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    <identifier>10.57760/sciencedb.33494</identifier>
    <datestamp>2025-12-18T18:11:50Z</datestamp>
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  <dc:date>2025-12-18</dc:date>
  <dc:title>Candindoles A and B, heterozygous terphenyl-indole alkaloids with antifungal and cytotoxic activities from the marine-derived fungus Aspergillus candidus HNNU0546</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.33494</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Three previously undescribed indole alkaloids candindoles A-C (1-3), along with five known analogues (4-8), were isolated from the marine-derived fungus Aspergillus candidus HNNU0546. Structurally, 1 and 2 represent the first terphenyl-indole piperazine alkaloid hybrids, featuring unprecedented backbones. Their structures including absolute configurations, were elucidated by extensive spectroscopic methods, DP4+ probability analysis and ECD calculations. A plausible biosynthetic pathway for 1 is proposed. Compound 1 exhibited moderate growth-inhibitory activity against the plant pathogenic fungus of Alternaria sp. with an EC50 value of 19.21 &amp;plusmn; 0.26 &amp;micro;M, while compounds 1 and 2 showed significant cytotoxicity towards human rhabdomyosarcoma cells A673 with IC50 values of 7.72 and 8.89 &amp;micro;M, respectively, comparable to the positive control cisplatin.&amp;nbsp;</dc:description>
  <dc:subject>Aspergillus candidus; cold-seep-derived fungus; terphenyl-indole piperazine alkaloid; anti-fungal; cytotoxicity</dc:subject>
  <dc:creator>Liu Yiyi</dc:creator>
  <dc:creator>Chen Haixin</dc:creator>
  <dc:creator>Chen Guangying</dc:creator>
  <dc:creator>Nong Xuhua</dc:creator>
  <dc:creator>Han Zhuang</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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