<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Djoumessi AK</submitter><funding>German Academic Exchange Service</funding><funding>Alango Foundation</funding><pagination>298</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9966138</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(2)</volume><pubmed_abstract>The chemical investigation of the EtOH extract from the stem bark of &lt;i>Trichilia monadelpha&lt;/i> (Thonn.) J. J. De Wilde afforded two new limonoids (&lt;b>1&lt;/b> and &lt;b>2&lt;/b>): 24-acetoxy-21,25-dihydroxy-21,23-epoxytirucall-7-en-3-one (&lt;b>1&lt;/b>) and (6&lt;i>R&lt;/i>)-1-&lt;i>O&lt;/i>-deacetylkhayanolide E (&lt;b>2&lt;/b>), together with eleven known compounds (&lt;b>3&lt;/b>-&lt;b>13&lt;/b>), including additional limonoids, flavonoids, triterpenoids, steroids, and fatty acid. Their structures were determined using 1D- and 2D-NMR experiments, ESI mass spectrometry, and single crystal X-ray diffraction analysis. The antibacterial and antiplasmodial activities of the extracts, sub-extracts, fractions, and some of the isolated compounds were evaluated in known pathogenic strains, including &lt;i>Staphylococcus aureus&lt;/i> and &lt;i>P</pubmed_abstract><journal>Metabolites</journal><pubmed_title>Constituents of the Stem Bark of &lt;i>Trichilia monadelpha&lt;/i> (Thonn.) J. J. De Wilde (Meliaceae) and Their Antibacterial and Antiplasmodial Activities.</pubmed_title><pmcid>PMC9966138</pmcid><funding_grant_id>57316173</funding_grant_id><funding_grant_id>Reference Hospital of African Medicine</funding_grant_id><pubmed_authors>Neumann B</pubmed_authors><pubmed_authors>Chouna JR</pubmed_authors><pubmed_authors>Ayong L</pubmed_authors><pubmed_authors>Sewald N</pubmed_authors><pubmed_authors>Efange NM</pubmed_authors><pubmed_authors>Stammler HG</pubmed_authors><pubmed_authors>Bitchagno GTM</pubmed_authors><pubmed_authors>Lenta BN</pubmed_authors><pubmed_authors>Nkenfou CN</pubmed_authors><pubmed_authors>Nkeng-Efouet-Alango P</pubmed_authors><pubmed_authors>Nono RN</pubmed_authors><pubmed_authors>Djoumessi AK</pubmed_authors></additional><is_claimable>false</is_claimable><name>Constituents of the Stem Bark of &lt;i>Trichilia monadelpha&lt;/i> (Thonn.) J. J. De Wilde (Meliaceae) and Their Antibacterial and Antiplasmodial Activities.</name><description>The chemical investigation of the EtOH extract from the stem bark of &lt;i>Trichilia monadelpha&lt;/i> (Thonn.) J. J. De Wilde afforded two new limonoids (&lt;b>1&lt;/b> and &lt;b>2&lt;/b>): 24-acetoxy-21,25-dihydroxy-21,23-epoxytirucall-7-en-3-one (&lt;b>1&lt;/b>) and (6&lt;i>R&lt;/i>)-1-&lt;i>O&lt;/i>-deacetylkhayanolide E (&lt;b>2&lt;/b>), together with eleven known compounds (&lt;b>3&lt;/b>-&lt;b>13&lt;/b>), including additional limonoids, flavonoids, triterpenoids, steroids, and fatty acid. Their structures were determined using 1D- and 2D-NMR experiments, ESI mass spectrometry, and single crystal X-ray diffraction analysis. The antibacterial and antiplasmodial activities of the extracts, sub-extracts, fractions, and some of the isolated compounds were evaluated in known pathogenic strains, including &lt;i>Staphylococcus aureus&lt;/i> and &lt;i>P</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-26T00:05:04.272Z</modification><creation>2025-02-18T23:57:44.861Z</creation></dates><accession>S-EPMC9966138</accession><cross_references><pubmed>36837917</pubmed><doi>10.3390/metabo13020298</doi></cross_references></HashMap>