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Fused multicyclic polyketides with a two-spiro-carbon skeleton from mangrove-derived endophytic fungus Epicoccum nigrum SCNU-F0002.


ABSTRACT: A pair of uncommon fused multicyclic polyketides with a two- spiro-carbon skeleton, (±)-isoepicolactone, (±)-1, and one new isobenzofuranone monomer (4), together with four other known biosynthetically related compounds were isolated from the fermentation of an endophytic fungus, Epicoccum nigrum SCNU-F0002, which was isolated from the fresh fruit of the mangrove plant Acanthus ilicifolius L. Comprehensive spectroscopic analysis, X-ray crystallography, together with calculated ECD, were employed to define the structures. The antibacterial and COX-2 inhibitory activities of the compounds (1-6) were evaluated. A possible biogenetic pathway of (±)-isoepicolactone was confirmed.

SUBMITTER: Yan Z 

PROVIDER: S-EPMC9055859 | biostudies-literature | 2020 Aug

REPOSITORIES: biostudies-literature

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Fused multicyclic polyketides with a two-spiro-carbon skeleton from mangrove-derived endophytic fungus <i>Epicoccum nigrum</i> SCNU-F0002.

Yan Zhangyuan Z   Li Jialin J   Ye Geting G   Chen Tao T   Li Meimei M   Liang Yanmin Y   Long Yuhua Y  

RSC advances 20200803 48


A pair of uncommon fused multicyclic polyketides with a two- spiro-carbon skeleton, (±)-isoepicolactone, (±)-1, and one new isobenzofuranone monomer (4), together with four other known biosynthetically related compounds were isolated from the fermentation of an endophytic fungus, <i>Epicoccum nigrum</i> SCNU-F0002, which was isolated from the fresh fruit of the mangrove plant <i>Acanthus ilicifolius L</i>. Comprehensive spectroscopic analysis, X-ray crystallography, together with calculated ECD,  ...[more]

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