Oxirapentyns F–K from the Marine-Sediment-Derived Fungus Isaria felina KMM 4639
Оксиропентины F–K из гриба Isaria felina KMM 4639, выделенного из морских донных отложений
2014-06-09
SCID: 54.1/3vpvvcfa
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Isaria felina KMM 4639chromene derivativescyclodepsipeptides isoisariin Bisaridin Eoxirapentyns F–K
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Abstract (AI)
Six new highly oxygenated chromene derivatives, oxirapentyns F-K (2-7), one new polyketide (8), one new benzofurane (9), and two known cyclodepsipeptides, isoisariin B and isaridin E, were isolated from the lipophilic extract of the marine-derived fungus Isaria felina KMM 4639. The structures of compounds 2-9 were determined using spectroscopic methods. The relative configurations of compounds 2-7 were established through a combination of NOE data and spin coupling constants, and these results were confirmed by X-ray crystallographic analysis of 4. The absolute structures of all oxirapentyns were assumed based on their biogenetic relationship and confirmed using the modified Mosher's method on 2 and 7. Isariketide (8) showed moderate cytotoxicity toward HL-60 cells.
Key Findings
1
Absolute configurations of all oxirapentyns were assumed by biogenetic relationship and experimentally confirmed for compounds 2 and 7 using the modified Mosher's method.
2
Isariketide (compound 8) exhibited moderate cytotoxicity against HL-60 human leukemia cells.
3
One new polyketide (isariketide, compound 8) and one new benzofuran (compound 9) were also isolated from the same fungal extract.
4
Six new highly oxygenated chromene derivatives, named oxirapentyns F–K (compounds 2–7), were isolated from the marine-derived fungus Isaria felina KMM 4639.
5
Structures of compounds 2–9 were elucidated using spectroscopic methods, with relative configurations of oxirapentyns 2–7 assigned by NOE data and spin coupling constants.
6
Two known cyclodepsipeptides, isoisariin B and isaridin E, were co-isolated from the lipophilic extract.
7
X-ray crystallography of compound 4 confirmed the relative configurations determined for the oxirapentyns.
Research Object
Oxirapentyns F–K and related secondary metabolites isolated from the marine-sediment-derived fungus Isaria felina KMM 4639
Research Subject
Structural characterization (including stereochemistry determination by NMR, NOE, spin–spin coupling, X-ray crystallography, and Mosher's method) and bioactivity assessment (cytotoxicity of isariketide) of the isolated compounds
Publication Details
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2014-06-09
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