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.
journal_name
Bioorg Med Chemjournal_title
Bioorganic & medicinal chemistryauthors
Chimenti F,Fioravanti R,Bolasco A,Chimenti P,Secci D,Rossi F,Yáñez M,Orallo F,Ortuso F,Alcaro S,Cirilli R,Ferretti R,Sanna MLdoi
10.1016/j.bmc.2009.12.029subject
Has Abstractpub_date
2010-02-01 00:00:00pages
1273-9issue
3eissn
0968-0896issn
1464-3391pii
S0968-0896(09)01113-4journal_volume
18pub_type
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