Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1378260 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
Abstract
Following the recent disclosure of 3-methyl pyrrole-2,4-dicarboxylic acid 2-propyl ester 4-(1,2,2-trimethyl-propyl) ester as a potent and selective mGluR1 non-competitive antagonist, the use of a doubly 13C-labeled analogue to identify, and consequently prevent, metabolically labile positions is reported.
Graphical abstractInvestigation on the metabolic fate of the pyrrole mGluR1 antagonist class is presented.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Fabrizio Micheli, Paolo Cavanni, Romano Di Fabio, Daniele Donati, Mahmoud Hamdan, Stefano Provera, Maria Elvira Tranquillini, Giovanni Vitulli,