<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chu Y</submitter><funding>Clinical Technology Development Foundation of Jiangsu University</funding><funding>Jiangsu Government Scholarship for Overseas Studies</funding><funding>Foundation of the Science and Technology Project of Wujin</funding><funding>Foundation of the Youth Science and Technology Project of Changzhou Health and Family Planning Commission</funding><funding>Changzhou High-Level Medical Talents Training Project</funding><funding>Special Fund for Clinical Medicine of Jiangsu University</funding><funding>Innovative and Entrepreneurial Plan of Jiangsu Province</funding><pagination>227</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7388529</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>20(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Wogonin, a natural flavonoid-like chemical compound, exhibits anti-inflammatory, antitumor, antiviral, neuroprotective, and anxiolytic effects by modulating a variety of cellular signaling pathways including PI3K-Akt, p53, nuclear factor κB (NF-κB), mitogen-activated protein kinase (MAPK) pathways. In this study, its antiviral effect against herpes simplex virus (HSV) type 1 and 2 (HSV-1 and HSV-2) replication was investigated.&lt;h4>Results&lt;/h4>Wogonin suppressed HSV-2-induced cytopathic effect (CPE) and reduced viral mRNA transcription, viral protein synthesis, and infectious virion particle titers in a dose-dependent manner. A time-of-drug-addition assay demonstrated that wogonin acted as a postentry viral inhibitor. Wogonin also significantly reduced HSV-induced NF-κB a</pubmed_abstract><journal>BMC microbiology</journal><pubmed_title>Wogonin inhibits in vitro herpes simplex virus type 1 and 2 infection by modulating cellular NF-κB and MAPK pathways.</pubmed_title><pmcid>PMC7388529</pmcid><funding_grant_id>WS201402</funding_grant_id><funding_grant_id>WS201710</funding_grant_id><funding_grant_id>QN201505</funding_grant_id><funding_grant_id>JDLC2X020</funding_grant_id><funding_grant_id>JLY20160038</funding_grant_id><funding_grant_id>2016CZBJ060</funding_grant_id><pubmed_authors>Xu L</pubmed_authors><pubmed_authors>Yun Z</pubmed_authors><pubmed_authors>Wu Z</pubmed_authors><pubmed_authors>Su A</pubmed_authors><pubmed_authors>Lv X</pubmed_authors><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Chu Y</pubmed_authors><pubmed_authors>Song S</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Chen D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Wogonin inhibits in vitro herpes simplex virus type 1 and 2 infection by modulating cellular NF-κB and MAPK pathways.</name><description>&lt;h4>Background&lt;/h4>Wogonin, a natural flavonoid-like chemical compound, exhibits anti-inflammatory, antitumor, antiviral, neuroprotective, and anxiolytic effects by modulating a variety of cellular signaling pathways including PI3K-Akt, p53, nuclear factor κB (NF-κB), mitogen-activated protein kinase (MAPK) pathways. In this study, its antiviral effect against herpes simplex virus (HSV) type 1 and 2 (HSV-1 and HSV-2) replication was investigated.&lt;h4>Results&lt;/h4>Wogonin suppressed HSV-2-induced cytopathic effect (CPE) and reduced viral mRNA transcription, viral protein synthesis, and infectious virion particle titers in a dose-dependent manner. A time-of-drug-addition assay demonstrated that wogonin acted as a postentry viral inhibitor. Wogonin also significantly reduced HSV-induced NF-κB a</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-05T15:21:14.57Z</modification><creation>2024-11-15T16:29:38.669Z</creation></dates><accession>S-EPMC7388529</accession><cross_references><pubmed>32723300</pubmed><doi>10.1186/s12866-020-01916-2</doi></cross_references></HashMap>