HPLC–UV-Guided Discovery of Eurotamines A–F: Six Pairs of Isoquinoline Derivative Enantiomers from Marine-Derived Fungus <i>Eurotium</i> sp. SCSIO F452

Six pairs of unprecedented isoquinoline derivative enantiomers were obtained by HPLC-UV-guided isolation from the salicylaldehyde-producing marine fungus <i>Eurotium</i> sp. SCSIO F452. Their structures were characterized by spectroscopic analyses, X-ray diffraction, and electronic circular dichroism calculations. They represent unusual groups of oxidized, prenylated benzopyridines with a C<sub>7</sub> side chain cyclized in different patterns, generating 6/6/5/6 (<b>1</b>-<b>3</b>), 6/6 (<b>4</b> and <b>5</b>), and 6/6/6 (<b>6</b>) ring systems. Selected isomers exhibited weak cytotoxic activities against a panel of cancer cell lines.

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Publication Details

Journal
Organic Letters
Published
2025-10-17
DOI
https://doi.org/10.1021/acs.orglett.5c03641
Citations
1
Primary Topic
Asymmetric Synthesis and Catalysis
Type
article
Field-Weighted Citation Impact
0.94
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article

HPLC–UV-Guided Discovery of Eurotamines A–F: Six Pairs of Isoquinoline Derivative Enantiomers from Marine-Derived Fungus Eurotium sp. SCSIO F452

Yuchan Chen, Fa‐Zuo Wang, Xinpeng Tian, Weimao Zhong et al.
1 citations
Organic Letters
Asymmetric Synthesis and Catalysis
0.94
article

HPLC–UV-Guided Discovery of Eurotamines A–F: Six Pairs of Isoquinoline Derivative Enantiomers from Marine-Derived Fungus Eurotium sp. SCSIO F452

Yuchan Chen, Fa‐Zuo Wang, Xinpeng Tian, Weimao Zhong, István Molnár, Xiaoyi Wei, Yi-Hao Che, Weimin Zhang, Junfeng Wang, Si Zhang, Qi Zeng, Hao Yin, Lin Wang
article en
1 citations

Abstract

Six pairs of unprecedented isoquinoline derivative enantiomers were obtained by HPLC-UV-guided isolation from the salicylaldehyde-producing marine fungus <i>Eurotium</i> sp. SCSIO F452. Their structures were characterized by spectroscopic analyses, X-ray diffraction, and electronic circular dichroism calculations. They represent unusual groups of oxidized, prenylated benzopyridines with a C<sub>7</sub> side chain cyclized in different patterns, generating 6/6/5/6 (<b>1</b>-<b>3</b>), 6/6 (<b>4</b> and <b>5</b>), and 6/6/6 (<b>6</b>) ring systems. Selected isomers exhibited weak cytotoxic activities against a panel of cancer cell lines.

Organic LettersVol. 27(43)
Chinese Academy of Sciences (CN), Beijing Botanical Garden (CN), Institute of Oceanology (CN), Guangdong Academy of Sciences (CN), South China Sea Institute Of Oceanology (CN), Southern Marine Science and Engineering Guangdong Laboratory (Guangzhou) (CN), South China Botanical Garden (CN), Institute of Microbiology (CN), University of Chinese Academy of Sciences (CN), VTT Technical Research Centre of Finland (FI)
Openalex Percentile: Top 20%
Asymmetric Synthesis and Catalysis
0.94
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