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        <datestamp>2026-09-22T19:20:53Z</datestamp>
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          <dc:title>New bianthrone-type dimeric derivatives isolated from a mangrove-derived fungus &lt;i&gt;Hamigera paravellanea&lt;/i&gt; GXIMD 03119</dc:title>
          <dc:creator>Ya-Qi Chen (22896918)</dc:creator>
          <dc:creator>Cai-Qiong Zhu (19691417)</dc:creator>
          <dc:creator>Pei Cao (684902)</dc:creator>
          <dc:creator>Guang-Ying Chen (670978)</dc:creator>
          <dc:creator>Xiang-Xi Yi (17609566)</dc:creator>
          <dc:creator>Cheng-Hai Gao (6814535)</dc:creator>
          <dc:creator>Yong-Hong Liu (4745961)</dc:creator>
          <dc:creator>Kai Liu (159026)</dc:creator>
          <dc:creator>Meng Bai (2615941)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Ecology</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Virology</dc:subject>
          <dc:subject>Mangrove</dc:subject>
          <dc:subject>endophytic fungus</dc:subject>
          <dc:subject>Hamigera paravellanea</dc:subject>
          <dc:subject>secondary metabolites</dc:subject>
          <dc:subject>antibacterial activity</dc:subject>
          <dc:description>&lt;p&gt;Chemical investigation of the mangrove-derived fungus &lt;i&gt;Hamigera paravellanea&lt;/i&gt; GXIMD 03119 afforded two previously undescribed bianthrone-type dimers, emodin bianthrone C (&lt;b&gt;1&lt;/b&gt;) and emodin bianthrone D (&lt;b&gt;2&lt;/b&gt;), together with three known metabolites (&lt;b&gt;3&lt;/b&gt;-&lt;b&gt;5&lt;/b&gt;). The structures of two new compounds were established through detailed analysis of NMR spectroscopic data and HRESIMS evidence. The isolated compounds were evaluated for antibacterial activity, and compounds &lt;b&gt;1&lt;/b&gt; and &lt;b&gt;2&lt;/b&gt; inhibited &lt;i&gt;Staphylococcus aureus,&lt;/i&gt; each with an MIC value of 7.81 μg/mL. These results add new members to the emodin bianthrone family and further support mangrove-associated fungi as productive sources of bioactive secondary metabolites.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-22T19:20:53Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.33968659.v1</dc:identifier>
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          <dc:rights>CC BY 4.0</dc:rights>
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