<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Wang F</submitter><funding>ANPCyT</funding><funding>Secretar?a de Ciencia y T?cnica, Universidad Nacional de R?o Cuarto</funding><funding>Hawaii Community Foundation</funding><funding>NIH</funding><funding>NIGMS NIH HHS</funding><pagination>4408-4412</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8904076</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>22(11)</volume><pubmed_abstract>Waikikiamides A-C (&lt;b>1&lt;/b>-&lt;b>3&lt;/b>), structurally complex diketopiperazine derivatives, and putative biogenic precursors, (+)-semivioxanthin (&lt;b>4&lt;/b>), notoamide F (&lt;b>5&lt;/b>), and (-)-notoamide A (&lt;b>6&lt;/b>), were isolated from &lt;i>Aspergillus&lt;/i> sp. FM242. &lt;b>1&lt;/b> and &lt;b>2&lt;/b>, bearing a hendecacyclic ring system, represent a novel skeleton. &lt;b>3&lt;/b> features the first unique heterodimer of two notoamide analogs with an N-O-C bridge. Compounds &lt;b>1&lt;/b> and &lt;b>3&lt;/b> exhibit antiproliferative activity with IC&lt;sub>50&lt;/sub> values in the range of 0.56 to 1.86 μM. The gene clusters mined from the sequenced genome support their putative biosynthetic pathways.</pubmed_abstract><journal>Organic letters</journal><pubmed_title>Waikikiamides A-C: Complex Diketopiperazine Dimer and Diketopiperazine-Polyketide Hybrids from a Hawaiian Marine Fungal Strain &lt;i>Aspergillus&lt;/i> sp. FM242.</pubmed_title><pmcid>PMC8904076</pmcid><funding_grant_id>15ADVC-74420</funding_grant_id><funding_grant_id>R35 GM128742</funding_grant_id><funding_grant_id>P20 GM103466</funding_grant_id><funding_grant_id>17CON- 86295</funding_grant_id><funding_grant_id>PICT-2016-0116</funding_grant_id><funding_grant_id>5P20GM103466</funding_grant_id><funding_grant_id>BIO 500</funding_grant_id><funding_grant_id>1R35GM128742</funding_grant_id><pubmed_authors>Zheng SL</pubmed_authors><pubmed_authors>Sarotti AM</pubmed_authors><pubmed_authors>Ding Y</pubmed_authors><pubmed_authors>Li C</pubmed_authors><pubmed_authors>Jiang G</pubmed_authors><pubmed_authors>Huguet-Tapia JC</pubmed_authors><pubmed_authors>Wang F</pubmed_authors><pubmed_authors>Cao S</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Waikikiamides A-C: Complex Diketopiperazine Dimer and Diketopiperazine-Polyketide Hybrids from a Hawaiian Marine Fungal Strain &lt;i>Aspergillus&lt;/i> sp. FM242.</name><description>Waikikiamides A-C (&lt;b>1&lt;/b>-&lt;b>3&lt;/b>), structurally complex diketopiperazine derivatives, and putative biogenic precursors, (+)-semivioxanthin (&lt;b>4&lt;/b>), notoamide F (&lt;b>5&lt;/b>), and (-)-notoamide A (&lt;b>6&lt;/b>), were isolated from &lt;i>Aspergillus&lt;/i> sp. FM242. &lt;b>1&lt;/b> and &lt;b>2&lt;/b>, bearing a hendecacyclic ring system, represent a novel skeleton. &lt;b>3&lt;/b> features the first unique heterodimer of two notoamide analogs with an N-O-C bridge. Compounds &lt;b>1&lt;/b> and &lt;b>3&lt;/b> exhibit antiproliferative activity with IC&lt;sub>50&lt;/sub> values in the range of 0.56 to 1.86 μM. The gene clusters mined from the sequenced genome support their putative biosynthetic pathways.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jun</publication><modification>2026-06-01T02:34:50.554Z</modification><creation>2024-10-16T15:02:21.022Z</creation></dates><accession>S-EPMC8904076</accession><cross_references><pubmed>32433885</pubmed><doi>10.1021/acs.orglett.0c01411</doi></cross_references></HashMap>