Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367464 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
Abstract
Fenobam (1) was developed by McNeil Laboratories as an anxiolytic agent with an unknown molecular target in the late 1970s. In a recent publication, it was revealed that fenobam is a non-competitive mGluR5 antagonist. Herein, we present the structure–activity relationship of fenobam and its analogues and similarities between the SAR of mGluR5 antagonism and the SAR of CNS properties originally reported by McNeil are discussed.
Graphical abstractStructure–activity relationship of the mGluR5 antagonist fenobam is reported.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Andreas Wållberg, Karolina Nilsson, Krister Österlund, Alecia Peterson, Susanne Elg, Patrick Raboisson, Udo Bauer, Lance G. Hammerland, Jan P. Mattsson,