2018
DOI: 10.3390/md16090335
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Cytotoxic Tetrahydroxanthone Dimers from the Mangrove-Associated Fungus Aspergillus versicolor HDN1009

Abstract: Three new tetrahydroxanthone dimers, 5-epi-asperdichrome (1), versixanthones N (2), and O (3), were isolated from the mangrove-derived fungus Aspergillus versicolor HDN1009. Their structures, including the absolute configurations, were elucidated by NMR, HRMS, and circular dichroism (CD) experiments. Among them, compound 1 was the second example of tetrahydroxanthone dimers, which dimerized by a rare diaryl ether linkage and showed promising antibacterial activities against Vibrio parahemolyticus, Bacillus sub… Show more

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Cited by 36 publications
(40 citation statements)
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“…Semi-preparative HPLC (YMC Co., Ltd., Kyoto, Japan) was performed on an ODS column (YMC-Pack ODS-A, 10 × 250 mm, 5 μm, 3 mL/min). Medium-pressure liquid chromatography (MPLC) was performed on a Bona-Agela CHEETAHTM HP100 (Beijing Agela Technologies Co., Ltd., Beijing, China) [26].…”
Section: Methodsmentioning
confidence: 99%
“…Semi-preparative HPLC (YMC Co., Ltd., Kyoto, Japan) was performed on an ODS column (YMC-Pack ODS-A, 10 × 250 mm, 5 μm, 3 mL/min). Medium-pressure liquid chromatography (MPLC) was performed on a Bona-Agela CHEETAHTM HP100 (Beijing Agela Technologies Co., Ltd., Beijing, China) [26].…”
Section: Methodsmentioning
confidence: 99%
“…Then it has antidiabetic activity by preventing the reducing the impact of carbohydrates in blood ( Figure 7 b). Three novel compounds 204 , 205 and 206 were obtained from the fungus A. versicolor HDN1009 ( Figure 7 b) [ 120 ]. Structure 204 was showed hopeful antibacterial activities towards both G-positive and G-negatie bacteria .…”
Section: Main Textmentioning
confidence: 99%
“…Aspergillus versicolor , a slow-growing filamentous fungus, normally are found in air, soil, marine sediment, corrupted plants, and agricultural products. Previous chemical investigations on the fungus Aspergillus versicolor from different environments have resulted in the identification of new secondary metabolites with a variety of structures, such as alkaloids [4,5,6,7,8,9], anthraquinones [10,11,12,13,14], xanthones [15,16,17,18,19], diphenyl ethers [20,21], lactones [22,23,24,25,26], peptides [27], polyketide [28], terpenoids [29,30], and varicuothiols [31].…”
Section: Introductionmentioning
confidence: 99%