<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17</volume><submitter>Yang WG</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Artemisinin (ART) is a safe and effective antimalarial drug. In recent years, antimalarial drugs have demonstrated a good therapeutic efficacy in IgA nephropathy, suggesting that this may become a new treatment option.&lt;h4>Purpose&lt;/h4>We aimed to evaluate the effect and mechanism of artemisinin in IgA nephropathy.&lt;h4>Methods&lt;/h4>In this study, CMap database was used to predict the artemisinin therapeutic effect for IgA nephropathy. A network pharmacology approach was applied to explore the unknown mechanism of artemisinin in IgA nephropathy. We used molecular docking to predict the binding affinity of artemisinin with the targets. A mouse model of IgA nephropathy was established to investigate the therapeutic effect of artemisinin on IgA nephropathy. In vitro, the cell co</pubmed_abstract><journal>Drug design, development and therapy</journal><pagination>1679-1697</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10257916</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exploration of Artemisinin Against IgA Nephropathy via AKT/Nrf2 Pathway by Bioinformatics and Experimental Validation.</pubmed_title><pmcid>PMC10257916</pmcid><pubmed_authors>Yang WG</pubmed_authors><pubmed_authors>He WJ</pubmed_authors><pubmed_authors>Sun A</pubmed_authors><pubmed_authors>Liu LL</pubmed_authors><pubmed_authors>Liu N</pubmed_authors><pubmed_authors>Zhu R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exploration of Artemisinin Against IgA Nephropathy via AKT/Nrf2 Pathway by Bioinformatics and Experimental Validation.</name><description>&lt;h4>Background&lt;/h4>Artemisinin (ART) is a safe and effective antimalarial drug. In recent years, antimalarial drugs have demonstrated a good therapeutic efficacy in IgA nephropathy, suggesting that this may become a new treatment option.&lt;h4>Purpose&lt;/h4>We aimed to evaluate the effect and mechanism of artemisinin in IgA nephropathy.&lt;h4>Methods&lt;/h4>In this study, CMap database was used to predict the artemisinin therapeutic effect for IgA nephropathy. A network pharmacology approach was applied to explore the unknown mechanism of artemisinin in IgA nephropathy. We used molecular docking to predict the binding affinity of artemisinin with the targets. A mouse model of IgA nephropathy was established to investigate the therapeutic effect of artemisinin on IgA nephropathy. In vitro, the cell co</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023</publication><modification>2025-04-04T10:21:21.932Z</modification><creation>2025-02-19T02:37:56.818Z</creation></dates><accession>S-EPMC10257916</accession><cross_references><pubmed>37309415</pubmed><doi>10.2147/DDDT.S403422</doi></cross_references></HashMap>