<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>88(10)</volume><submitter>Lopez-Sampedro E</submitter><pubmed_abstract>Sea cucumbers (Holothuriidae) are highly valued in traditional medicine and are recognized for their diverse bioactivities, which are largely attributed to their rich triterpene glycoside content. Given that &lt;i>Holothuria inornata&lt;/i> was chemically uncharacterized, this study describes the bioassay-guided isolation of these compounds. Nine sulfated saponins were purified, and their structures were elucidated using UPLC-QTOF/HR-ESI-MS&lt;sup>&lt;i>n&lt;/i>&lt;/sup> and comprehensive NMR spectroscopy. Six new compounds were identified, including inornatosides A-C (&lt;b>1&lt;/b>-&lt;b>3&lt;/b>) and 22&lt;i>R&lt;/i>-holothurin B (&lt;b>6&lt;/b>), all possessing a holostane-type aglycone, alongside inornatosides D (&lt;b>4&lt;/b>) and E (&lt;b>5&lt;/b>), which feature unique aglycones. Cytotoxic assays revealed that inornatoside B (&lt;b>2&lt;/b</pubmed_abstract><journal>Journal of natural products</journal><pagination>2372-2382</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12560079</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Cytotoxic Triterpene Glycosides from Mexican Sea Cucumber &amp;lt;i&amp;gt;Holothuria inornata&amp;lt;/i&amp;gt;.</pubmed_title><pmcid>PMC12560079</pmcid><pubmed_authors>Lopez-Sampedro E</pubmed_authors><pubmed_authors>Arreguin-Espinosa R</pubmed_authors><pubmed_authors>Simonet AM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Cytotoxic Triterpene Glycosides from Mexican Sea Cucumber &amp;lt;i&amp;gt;Holothuria inornata&amp;lt;/i&amp;gt;.</name><description>Sea cucumbers (Holothuriidae) are highly valued in traditional medicine and are recognized for their diverse bioactivities, which are largely attributed to their rich triterpene glycoside content. Given that &lt;i>Holothuria inornata&lt;/i> was chemically uncharacterized, this study describes the bioassay-guided isolation of these compounds. Nine sulfated saponins were purified, and their structures were elucidated using UPLC-QTOF/HR-ESI-MS&lt;sup>&lt;i>n&lt;/i>&lt;/sup> and comprehensive NMR spectroscopy. Six new compounds were identified, including inornatosides A-C (&lt;b>1&lt;/b>-&lt;b>3&lt;/b>) and 22&lt;i>R&lt;/i>-holothurin B (&lt;b>6&lt;/b>), all possessing a holostane-type aglycone, alongside inornatosides D (&lt;b>4&lt;/b>) and E (&lt;b>5&lt;/b>), which feature unique aglycones. Cytotoxic assays revealed that inornatoside B (&lt;b>2&lt;/b</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-05T08:49:48.391Z</modification><creation>2026-05-14T03:12:33.772Z</creation></dates><accession>S-EPMC12560079</accession><cross_references><pubmed>40976948</pubmed><doi>10.1021/acs.jnatprod.5c00716</doi></cross_references></HashMap>