<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chang FP</submitter><funding>Chinese Medicine Research Center, China Medical University</funding><funding>Taiwan Ministry of Health and Welfare Clinical Trial Center</funding><pagination>E4271</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6930649</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>24(23)</volume><pubmed_abstract>One new iridoid, namely neonanin C (&lt;b>1&lt;/b>) one monocyclic iridoid ring-opened derivative namely neonanin D &lt;b>(2)&lt;/b>, two new bis-iridoid derivatives namely reticunin A (&lt;b>3&lt;/b>) and reticunin B (&lt;b>4&lt;/b>) with sixteen known compounds (&lt;b>5&lt;/b>-&lt;b>20&lt;/b>) were isolated from the stems of &lt;i>Neonauclea reticulata&lt;/i> (Havil.) Merr. These new structures were determined by the detailed analysis of spectroscopic data and comparison with the data of known analogues. Compounds &lt;b>1&lt;/b>-&lt;b>20&lt;/b> were evaluated for inhibition of nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages cell line. The results showed that all compounds exhibited no obvious cytotoxicity compared to the control group and five compounds including isoboonein (&lt;b>7&lt;/b>), syringaresinol (&lt;b>10&lt;/b>), (+)-medioresinol (&lt;b>12&lt;/b>), protocatechuic acid (&lt;b>14&lt;/b>) and &lt;i>trans&lt;/i>-caffeic acid (&lt;b>15&lt;/b>) exhibited inhibitory activities with IC&lt;sub>50&lt;/sub> values at 86.27 ± 3.45; 9.18 ± 1.90; 76.18 ± 2.42; 72.91 ± 4.97 and 95.16 ± 1.20 µg/mL, respectively.</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Four New Iridoid Metabolites Have Been Isolated from the Stems of &lt;i>Neonauclea reticulata&lt;/i> (Havil.) Merr. with Anti-Inflammatory Activities on LPS-Induced RAW264.7 Cells.</pubmed_title><pmcid>PMC6930649</pmcid><funding_grant_id>CMRC-CHM-4</funding_grant_id><funding_grant_id>MOHW108-TDU-B-212-133004</funding_grant_id><pubmed_authors>Huang SS</pubmed_authors><pubmed_authors>Kuo TF</pubmed_authors><pubmed_authors>Kuo YH</pubmed_authors><pubmed_authors>Lee TH</pubmed_authors><pubmed_authors>Huang GJ</pubmed_authors><pubmed_authors>Chang CI</pubmed_authors><pubmed_authors>Chang FP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Four New Iridoid Metabolites Have Been Isolated from the Stems of &lt;i>Neonauclea reticulata&lt;/i> (Havil.) Merr. with Anti-Inflammatory Activities on LPS-Induced RAW264.7 Cells.</name><description>One new iridoid, namely neonanin C (&lt;b>1&lt;/b>) one monocyclic iridoid ring-opened derivative namely neonanin D &lt;b>(2)&lt;/b>, two new bis-iridoid derivatives namely reticunin A (&lt;b>3&lt;/b>) and reticunin B (&lt;b>4&lt;/b>) with sixteen known compounds (&lt;b>5&lt;/b>-&lt;b>20&lt;/b>) were isolated from the stems of &lt;i>Neonauclea reticulata&lt;/i> (Havil.) Merr. These new structures were determined by the detailed analysis of spectroscopic data and comparison with the data of known analogues. Compounds &lt;b>1&lt;/b>-&lt;b>20&lt;/b> were evaluated for inhibition of nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages cell line. The results showed that all compounds exhibited no obvious cytotoxicity compared to the control group and five compounds including isoboonein (&lt;b>7&lt;/b>), syringaresinol (&lt;b>10&lt;/b>), (+)-medioresinol (&lt;b>12&lt;/b>), protocatechuic acid (&lt;b>14&lt;/b>) and &lt;i>trans&lt;/i>-caffeic acid (&lt;b>15&lt;/b>) exhibited inhibitory activities with IC&lt;sub>50&lt;/sub> values at 86.27 ± 3.45; 9.18 ± 1.90; 76.18 ± 2.42; 72.91 ± 4.97 and 95.16 ± 1.20 µg/mL, respectively.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Nov</publication><modification>2025-04-05T16:21:19.542Z</modification><creation>2020-05-22T00:46:23Z</creation></dates><accession>S-EPMC6930649</accession><cross_references><pubmed>31771186</pubmed><doi>10.3390/molecules24234271</doi></cross_references></HashMap>