Structurally Diverse Polycyclic Salicylaldehyde Derivative Enantiomers from a Marine-Derived Fungus Eurotium sp. SCSIO F452

To enlarge the chemical diversity of sp. SCSIO F452, a talented marine-derived fungus, we further investigated its chemical constituents from a large-scale fermentation with modified culture. Four pairs of new salicylaldehyde derivative enantiomers, euroticins F-I ( - ), as well as a known one eurot...

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Veröffentlicht in:Marine drugs 2021-09, Vol.19 (10), p.543
Hauptverfasser: Zhong, Wei-Mao, Wei, Xiao-Yi, Chen, Yu-Chan, Zeng, Qi, Wang, Jun-Feng, Shi, Xue-Feng, Tian, Xin-Peng, Zhang, Wei-Min, Wang, Fa-Zuo, Zhang, Si
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Sprache:eng
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Zusammenfassung:To enlarge the chemical diversity of sp. SCSIO F452, a talented marine-derived fungus, we further investigated its chemical constituents from a large-scale fermentation with modified culture. Four pairs of new salicylaldehyde derivative enantiomers, euroticins F-I ( - ), as well as a known one eurotirumin ( ) were isolated and characterized. Compound features an unprecedented constructed 6/6/6/5 tetracyclic structures, while and represent two new types of 6/6/5 scaffolds. Their structures were established by comprehensive spectroscopic analyses, X-ray diffraction, C NMR, and electronic circular dichroism calculations. Selected compounds showed significant inhibitory activity against α-glucosidase and moderate cytotoxic activities against SF-268, MCF-7, HepG2, and A549 cell lines.
ISSN:1660-3397
1660-3397
DOI:10.3390/md19100543