<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fayez S</submitter><funding>Deutscher Akademischer Austauschdienst, DAAD</funding><funding>Deutsche Forschungsgemeinschaft</funding><pagination>15738-15748</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9064271</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(28)</volume><pubmed_abstract>A unique series of six biaryl natural products displaying four different coupling types (5,1', 7,1', 7,8', and 5,8') were isolated from the roots of the West African liana &lt;i>Ancistrocladus abbreviatus&lt;/i> (Ancistrocladaceae). Although at first sight structurally diverse, these secondary metabolites all have in common that they belong to the rare group of naphthylisoquinoline alkaloids with a fully dehydrogenated isoquinoline portion. Among the African &lt;i>Ancistrocladus&lt;/i> species, &lt;i>A. abbreviatus&lt;/i> is so far only the second one that was found to produce compounds with such a molecular entity. Here, we report on four new representatives, named ancistrobreveines A-D (12-14, and 6). They were identified along with the two known alkaloids 6-&lt;i>O&lt;/i>-methylhamateine (4) and &lt;i>ent&lt;/i>-dio</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Ancistrobreveines A-D and related dehydrogenated naphthylisoquinoline alkaloids with antiproliferative activities against leukemia cells, from the West African liana &lt;i>Ancistrocladus abbreviatus&lt;/i>.</pubmed_title><pmcid>PMC9064271</pmcid><funding_grant_id>to Shaimaa Fayez</funding_grant_id><funding_grant_id>SFB 630</funding_grant_id><funding_grant_id>Br699/14-2</funding_grant_id><pubmed_authors>Efferth T</pubmed_authors><pubmed_authors>Bringmann G</pubmed_authors><pubmed_authors>Fayez S</pubmed_authors><pubmed_authors>Assi LA</pubmed_authors><pubmed_authors>Seo EJ</pubmed_authors><pubmed_authors>Feineis D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ancistrobreveines A-D and related dehydrogenated naphthylisoquinoline alkaloids with antiproliferative activities against leukemia cells, from the West African liana &lt;i>Ancistrocladus abbreviatus&lt;/i>.</name><description>A unique series of six biaryl natural products displaying four different coupling types (5,1', 7,1', 7,8', and 5,8') were isolated from the roots of the West African liana &lt;i>Ancistrocladus abbreviatus&lt;/i> (Ancistrocladaceae). Although at first sight structurally diverse, these secondary metabolites all have in common that they belong to the rare group of naphthylisoquinoline alkaloids with a fully dehydrogenated isoquinoline portion. Among the African &lt;i>Ancistrocladus&lt;/i> species, &lt;i>A. abbreviatus&lt;/i> is so far only the second one that was found to produce compounds with such a molecular entity. Here, we report on four new representatives, named ancistrobreveines A-D (12-14, and 6). They were identified along with the two known alkaloids 6-&lt;i>O&lt;/i>-methylhamateine (4) and &lt;i>ent&lt;/i>-dio</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May</publication><modification>2025-04-04T12:43:31.018Z</modification><creation>2025-04-04T12:43:31.018Z</creation></dates><accession>S-EPMC9064271</accession><cross_references><pubmed>35521375</pubmed><doi>10.1039/c9ra03105g</doi></cross_references></HashMap>