<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Rivera-Chavez J</submitter><funding>NCCIH NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><pagination>594-597</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6785197</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>60(8)</volume><pubmed_abstract>A new 8,8'-binaphthopyranone (mycopyranone, &lt;b>1&lt;/b>) was isolated from a solid fermentation of &lt;i>Phialemoniopsis&lt;/i> sp. (fungal strain MSX61662), and the structure was elucidated via analysis of the NMR and HRESIMS data. The axial chirality of &lt;b>1&lt;/b> was determined to be &lt;i>M&lt;/i> by ECD. The central chirality at C-4/C-4' was assigned through a modified Mosher's method, while the absolute configuration at C-3/C-3' was deduced based on analysis of the &lt;sup>3&lt;/sup> &lt;i>J&lt;/i> &lt;sub>H-3-H-4&lt;/sub> values and NOESY correlations. Compound &lt;b>1&lt;/b> was evaluated for its antimicrobial properties against &lt;i>Staphylococcus aureus&lt;/i> SA1199 and a clinically relevant methicillin-resistant &lt;i>S. aureus&lt;/i> strain (MRSA USA300 LAC strain AH1263). Compound &lt;b>1&lt;/b> inhibited the growth of both strains </pubmed_abstract><journal>Tetrahedron letters</journal><pubmed_title>Mycopyranone: a 8,8'-binaphthopyranone with potent anti-MRSA activity from the fungus &lt;i>Phialemoniopsis&lt;/i> sp.</pubmed_title><pmcid>PMC6785197</pmcid><funding_grant_id>P01 CA125066</funding_grant_id><funding_grant_id>T32 AT008938</funding_grant_id><pubmed_authors>Cech NB</pubmed_authors><pubmed_authors>Pearce CJ</pubmed_authors><pubmed_authors>Garcia-Salazar JJ</pubmed_authors><pubmed_authors>Raja HA</pubmed_authors><pubmed_authors>Oberlies NH</pubmed_authors><pubmed_authors>Rivera-Chavez J</pubmed_authors><pubmed_authors>Caesar L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mycopyranone: a 8,8'-binaphthopyranone with potent anti-MRSA activity from the fungus &lt;i>Phialemoniopsis&lt;/i> sp.</name><description>A new 8,8'-binaphthopyranone (mycopyranone, &lt;b>1&lt;/b>) was isolated from a solid fermentation of &lt;i>Phialemoniopsis&lt;/i> sp. (fungal strain MSX61662), and the structure was elucidated via analysis of the NMR and HRESIMS data. The axial chirality of &lt;b>1&lt;/b> was determined to be &lt;i>M&lt;/i> by ECD. The central chirality at C-4/C-4' was assigned through a modified Mosher's method, while the absolute configuration at C-3/C-3' was deduced based on analysis of the &lt;sup>3&lt;/sup> &lt;i>J&lt;/i> &lt;sub>H-3-H-4&lt;/sub> values and NOESY correlations. Compound &lt;b>1&lt;/b> was evaluated for its antimicrobial properties against &lt;i>Staphylococcus aureus&lt;/i> SA1199 and a clinically relevant methicillin-resistant &lt;i>S. aureus&lt;/i> strain (MRSA USA300 LAC strain AH1263). Compound &lt;b>1&lt;/b> inhibited the growth of both strains </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Feb</publication><modification>2026-04-29T03:43:44.854Z</modification><creation>2020-05-22T10:35:48Z</creation></dates><accession>S-EPMC6785197</accession><cross_references><pubmed>31598014</pubmed><doi>10.1016/j.tetlet.2019.01.029</doi></cross_references></HashMap>