<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(8)</volume><submitter>Pedras MSC</submitter><pubmed_abstract>The detoxification of the phytoalexin brassinin to indole-3-carboxaldehyde and &lt;i>S&lt;/i>-methyl dithiocarbamate is catalyzed by brassinin oxidase (BOLm), an inducible fungal enzyme produced by the plant pathogen &lt;i>Leptosphaeria maculans&lt;/i>. Twenty-six substituted quinolines and isoquinolines are synthesized and evaluated for antifungal activity against &lt;i>L. maculans&lt;/i> and inhibition of BOLm. Eleven compounds that inhibit BOLm activity are reported, of which 3-ethyl-6-phenylquinoline displays the highest inhibitory effect. In general, substituted 3-phenylquinolines show significantly higher inhibitory activities than the corresponding 2-phenylquinolines. Overall, these results indicate that the quinoline scaffold is a good lead to design paldoxins (phytoalexin detoxification inhibitors)</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pagination>E1345</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6152025</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Inhibitors of the Detoxifying Enzyme of the Phytoalexin Brassinin Based on Quinoline and Isoquinoline Scaffolds.</pubmed_title><pmcid>PMC6152025</pmcid><pubmed_authors>Abdoli A</pubmed_authors><pubmed_authors>Sarma-Mamillapalle VK</pubmed_authors><pubmed_authors>Pedras MSC</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inhibitors of the Detoxifying Enzyme of the Phytoalexin Brassinin Based on Quinoline and Isoquinoline Scaffolds.</name><description>The detoxification of the phytoalexin brassinin to indole-3-carboxaldehyde and &lt;i>S&lt;/i>-methyl dithiocarbamate is catalyzed by brassinin oxidase (BOLm), an inducible fungal enzyme produced by the plant pathogen &lt;i>Leptosphaeria maculans&lt;/i>. Twenty-six substituted quinolines and isoquinolines are synthesized and evaluated for antifungal activity against &lt;i>L. maculans&lt;/i> and inhibition of BOLm. Eleven compounds that inhibit BOLm activity are reported, of which 3-ethyl-6-phenylquinoline displays the highest inhibitory effect. In general, substituted 3-phenylquinolines show significantly higher inhibitory activities than the corresponding 2-phenylquinolines. Overall, these results indicate that the quinoline scaffold is a good lead to design paldoxins (phytoalexin detoxification inhibitors)</description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 Aug</publication><modification>2026-06-10T09:26:34.922Z</modification><creation>2026-06-10T03:12:10.609Z</creation></dates><accession>S-EPMC6152025</accession><cross_references><pubmed>28805743</pubmed><doi>10.3390/molecules22081345</doi></cross_references></HashMap>