal Québec H3C 3J7 Canada

Funder

Natural Sciences and Engineering Research Council of Canada

Canadian Institutes of Health Research

Ministère du développement économique de l'innovation et de l'exportation du Quebec

Amorchem

NSERC-CIHR collaborative health research project (CHRP)

Publisher

Wiley

Subject

General Chemistry,Catalysis

Reference70 articles.

1. Macrocycles Are Great Cycles: Applications, Opportunities, and Challenges of Synthetic Macrocycles in Drug Discovery

2. The Future of Peptide-based Drugs

3. Conformation and Biological Activity of Cyclic Peptides

4. Contemporary strategies for the stabilization of peptides in the α-helical conformation

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