<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(8)</volume><submitter>Cruz-Monteagudo M</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>In the context of the current drug discovery efforts to find disease modifying therapies for Parkinson's disease (PD) the current single target strategy has proved inefficient. Consequently, the search for multi-potent agents is attracting more and more attention due to the multiple pathogenetic factors implicated in PD. Multiple evidences points to the dual inhibition of the monoamine oxidase B (MAO-B), as well as adenosine A2A receptor (A2AAR) blockade, as a promising approach to prevent the neurodegeneration involved in PD. Currently, only two chemical scaffolds has been proposed as potential dual MAO-B inhibitors/A2AAR antagonists (caffeine derivatives and benzothiazinones).&lt;h4>Methods&lt;/h4>In this study, we conduct a series of chemoinformatics analysis in order to ev</pubmed_abstract><journal>Current neuropharmacology</journal><pagination>1117-1135</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5725544</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chemoinformatics Profiling of the Chromone Nucleus as a MAO-B/A2AAR Dual Binding Scaffold.</pubmed_title><pmcid>PMC5725544</pmcid><pubmed_authors>Perera-Sardina Y</pubmed_authors><pubmed_authors>Borges F</pubmed_authors><pubmed_authors>Perez-Castillo Y</pubmed_authors><pubmed_authors>Cruz-Monteagudo M</pubmed_authors><pubmed_authors>Sanchez-Rodriguez A</pubmed_authors><pubmed_authors>Cordeiro MNDS</pubmed_authors><pubmed_authors>Helguera AM</pubmed_authors><pubmed_authors>Paz-Y-Mino C</pubmed_authors><pubmed_authors>Tejera E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chemoinformatics Profiling of the Chromone Nucleus as a MAO-B/A2AAR Dual Binding Scaffold.</name><description>&lt;h4>Background&lt;/h4>In the context of the current drug discovery efforts to find disease modifying therapies for Parkinson's disease (PD) the current single target strategy has proved inefficient. Consequently, the search for multi-potent agents is attracting more and more attention due to the multiple pathogenetic factors implicated in PD. Multiple evidences points to the dual inhibition of the monoamine oxidase B (MAO-B), as well as adenosine A2A receptor (A2AAR) blockade, as a promising approach to prevent the neurodegeneration involved in PD. Currently, only two chemical scaffolds has been proposed as potential dual MAO-B inhibitors/A2AAR antagonists (caffeine derivatives and benzothiazinones).&lt;h4>Methods&lt;/h4>In this study, we conduct a series of chemoinformatics analysis in order to ev</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Nov</publication><modification>2026-04-16T05:10:48.884Z</modification><creation>2019-03-26T23:35:56Z</creation></dates><accession>S-EPMC5725544</accession><cross_references><pubmed>28093976</pubmed><doi>10.2174/1570159X15666170116145316</doi></cross_references></HashMap>