<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Shi H</submitter><pubmed_abstract>Three new antibacterial spirooxindole alkaloids, spirobrefeldins A-C (1-3), together with four known analogs, spirotryprostatin M (4), spirotryprostatin G (5), 12β-hydroxyverruculogen TR-2 (6), and 12α-hydroxyverruculogen TR-2 (7), were isolated from terrestrial fungus &lt;i>Penicillium brefeldianum.&lt;/i> All the new compounds were elucidated extensively by the interpretation of their NMR (1D and 2D) spectra and high-resolution mass data, and their absolute configurations were determined by computational chemistry and CD spectra. The absolute configurations of spiro carbon C-2 in spirotryprostatin G (5) and spirotryprostatin C in literature were reported as &lt;i>S&lt;/i>, which were revised to &lt;i>R&lt;/i> based on experimental and calculated CD spectra. All the compounds were evaluated for their antim</pubmed_abstract><journal>Frontiers in microbiology</journal><pagination>1046099</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9702524</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Antibacterial spirooxindole alkaloids from &lt;i>Penicillium brefeldianum&lt;/i> inhibit dimorphism of pathogenic smut fungi.</pubmed_title><pmcid>PMC9702524</pmcid><pubmed_authors>Jiang J</pubmed_authors><pubmed_authors>He F</pubmed_authors><pubmed_authors>Jie L</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Jiang H</pubmed_authors><pubmed_authors>Su Z</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Shi H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Antibacterial spirooxindole alkaloids from &lt;i>Penicillium brefeldianum&lt;/i> inhibit dimorphism of pathogenic smut fungi.</name><description>Three new antibacterial spirooxindole alkaloids, spirobrefeldins A-C (1-3), together with four known analogs, spirotryprostatin M (4), spirotryprostatin G (5), 12β-hydroxyverruculogen TR-2 (6), and 12α-hydroxyverruculogen TR-2 (7), were isolated from terrestrial fungus &lt;i>Penicillium brefeldianum.&lt;/i> All the new compounds were elucidated extensively by the interpretation of their NMR (1D and 2D) spectra and high-resolution mass data, and their absolute configurations were determined by computational chemistry and CD spectra. The absolute configurations of spiro carbon C-2 in spirotryprostatin G (5) and spirotryprostatin C in literature were reported as &lt;i>S&lt;/i>, which were revised to &lt;i>R&lt;/i> based on experimental and calculated CD spectra. All the compounds were evaluated for their antim</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-04T12:02:09.299Z</modification><creation>2025-02-19T03:00:06.176Z</creation></dates><accession>S-EPMC9702524</accession><cross_references><pubmed>36452922</pubmed><doi>10.3389/fmicb.2022.1046099</doi></cross_references></HashMap>