New furoisocoumarins and isocoumarins from the mangrove endophytic fungus Aspergillus sp. 085242
The chemical investigation of the mangrove endophytic fungus sp. 085242 afforded eight isocoumarin derivatives - and one isoquinoline . Asperisocoumarins A and B ( and ) were new furoisocoumarins, and asperisocoumarins E and F ( and ) were new isocoumarins. Their structures were established by analy...
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Veröffentlicht in: | Beilstein journal of organic chemistry 2016-09, Vol.12 (1), p.2077-2085 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
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Zusammenfassung: | The chemical investigation of the mangrove endophytic fungus
sp. 085242 afforded eight isocoumarin derivatives
-
and one isoquinoline
. Asperisocoumarins A and B (
and
) were new furoisocoumarins, and asperisocoumarins E and F (
and
) were new isocoumarins. Their structures were established by analysis of their spectroscopic data and the absolute configuration of compound
was unambiguously determined by X-ray structure analysis and ECD calculation. Moreover, the absolute configurations of compounds
-
were assigned by comparison of their ECD spectra with isocoumarins described in the literature. Asperisocoumarins C and D (
and
) were fully characterized spectroscopically and isolated from a natural source for the first time. Asperisocoumarins A-D (
-
) related to the class of furo[3,2-
]isocoumarins are rarely occurring in natural sources. Compounds
,
, and
showed moderate α-glucosidase inhibitory activity with IC
of 87.8, 52.3, and 95.6 μM, respectively. In addition, compounds
and
exhibited weak radical scavenging activity with EC
values of 125 and 138 μM, respectively. |
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ISSN: | 1860-5397 2195-951X 1860-5397 |
DOI: | 10.3762/bjoc.12.196 |