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A new series of flavones, thioflavones, and flavanones as selective monoamine oxidase-B inhibitors.
- Source :
-
Bioorganic & medicinal chemistry [Bioorg Med Chem] 2010 Feb; Vol. 18 (3), pp. 1273-9. Date of Electronic Publication: 2010 Jan 04. - Publication Year :
- 2010
-
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.<br /> (Copyright (c) 2009 Elsevier Ltd. All rights reserved.)
- Subjects :
- Flavanones chemical synthesis
Flavones chemical synthesis
Humans
Models, Molecular
Monoamine Oxidase chemistry
Monoamine Oxidase Inhibitors chemical synthesis
Stereoisomerism
Sulfhydryl Compounds chemistry
Flavanones chemistry
Flavanones pharmacology
Flavones chemistry
Flavones pharmacology
Monoamine Oxidase metabolism
Monoamine Oxidase Inhibitors chemistry
Monoamine Oxidase Inhibitors pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1464-3391
- Volume :
- 18
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Bioorganic & medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 20045650
- Full Text :
- https://doi.org/10.1016/j.bmc.2009.12.029