Description:
<jats:title>Abstract</jats:title><jats:p>Neurodegenerative disorders are becoming more prevalent given the increase in the aging population. This has inspired active research in the development of new drugs that could mark an important advance in the treatment of complex diseases such as Alzheimer′s and Parkinson′s. With the aim of finding new MAO‐B‐selective inhibitors, we report the synthesis, in vitro evaluation, and docking simulation of a new series of 3‐arylcoumarins variously substituted at the 8‐position. Most of the studied compounds show high affinity and selectivity for the hMAO‐B isoform, with IC<jats:sub>50</jats:sub> values in the low micro‐ to nanomolar range. Some of them have greater hMAO‐B inhibitory activity and selectivity than the reference compound, selegiline. Compounds <jats:bold>7</jats:bold> and <jats:bold>8</jats:bold> are the most active of this series, with compound <jats:bold>8</jats:bold> being fivefold more potent against MAO‐B and severalfold more selective than selegiline. Docking experiments were carried out with hMAO‐B crystal structures, providing new information about the enzyme–inhibitor interaction and the potential therapeutic application of the new 8‐substituted 3‐arylcoumarins.</jats:p>