| Literature DB >> 20045650 |
Franco Chimenti1, Rossella Fioravanti, Adriana Bolasco, Paola Chimenti, Daniela Secci, Francesca Rossi, Matilde Yáñez, Francisco Orallo, Francesco Ortuso, Stefano Alcaro, Roberto Cirilli, Rosella Ferretti, M Luisa Sanna.
Abstract
A new series of synthetic flavones, thioflavones, and flavanones has been synthesized and evaluated as potential inhibitors of monoamine oxidase isoforms (MAO-A and -B). The most active series is the flavanone one with higher selective inhibitory activity against MAO-B. Some of these flavanones (mainly the most effective) have been separated and tested as single enantiomers. In order to investigate the MAOs recognition of the most active and selective compounds, a molecular modeling study has been performed using available Protein Data Bank (PDB) structures as receptor models for docking experiments. Copyright (c) 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2010 PMID: 20045650 DOI: 10.1016/j.bmc.2009.12.029
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641