<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>13</volume><submitter>Su J</submitter><pubmed_abstract>Three chalcone derivatives, abelmanihotols A-C &lt;b>(1-3)&lt;/b>, and nine known compounds were isolated from &lt;i>A. manihot&lt;/i> seeds, and their structures were determined using HRESIMS and NMR spectroscopic analysis. Compound &lt;b>1&lt;/b> exhibited the most potent inhibitory effect (IC&lt;sub>50&lt;/sub> = 4.79 ± 0.72 μM) against lipopolysaccharide (LPS)-induced NO release in THP-1 cells, and &lt;b>s&lt;/b>ignificantly inhibited interleukin 1β (IL-1β) secretion, which is stimulated by LPS plus nigericin (IC&lt;sub>50&lt;/sub> = 11.86 ± 1.20 μM), ATP or MSU, in THP-1 cells. A preliminary mechanism of action study indicated that compound &lt;b>1&lt;/b> blocked the formation of nucleotide oligomerization domain-like receptor protein-3 (NLRP3) inflammasome formation by suppressing apoptosis-associated speck-like protein olig</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>932198</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9301202</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Chalcone Derivatives From &lt;i>Abelmoschus manihot&lt;/i> Seeds Restrain NLRP3 Inflammasome Assembly by Inhibiting ASC Oligomerization.</pubmed_title><pmcid>PMC9301202</pmcid><pubmed_authors>Kang X</pubmed_authors><pubmed_authors>Liu J</pubmed_authors><pubmed_authors>Tao Y</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Diao Q</pubmed_authors><pubmed_authors>Su J</pubmed_authors><pubmed_authors>Liu D</pubmed_authors><pubmed_authors>Yang F</pubmed_authors><pubmed_authors>Meng X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Chalcone Derivatives From &lt;i>Abelmoschus manihot&lt;/i> Seeds Restrain NLRP3 Inflammasome Assembly by Inhibiting ASC Oligomerization.</name><description>Three chalcone derivatives, abelmanihotols A-C &lt;b>(1-3)&lt;/b>, and nine known compounds were isolated from &lt;i>A. manihot&lt;/i> seeds, and their structures were determined using HRESIMS and NMR spectroscopic analysis. Compound &lt;b>1&lt;/b> exhibited the most potent inhibitory effect (IC&lt;sub>50&lt;/sub> = 4.79 ± 0.72 μM) against lipopolysaccharide (LPS)-induced NO release in THP-1 cells, and &lt;b>s&lt;/b>ignificantly inhibited interleukin 1β (IL-1β) secretion, which is stimulated by LPS plus nigericin (IC&lt;sub>50&lt;/sub> = 11.86 ± 1.20 μM), ATP or MSU, in THP-1 cells. A preliminary mechanism of action study indicated that compound &lt;b>1&lt;/b> blocked the formation of nucleotide oligomerization domain-like receptor protein-3 (NLRP3) inflammasome formation by suppressing apoptosis-associated speck-like protein olig</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022</publication><modification>2025-04-05T11:51:24.882Z</modification><creation>2025-04-05T11:51:24.882Z</creation></dates><accession>S-EPMC9301202</accession><cross_references><pubmed>35873581</pubmed><doi>10.3389/fphar.2022.932198</doi></cross_references></HashMap>