<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>60</viewCount><searchCount>0</searchCount></scores><additional><submitter>Park SC</submitter><funding>National Research Foundation of Korea</funding><pagination>E176</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6470642</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>17(3)</volume><pubmed_abstract>Six new phenalenone derivatives (1⁻6), along with five known compounds (7⁻11) of the herqueinone class, were isolated from a marine-derived fungus Penicillium sp. The absolute configurations of these compounds were assigned based on chemical modifications and their specific rotations. 4-Hydroxysclerodin (6) and an acetone adduct of a triketone (7) exhibited moderate anti-angiogenetic and anti-inflammatory activities, respectively, while ent-peniciherqueinone (1) and isoherqueinone (9) exhibited moderate abilities to induce adipogenesis without cytotoxicity.</pubmed_abstract><journal>Marine drugs</journal><pubmed_title>Phenalenones from a Marine-Derived Fungus Penicillium Sp.</pubmed_title><pmcid>PMC6470642</pmcid><funding_grant_id>2018R1A4A1021703</funding_grant_id><pubmed_authors>Kim D</pubmed_authors><pubmed_authors>Lee SK</pubmed_authors><pubmed_authors>Park SC</pubmed_authors><pubmed_authors>Julianti E</pubmed_authors><pubmed_authors>Oh KB</pubmed_authors><pubmed_authors>Shin AJ</pubmed_authors><pubmed_authors>Noh M</pubmed_authors><pubmed_authors>Ahn S</pubmed_authors><pubmed_authors>Oh DC</pubmed_authors><view_count>60</view_count></additional><is_claimable>false</is_claimable><name>Phenalenones from a Marine-Derived Fungus Penicillium Sp.</name><description>Six new phenalenone derivatives (1⁻6), along with five known compounds (7⁻11) of the herqueinone class, were isolated from a marine-derived fungus Penicillium sp. The absolute configurations of these compounds were assigned based on chemical modifications and their specific rotations. 4-Hydroxysclerodin (6) and an acetone adduct of a triketone (7) exhibited moderate anti-angiogenetic and anti-inflammatory activities, respectively, while ent-peniciherqueinone (1) and isoherqueinone (9) exhibited moderate abilities to induce adipogenesis without cytotoxicity.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Mar</publication><modification>2024-11-15T02:45:43.852Z</modification><creation>2019-06-06T22:57:14Z</creation></dates><accession>S-EPMC6470642</accession><cross_references><pubmed>30889916</pubmed><doi>10.3390/md17030176</doi></cross_references></HashMap>