Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1377016 | Bioorganic & Medicinal Chemistry Letters | 2006 | 6 Pages |
Abstract
A novel series of N,N′-bis[2-oxo-2H-1-benzopyran]-3-carboxamide derivatives have been synthesized and investigated for the ability to inhibit the activity of the A and B isoforms of monoamine oxidase (MAO). Some of the synthesized compounds show good selective inhibitory activity against the MAO-A isoform. Both the MAO-A and -B isoforms, deposited in the Protein Data Bank as the 2BXR and 1GOS models, respectively, were considered in a computational study performed with docking techniques on the most active and selective inhibitors.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Franco Chimenti, Daniela Secci, Adriana Bolasco, Paola Chimenti, Arianna Granese, Simone Carradori, Olivia Befani, Paola Turini, Stefano Alcaro, Francesco Ortuso,