2013
DOI: 10.1007/s10600-013-0552-x
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Metabolites from the Marine Isolate of the Fungus Aspergillus versicolor KMM 4644

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Cited by 6 publications
(9 citation statements)
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“…In addition to the isolation of the above new compounds, ten known analogues including brevianamide Q ( 7 ) [ 22 ], brevianamide R ( 8 ) [ 22 ], brevianamide K ( 9 ) [ 21 ], brevianamide W ( 10 ) [ 18 ], N -Prenyl-cyclo- l -tryptophyl- l -proline ( 11 ) [ 23 ], brevianamide F ( 12 ) [ 24 ], epi-deoxybrevianamide E ( 13 ) [ 25 ], cyclo-(tryptophyl-phenylalanyl) ( 14 ) [ 26 ], brevianamide M ( 15 ) [ 21 ] and brevianamide N ( 16 ) [ 21 ] were isolated and identified from this fungus. Their structures were determined by comparing their NMR and MS data with the reported in literatures.…”
Section: Resultsmentioning
confidence: 99%
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“…In addition to the isolation of the above new compounds, ten known analogues including brevianamide Q ( 7 ) [ 22 ], brevianamide R ( 8 ) [ 22 ], brevianamide K ( 9 ) [ 21 ], brevianamide W ( 10 ) [ 18 ], N -Prenyl-cyclo- l -tryptophyl- l -proline ( 11 ) [ 23 ], brevianamide F ( 12 ) [ 24 ], epi-deoxybrevianamide E ( 13 ) [ 25 ], cyclo-(tryptophyl-phenylalanyl) ( 14 ) [ 26 ], brevianamide M ( 15 ) [ 21 ] and brevianamide N ( 16 ) [ 21 ] were isolated and identified from this fungus. Their structures were determined by comparing their NMR and MS data with the reported in literatures.…”
Section: Resultsmentioning
confidence: 99%
“…In order to find potent antidiabetic natural products, all the compounds (1-16) were screened for the enzyme inhibitory activities against α-glucosidase and PTP1B (Table 3). Compared with the positive control acarbose (408 μM), all of the tested compounds, except compounds 5, 12, and 13, showed good to mod- In addition to the isolation of the above new compounds, ten known analogues including brevianamide Q (7) [22], brevianamide R (8) [22], brevianamide K (9) [21], brevianamide W (10) [18], N-Prenyl-cyclo-L-tryptophyl-L-proline (11) [23], brevianamide F (12) [24], epi-deoxybrevianamide E (13) [25], cyclo-(tryptophyl-phenylalanyl) ( 14) [26], brevianamide M (15) [21] and brevianamide N (16) [21] were isolated and identified from this fungus. Their structures were determined by comparing their NMR and MS data with the reported in literatures.…”
Section: Structural Elucidationmentioning
confidence: 99%
“…The cytotoxic activity against ascitic murine Ehrlich carcinoma cells and antiradical activity to DPPH were tested for all isolated compounds 1-10. Ethyl averantin (6) The influence of aversin on Hsp70 expression in Ehrlich carcinoma cells was evaluated. Up to a concentration 100 μM aversin did not effect Hsp70 expression in this cell type.…”
mentioning
confidence: 99%
“…The most intensive peak in the EI mass spectrum (m/z 256) corresponds to the ion [M-C 7 H 8 ] + , which is typical for diorcinolic diphenyl esters [2]. The 1 H NMR data analysis indicated the presence of five aromatic (δ H 6 1). The coupling constants of H-2 (δ H 6.36, t, J = 2.1 Hz), H-2' (δ H 6.25, d, J = 2.3 Hz) and H-6' (δ H 6.38, d, J = 2.6 Hz) indicated a meta-location of protons H-2, H-4 and H-6; H-2' and H-6'.…”
mentioning
confidence: 99%
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