<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Tian Y</submitter><funding>Sheng Yin</funding><funding>Rong Pu</funding><funding>Guihua Tang</funding><pagination>511</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9867043</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>28(2)</volume><pubmed_abstract>Glochidpurnoids A and B (&lt;b>1&lt;/b> and &lt;b>2&lt;/b>), two new coumaroyl or feruloyl oleananes, along with 17 known triterpenoids (&lt;b>3&lt;/b>-&lt;b>19&lt;/b>) were obtained from the stems and twigs of &lt;i>Glochidion puberum&lt;/i>. Their structures were elucidated by extensive spectroscopic data analyses, chemical methods, and single crystal X-ray diffraction. All compounds were screened for cytotoxicity against the colorectal cancer cell line HCT-116, and &lt;b>2&lt;/b>, &lt;b>3&lt;/b>, &lt;b>5&lt;/b>, &lt;b>6&lt;/b>, &lt;b>11&lt;/b>, and &lt;b>17&lt;/b> showed remarkable inhibitory activities (IC&lt;sub>50&lt;/sub>: 0.80-2.99 μM), being more active than the positive control 5-fluorouracil (5-FU). The mechanistic study of &lt;b>2&lt;/b>, the most potent compound, showed that it could induce endoplasmic reticulum (ER) stress-mediated apoptosis and improv</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Glochodpurnoid B from &lt;i>Glochidion puberum&lt;/i> Induces Endoplasmic Reticulum Stress-Mediated Apoptosis in Colorectal Cancer Cells.</pubmed_title><pmcid>PMC9867043</pmcid><funding_grant_id>2021B1515140062</funding_grant_id><funding_grant_id>82273804</funding_grant_id><funding_grant_id>81973195</funding_grant_id><funding_grant_id>SML2021SP301</funding_grant_id><funding_grant_id>SZBL2021080601007</funding_grant_id><funding_grant_id>81973203</funding_grant_id><pubmed_authors>Pu R</pubmed_authors><pubmed_authors>Yuan F</pubmed_authors><pubmed_authors>Huang D</pubmed_authors><pubmed_authors>Huang Y</pubmed_authors><pubmed_authors>Yin S</pubmed_authors><pubmed_authors>Tian Y</pubmed_authors><pubmed_authors>Yin A</pubmed_authors><pubmed_authors>Tang G</pubmed_authors><pubmed_authors>Fan R</pubmed_authors><pubmed_authors>Yin Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glochodpurnoid B from &lt;i>Glochidion puberum&lt;/i> Induces Endoplasmic Reticulum Stress-Mediated Apoptosis in Colorectal Cancer Cells.</name><description>Glochidpurnoids A and B (&lt;b>1&lt;/b> and &lt;b>2&lt;/b>), two new coumaroyl or feruloyl oleananes, along with 17 known triterpenoids (&lt;b>3&lt;/b>-&lt;b>19&lt;/b>) were obtained from the stems and twigs of &lt;i>Glochidion puberum&lt;/i>. Their structures were elucidated by extensive spectroscopic data analyses, chemical methods, and single crystal X-ray diffraction. All compounds were screened for cytotoxicity against the colorectal cancer cell line HCT-116, and &lt;b>2&lt;/b>, &lt;b>3&lt;/b>, &lt;b>5&lt;/b>, &lt;b>6&lt;/b>, &lt;b>11&lt;/b>, and &lt;b>17&lt;/b> showed remarkable inhibitory activities (IC&lt;sub>50&lt;/sub>: 0.80-2.99 μM), being more active than the positive control 5-fluorouracil (5-FU). The mechanistic study of &lt;b>2&lt;/b>, the most potent compound, showed that it could induce endoplasmic reticulum (ER) stress-mediated apoptosis and improv</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-04-26T00:36:51.623Z</modification><creation>2025-02-19T03:00:18.283Z</creation></dates><accession>S-EPMC9867043</accession><cross_references><pubmed>36677570</pubmed><doi>10.3390/molecules28020511</doi></cross_references></HashMap>