Dipartimento di Chimica e Tecnologie del Farmaco, Università degli Studi di Roma La Sapienza, Ple A Moro 5, 00185 Roma, Italy.
Bioorg Med Chem. 2010 Feb;18(3):1273-9. doi: 10.1016/j.bmc.2009.12.029. Epub 2010 Jan 4.
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.
已经合成了一系列新的合成黄酮类、硫代黄酮类和黄烷酮类化合物,并将其评估为单胺氧化酶同工酶(MAO-A 和 -B)的潜在抑制剂。最活跃的系列是黄烷酮类,对 MAO-B 具有更高的选择性抑制活性。这些黄烷酮中的一些(主要是最有效的)已被分离并作为单一对映体进行测试。为了研究 MAO 对最活跃和选择性化合物的识别,使用可用的蛋白质数据库 (PDB) 结构作为对接实验的受体模型,进行了分子建模研究。