Structure-Based Design, Synthesis, and Biological Evaluation of Novel Inhibitors of Human Cyclophilin A-Reference-Cited by-同舟云学术

Structure-Based Design, Synthesis, and Biological Evaluation of Novel Inhibitors of Human Cyclophilin A

Published:2006-01-10 Issue:3 Volume:49 Page:900-910
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Guichou Jean-François¹,Viaud Julien¹,Mettling Clément¹,Subra Guy¹,Lin Yea-Lih¹,Chavanieu Alain¹

Affiliation:

1. Centre de Biochimie Structurale, UMR 5048 CNRS, UMR 554 INSERM, UM1, Faculté de Pharmacie, BP14491, 15 Avenue Charles Flahault, 34093 Montpellier Cedex 5, France, and Institut de Génétique Humaine, Centre National de la Recherche Scientifique, Unité Propre de Recherche 1142, Montpellier Cedex 5, France

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm050716a

Reference38 articles.

1. Isolation and amino acid sequence of cyclophilin.

2. Prolyl Isomerases and Nuclear Function

3. Peptidylproline cis-trans-isomerases: immunophilins

4. Chemistry and Biology of the Immunophilins and Their Immunosuppressive Ligands

5. Peptidyl-prolyl cis-trans isomerases, a superfamily of ubiquitous folding catalysts

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