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        <datestamp>2026-09-20T18:29:11Z</datestamp>
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          <dc:title>Phomporone A, a new cytosporone derivative from mangrove-derived fungus &lt;i&gt;Phomopsis asparagi&lt;/i&gt; ZMU-35-1</dc:title>
          <dc:creator>Chu-Ling Wu (25078172)</dc:creator>
          <dc:creator>Zu-Yan Zhong (25078175)</dc:creator>
          <dc:creator>Wei-Zhen Long (25078178)</dc:creator>
          <dc:creator>Min Wang (21070)</dc:creator>
          <dc:creator>Si-Wen Yuan (5370587)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Microbiology</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</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>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Hematology</dc:subject>
          <dc:subject>Infectious Diseases</dc:subject>
          <dc:subject>Plant Biology</dc:subject>
          <dc:subject>Phomporone A</dc:subject>
          <dc:subject>phomopsis asparagi</dc:subject>
          <dc:subject>mangrove-derived fungus</dc:subject>
          <dc:subject>antifungal activity</dc:subject>
          <dc:description>&lt;p&gt;A new polyketide, phomporone A (&lt;b&gt;1&lt;/b&gt;), along with three related analogues, cytosporone P (&lt;b&gt;2&lt;/b&gt;), cytosporone Q (&lt;b&gt;3&lt;/b&gt;), and cytosporone E (&lt;b&gt;4&lt;/b&gt;) were isolated from the mangrove-derived fungus &lt;i&gt;Phomopsis asparagi&lt;/i&gt; ZMU-35-1. The chemical structures of these compounds were elucidated through comprehensive spectroscopic analysis, including 1D and 2D NMR and high-resolution electrospray ionisation mass spectrometry (HR-ESIMS), and by comparison with previously reported spectral data. The antifungal activities of compounds &lt;b&gt;1&lt;/b&gt;–&lt;b&gt;4&lt;/b&gt; were evaluated against a panel of phytopathogenic fungi. Compound &lt;b&gt;1&lt;/b&gt; exhibited inhibitory activity against &lt;i&gt;Botryosphaeria dothidea&lt;/i&gt; and &lt;i&gt;Fusarium graminearum&lt;/i&gt;, with minimum inhibitory concentration (MIC) values of 50 and 100 μg/mL, respectively. Compound &lt;b&gt;2&lt;/b&gt; showed moderate activity against &lt;i&gt;Alternaria alternata&lt;/i&gt; with an MIC value of 100 μg/mL. Notably, compound &lt;b&gt;4&lt;/b&gt; displayed the most potent and broad-spectrum antifungal profile, inhibiting &lt;i&gt;B. dothidea&lt;/i&gt;, &lt;i&gt;Valsa mali&lt;/i&gt; Miyabe &amp; G. Yamada and &lt;i&gt;A. alternata&lt;/i&gt;, and with MIC values of 6.25, 50, and 100 μg/mL, respectively.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-20T18:29:11Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.33945842.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Phomporone_A_a_new_cytosporone_derivative_from_mangrove-derived_fungus_i_Phomopsis_asparagi_i_ZMU-35-1/33945842</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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