<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang PP</submitter><funding>National Key R&amp;amp;D Program of China</funding><funding>National Key R&amp;D Program of China</funding><funding>National New Drug Innovation Major Project</funding><funding>National Natural Science Foundation of China</funding><pagination>81-86</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7933302</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(1)</volume><pubmed_abstract>Four new limonoids, toonayunnanaes F - I (1 - 4), and six known compounds (5 - 10) were isolated from the barks of Toona ciliata. Their structures were elucidated by thoroughly analyzing of NMR and HRMS data, and single-crystal X-ray diffraction of 1. The oxetane ring moiety in 1 was rare in limonoids and other natural products. Compound 1 showed nitric oxide (NO) inhibitory effect with an IC&lt;sub>50&lt;/sub> 38.45 ± 0.41 µM in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages.</pubmed_abstract><journal>Natural products and bioprospecting</journal><pubmed_title>Four New Limonoids from the Barks of Toona ciliata.</pubmed_title><pmcid>PMC7933302</pmcid><funding_grant_id>2018YFC1707105</funding_grant_id><funding_grant_id>31470416</funding_grant_id><funding_grant_id>2018ZX09711-001-007</funding_grant_id><pubmed_authors>Zhang PP</pubmed_authors><pubmed_authors>Cui ZR</pubmed_authors><pubmed_authors>Xue S</pubmed_authors><pubmed_authors>Luo J</pubmed_authors><pubmed_authors>Kong LY</pubmed_authors><pubmed_authors>Bu YG</pubmed_authors><pubmed_authors>Tang PF</pubmed_authors></additional><is_claimable>false</is_claimable><name>Four New Limonoids from the Barks of Toona ciliata.</name><description>Four new limonoids, toonayunnanaes F - I (1 - 4), and six known compounds (5 - 10) were isolated from the barks of Toona ciliata. Their structures were elucidated by thoroughly analyzing of NMR and HRMS data, and single-crystal X-ray diffraction of 1. The oxetane ring moiety in 1 was rare in limonoids and other natural products. Compound 1 showed nitric oxide (NO) inhibitory effect with an IC&lt;sub>50&lt;/sub> 38.45 ± 0.41 µM in lipopolysaccharide (LPS)-activated RAW 264.7 macrophages.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Feb</publication><modification>2025-04-22T08:20:06.82Z</modification><creation>2025-04-05T22:29:45.709Z</creation></dates><accession>S-EPMC7933302</accession><cross_references><pubmed>33098068</pubmed><doi>10.1007/s13659-020-00274-w</doi></cross_references></HashMap>