<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(6)</volume><submitter>Wang J</submitter><pubmed_abstract>The stimulator of interferon genes (STING), an integral adaptor protein in the DNA-sensing pathway, plays a pivotal role in the innate immune response against infections. Additionally, it presents a valuable therapeutic target for infectious diseases and cancer. We observed that fangchinoline (Fan), a bis-benzylisoquinoline alkaloid (BBA), effectively impedes the replication of vesicular stomatitis virus (VSV), encephalomyocarditis virus (EMCV), influenza A virus (H1N1), and herpes simplex virus-1 (HSV-1) &lt;i>in vitro&lt;/i>. Fan treatment significantly reduced the viral load, attenuated tissue inflammation, and improved survival in a viral sepsis mouse model. Mechanistically, Fan activates the antiviral response in a STING-dependent manner, leading to increased expression of interferon (IFN) </pubmed_abstract><journal>Journal of pharmaceutical analysis</journal><pagination>100972</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11255895</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Fangchinoline induces antiviral response by suppressing STING degradation.</pubmed_title><pmcid>PMC11255895</pmcid><pubmed_authors>Kong L</pubmed_authors><pubmed_authors>Liang X</pubmed_authors><pubmed_authors>Zhang M</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Xie F</pubmed_authors><pubmed_authors>He Y</pubmed_authors><pubmed_authors>Xu A</pubmed_authors><pubmed_authors>Jia X</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Luo T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Fangchinoline induces antiviral response by suppressing STING degradation.</name><description>The stimulator of interferon genes (STING), an integral adaptor protein in the DNA-sensing pathway, plays a pivotal role in the innate immune response against infections. Additionally, it presents a valuable therapeutic target for infectious diseases and cancer. We observed that fangchinoline (Fan), a bis-benzylisoquinoline alkaloid (BBA), effectively impedes the replication of vesicular stomatitis virus (VSV), encephalomyocarditis virus (EMCV), influenza A virus (H1N1), and herpes simplex virus-1 (HSV-1) &lt;i>in vitro&lt;/i>. Fan treatment significantly reduced the viral load, attenuated tissue inflammation, and improved survival in a viral sepsis mouse model. Mechanistically, Fan activates the antiviral response in a STING-dependent manner, leading to increased expression of interferon (IFN) </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-06-01T16:29:35.898Z</modification><creation>2025-04-04T14:46:54.092Z</creation></dates><accession>S-EPMC11255895</accession><cross_references><pubmed>39027910</pubmed><doi>10.1016/j.jpha.2024.100972</doi></cross_references></HashMap>