New Polyketide and Butenolide Derivatives from the Mangrove Fungus Aspergillus spelaeus SCSIO 41433

Two new racemic mixtures, including a polyketide, (±)-penilactone F (<b>1</b>), and a butenolide, (±) phenylbutyrolactone IIa (<b>2</b>), were isolated from the mangrove sediment-derived strain <i>Aspergillus spelaeus</i> SCSIO 41433. Additionally, 20 known compounds were isolated, including four penicillin-like compounds (<b>11</b>-<b>14</b>), three alkaloids (<b>15</b>-<b>17</b>), one sesquiterpene (<b>18</b>), and four phenolic acids (<b>19</b>-<b>22</b>). Their structures were elucidated through NMR spectroscopy, HRESIMS, X-ray diffraction, and ECD calculations. In the PDE4 inhibitory activity and anticancer cell activity assays, compounds <b>2</b>, <b>3</b>, <b>5</b>, <b>8</b>, <b>9</b>, <b>11</b>-<b>14</b>, and <b>16</b> exhibited weak PDE4 inhibitory activity at a concentration of 10 µM, Compound <b>11</b> demonstrated potent inhibitory effects against six cancer cell lines (MDA-MB-231, MDA-MB-435, HCT116, SNB-19, PC3, and A549), with IC<sub>50</sub> values ranging from 3.4 to 23.7 µM.

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Publication Details

Journal
Marine Drugs
Published
2025-06-13
DOI
https://doi.org/10.3390/md23060251
Citations
4
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
5.58

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article

New Polyketide and Butenolide Derivatives from the Mangrove Fungus Aspergillus spelaeus SCSIO 41433

Chun Yang, Bin Yang, Jiaqi Liang, Xuefeng Zhou et al.
4 citations
Marine Drugs
Microbial Natural Products and Biosynthesis
5.58
article

New Polyketide and Butenolide Derivatives from the Mangrove Fungus Aspergillus spelaeus SCSIO 41433

Chun Yang, Bin Yang, Jiaqi Liang, Xuefeng Zhou, Huaming Tao, Zimin Xiao, Jian Cai, Jie Yuan
article en
4 citations

Abstract

Two new racemic mixtures, including a polyketide, (±)-penilactone F (<b>1</b>), and a butenolide, (±) phenylbutyrolactone IIa (<b>2</b>), were isolated from the mangrove sediment-derived strain <i>Aspergillus spelaeus</i> SCSIO 41433. Additionally, 20 known compounds were isolated, including four penicillin-like compounds (<b>11</b>-<b>14</b>), three alkaloids (<b>15</b>-<b>17</b>), one sesquiterpene (<b>18</b>), and four phenolic acids (<b>19</b>-<b>22</b>). Their structures were elucidated through NMR spectroscopy, HRESIMS, X-ray diffraction, and ECD calculations. In the PDE4 inhibitory activity and anticancer cell activity assays, compounds <b>2</b>, <b>3</b>, <b>5</b>, <b>8</b>, <b>9</b>, <b>11</b>-<b>14</b>, and <b>16</b> exhibited weak PDE4 inhibitory activity at a concentration of 10 µM, Compound <b>11</b> demonstrated potent inhibitory effects against six cancer cell lines (MDA-MB-231, MDA-MB-435, HCT116, SNB-19, PC3, and A549), with IC<sub>50</sub> values ranging from 3.4 to 23.7 µM.

Marine DrugsVol. 23(6)
Sun Yat-sen University (CN), Chinese Academy of Sciences (CN), Institute of Oceanology (CN), South China Sea Institute Of Oceanology (CN), University of Chinese Academy of Sciences (CN), Southern Medical University (CN)
Natural Science Foundation of Guangdong Province, South China Sea Institute of Oceanology, Chinese Academy of Sciences
Openalex Percentile: Top 4%
Microbial Natural Products and Biosynthesis
5.58
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