2017
DOI: 10.1039/c7ra07940k
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Versicotides D–F, new cyclopeptides with lipid-lowering activities

Abstract: Versicotides D–F, new cyclopeptides were isolated from a gorgonian-derived fungusAspergillus versicolorLZD-14-1 and showed lipid-lowering effects.

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Cited by 25 publications
(29 citation statements)
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“…][ In the present work, a soft coral associated fungal strain Aspergillus versicolor LZD‐44‐03, was examined by the NMR and MS spectra. The spectroscopic data revealed that the fermented extract contains unknown metabolites in comparison with the compounds obtained from the different strains of the same fungal species what we reported previously …”
Section: Introductionsupporting
confidence: 65%
“…][ In the present work, a soft coral associated fungal strain Aspergillus versicolor LZD‐44‐03, was examined by the NMR and MS spectra. The spectroscopic data revealed that the fermented extract contains unknown metabolites in comparison with the compounds obtained from the different strains of the same fungal species what we reported previously …”
Section: Introductionsupporting
confidence: 65%
“…Versicotides E and F possessed very rare structures that have two anthranilic acid residues and a proline in a single cyclic peptide system. They showed significant lipid-lowering activities by regulating cholesterol efflux and influx [58]. Chemical investigation on the culture extracts of mangrove-derived fungus Sarocladium kiliense HDN11-112 led to the discovery of two new cyclic depsipeptides saroclides A ( 127 ) and B ( 128 ).…”
Section: Peptidesmentioning
confidence: 99%
“…11 Later, the same group employed the OSMAC (one strain many compounds) approach on this fungus, resulting in the isolation and characterization of a new compound with structural similarities named versicotide C (3), 12 the rst natural cyclic hexapeptide containing two anthranilic acids (Anth). Further on, three new cyclopeptides were isolated from Aspergillus versicolor LZD-14-1 namely versicotides D-F, 13 along with the previously known versicotides A and B.…”
Section: Introductionmentioning
confidence: 98%
“…The structures of the obtained compounds were conrmed by MS, NMR and, in the case of versicotide A (1), by X-ray analysis. A deep analysis of NMR data ( 1 H, 13 C, COSY, HSQC and HMBC) was done in order to determine the adopted conformations in the used solvents, along with temperature variation studies.…”
Section: Introductionmentioning
confidence: 99%