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        <datestamp>2026-10-01T05:37:36Z</datestamp>
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          <dc:title>Table 1_Exploration of the mechanisms and active compounds of Scutellaria barbata D. Don against influenza A (H1N1) virus.xlsx</dc:title>
          <dc:creator>Ying Yang (24175)</dc:creator>
          <dc:creator>Junjing Shao (25152744)</dc:creator>
          <dc:creator>Lin Hou (177757)</dc:creator>
          <dc:creator>Shihao Sun (3766798)</dc:creator>
          <dc:creator>Guihong Qi (18000811)</dc:creator>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>active compounds</dc:subject>
          <dc:subject>antiviral</dc:subject>
          <dc:subject>H1N1</dc:subject>
          <dc:subject>mechanisms</dc:subject>
          <dc:subject>Scutellaria barbata D. Don</dc:subject>
          <dc:description>Introduction&lt;p&gt;Scutellaria barbata D. Don (S. barbata), a traditional Chinese medicinal herb widely used for its heat-clearing and detoxifying properties, has shown broad-spectrum antiviral potential. However, its anti-H1N1 activity and underlying mechanisms remain to be fully elucidated.&lt;/p&gt;Methods&lt;p&gt;In this study, the anti-H1N1 activity and underlying mechanisms of S. barbata extract were investigated using H1N1-infected MDCK cells and BALB/c mice. Transcriptomic analysis followed by mRNA and protein-level validation was performed to characterize its molecular effects, while UPLC-Q-Orbitrap-MS was used to identify blood-absorbed constituents. Potential active compounds were subsequently screened by integrating the absorbed constituents with network pharmacology and further validated in vitro and in vivo.&lt;/p&gt;Results&lt;p&gt;S. barbata extract markedly inhibited H1N1 replication in MDCK cells (IC&lt;sub&gt;50&lt;/sub&gt; = 42.87 μg/mL; CC&lt;sub&gt;50&lt;/sub&gt; &gt; 500 μg/mL) and reduced viral burden and pulmonary inflammation in infected mice. Mechanistically, S. barbata treatment suppressed the Toll-like receptor, NF-κB, and chemokine signaling pathways, suggesting coordinated regulation of antiviral and inflammatory responses. Among the blood-absorbed constituents, baicalein and chrysoeriol were identified as key candidate active compounds and exhibited potent anti-H1N1 activity in vitro and in vivo (IC&lt;sub&gt;50&lt;/sub&gt; = 13.80 and 11.10 μM, respectively).&lt;/p&gt;Discussion&lt;p&gt;Collectively, these findings demonstrate that S. barbata exerts anti-H1N1 effects through a combination of direct inhibition of viral replication and modulation of excessive inflammatory responses, with baicalein and chrysoeriol representing important contributors to its antiviral activity.&lt;/p&gt;</dc:description>
          <dc:date>2026-10-01T05:37:36Z</dc:date>
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          <dc:identifier>10.3389/fmicb.2026.1945077.s001</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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