<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ariantari NP</submitter><funding>Deutscher Akademischer Austauschdienst</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Jürgen Manchot Stiftung</funding><pagination>7232-7240</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9049863</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(12)</volume><pubmed_abstract>Didymellanosine (1), the first analogue of the decahydrofluorene-class of natural products bearing a 13-membered macrocyclic alkaloid conjugated with adenosine, and a new benzolactone derivative, ascolactone C (4) along with eight known compounds (2, 3, 5-10), were isolated from a solid rice fermentation of the endophytic fungus &lt;i>Didymella&lt;/i> sp. IEA-3B.1 derived from the host plant &lt;i>Terminalia catappa&lt;/i>. In addition, ascochitamine (11) was obtained when (NH&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>SO&lt;sub>4&lt;/sub> was added to rice medium and is reported here for the first time as a natural product. Didymellanosine (1) displayed strong activity against the murine lymphoma cell line L5178Y, Burkitt's lymphoma B cells (Ramos) and adult lymphoblastic leukemia T cells (Jurkat J16), with IC&lt;sub>50&lt;/sub> v</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Didymellanosine, a new decahydrofluorene analogue, and ascolactone C from &lt;i>Didymella&lt;/i> sp. IEA-3B.1, an endophyte of &lt;i>Terminalia catappa&lt;/i>.</pubmed_title><pmcid>PMC9049863</pmcid><funding_grant_id>270650915/GRK 2158</funding_grant_id><pubmed_authors>Teusch N</pubmed_authors><pubmed_authors>Muller WEG</pubmed_authors><pubmed_authors>Reimche I</pubmed_authors><pubmed_authors>Ariantari NP</pubmed_authors><pubmed_authors>Ancheeva E</pubmed_authors><pubmed_authors>Groner Y</pubmed_authors><pubmed_authors>Meier D</pubmed_authors><pubmed_authors>Liu Z</pubmed_authors><pubmed_authors>Wesselborg S</pubmed_authors><pubmed_authors>Kalscheuer R</pubmed_authors><pubmed_authors>Frank M</pubmed_authors><pubmed_authors>Stuhldreier F</pubmed_authors><pubmed_authors>Proksch P</pubmed_authors></additional><is_claimable>false</is_claimable><name>Didymellanosine, a new decahydrofluorene analogue, and ascolactone C from &lt;i>Didymella&lt;/i> sp. IEA-3B.1, an endophyte of &lt;i>Terminalia catappa&lt;/i>.</name><description>Didymellanosine (1), the first analogue of the decahydrofluorene-class of natural products bearing a 13-membered macrocyclic alkaloid conjugated with adenosine, and a new benzolactone derivative, ascolactone C (4) along with eight known compounds (2, 3, 5-10), were isolated from a solid rice fermentation of the endophytic fungus &lt;i>Didymella&lt;/i> sp. IEA-3B.1 derived from the host plant &lt;i>Terminalia catappa&lt;/i>. In addition, ascochitamine (11) was obtained when (NH&lt;sub>4&lt;/sub>)&lt;sub>2&lt;/sub>SO&lt;sub>4&lt;/sub> was added to rice medium and is reported here for the first time as a natural product. Didymellanosine (1) displayed strong activity against the murine lymphoma cell line L5178Y, Burkitt's lymphoma B cells (Ramos) and adult lymphoblastic leukemia T cells (Jurkat J16), with IC&lt;sub>50&lt;/sub> v</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Feb</publication><modification>2026-05-31T06:06:18.985Z</modification><creation>2025-02-19T01:55:30.119Z</creation></dates><accession>S-EPMC9049863</accession><cross_references><pubmed>35493894</pubmed><doi>10.1039/c9ra10685e</doi></cross_references></HashMap>