Discovery of a Dimeric Zinc Complex and Five Cyclopentenone Derivatives from the Sponge-Associated Fungus Aspergillus ochraceopetaliformis

In devotion to investigating structurally novel and biologically active marine natural products, a dimer of a zinc complex, dizinchydroxyneoaspergillin (1), aspernones A–E (2–6), five cyclopentenone derivatives together with known polyketides (7–10), and neoaspergillic acid analogues (11–14) were is...

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Published inACS omega Vol. 6; no. 13; pp. 8942 - 8949
Main Authors Guo, Cui, Wang, Pei, Pang, Xiaoyan, Lin, Xiuping, Liao, Shengrong, Yang, Bin, Zhou, Xuefeng, Wang, Junfeng, Liu, Yonghong
Format Journal Article
LanguageEnglish
Published United States American Chemical Society 06.04.2021
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Summary:In devotion to investigating structurally novel and biologically active marine natural products, a dimer of a zinc complex, dizinchydroxyneoaspergillin (1), aspernones A–E (2–6), five cyclopentenone derivatives together with known polyketides (7–10), and neoaspergillic acid analogues (11–14) were isolated from the sponge-associated fungus Aspergillus ochraceopetaliformis SCSIO 41018. Their structures were elucidated on the basis of spectroscopic analysis, electronic circular dichroism (ECD) analysis, and X-ray diffraction. Dizinchydroxyneoaspergillin (1) displayed significant bactericide effects toward methicillin-resistant Staphyloccocus aureus, Staphyloccocus aureus, Enterococcus faecalis, Acinetobacter baumannii, and Klebsiella pneumonia with MIC values of 0.45–7.8 μg/mL and moderate in vitro cytotoxic activities against the K562, BEL-7402, and SGC-7901 cell lines with IC50 values of 12.88 ± 0.14, 15.83 ± 0.23, and 15.08 ± 0.62 μM, respectively. This is the first time to report the dimer of the zinc complex of hydroxyneoaspergillic acid conjunction at Zn–N-4 by a coordination bond. Additionally, compound 1 displayed significant antibacterial and cytotoxic activities, which would be a promising drug lead and could attract much attention from both chemists and pharmacists.
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ISSN:2470-1343
2470-1343
DOI:10.1021/acsomega.0c06218