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New Benzofuranoids and Phenylpropanoids from the Mangrove Endophytic Fungus, Aspergillus sp. ZJ-68.


ABSTRACT: Three new benzofuranoids, asperfuranoids A-C (1-3), two new phenylpropanoid derivatives (6 and 7), and nine known analogues (4, 5, and 8-14) were isolated from the liquid substrate fermentation cultures of the mangrove endopytic fungus Aspergillus sp. ZJ-68. The structures of the new compounds were determined by extensive spectroscopic data interpretation. The absolute configurations of 1-3 were assigned via the combination of Mosher's method, and experimental and calculated electronic circular dichroism (ECD) data. Compounds 4 and 5 were a pair of enantiomers and their absolute configurations were established for the first time on the basis of their ECD spectra aided with ECD calculations. All isolated compounds (1-14) were evaluated for their enzyme inhibitory activity against ?-glucosidase and antibacterial activities against four pathogenic bacteria (Staphylococcus aureus, Escherichia coli, Bacillus subtilis, and Pseudomonas aeruginosa). Among them, compound 6 exhibited potent inhibitory activity against ?-glucosidase in a standard in vitro assay, with an IC50 value of 12.4 ?M, while compounds 8 and 11 showed activities against S. aureus, E. coli, and B. subtilis, with MIC values in the range of 4.15 to 12.5 ?g/mL.

SUBMITTER: Cai R 

PROVIDER: S-EPMC6723808 | biostudies-literature | 2019 Aug

REPOSITORIES: biostudies-literature

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New Benzofuranoids and Phenylpropanoids from the Mangrove Endophytic Fungus, <i>Aspergillus</i> sp. ZJ-68.

Cai Runlin R   Jiang Hongming H   Zang Zhenming Z   Li Chunyuan C   She Zhigang Z  

Marine drugs 20190818 8


Three new benzofuranoids, asperfuranoids A-C (<b>1</b>-<b>3</b>), two new phenylpropanoid derivatives (<b>6</b> and <b>7</b>), and nine known analogues (<b>4</b>, <b>5</b>, and <b>8</b>-<b>14</b>) were isolated from the liquid substrate fermentation cultures of the mangrove endopytic fungus <i>Aspergillus</i> sp. ZJ-68. The structures of the new compounds were determined by extensive spectroscopic data interpretation. The absolute configurations of <b>1</b>-<b>3</b> were assigned via the combina  ...[more]

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