| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1376730 | Bioorganic & Medicinal Chemistry Letters | 2006 | 5 Pages |
Abstract
Substituted (thio)hydantoins (2-thioxoimidazolidinones and imidazolidinediones) were reported as new potential reversible inhibitors of fatty acid amide hydrolase (FAAH). Their binding mode to FAAH was explored to rationalize their activity and give idea to design highly active inhibitors. Starting from the crystal structure of one of these molecules, docking studies provide us with rational basis for the design of new inhibitors within the thiohydantoin family.
Graphical abstractThe binding mode of new (thio)hydantoin FAAH inhibitors is reported and compared with the one of known reference compounds. This study gives ideas to design more active compounds.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Catherine Michaux, Giulio G. Muccioli, Didier M. Lambert, Johan Wouters,