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A New N-methoxypyridone from the Co-Cultivation of Hawaiian Endophytic Fungi Camporesia sambuci FT1061 and Epicoccum sorghinum FT1062.


ABSTRACT: A new N-methoxypyridone analog (1), together with four known compounds, was isolated from the co-culture of Hawaiian endophytic fungi Camporesia sambuci FT1061 and Epicoccum sorghinum FT1062. The structure of the new compound was elucidated as 11S-hydroxy-1-methoxyfusaricide (1) by extensive spectroscopic analysis and comparison with the literature. The absolute configuration of 1 was determined by comparison with the experimental and calculated ECD spectra. The absolute configuration of compound 3 was investigated and renamed as (+)-epipyridone by comparison of the optical rotation and CD spectrum with those of 1. The other known compounds were identified as epicoccarine B (2), D8646-2-6 (4), and iso-D8646-2-6 (5). Compounds 4 and 5 showed modest inhibitory activity towards pathogenic fungi. Epicoccarine B (2) inhibited A2780 and TK-10 with an IC50 value of 22 ?M.

SUBMITTER: Li C 

PROVIDER: S-EPMC6152147 | biostudies-literature | 2017 Jul

REPOSITORIES: biostudies-literature

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A New N-methoxypyridone from the Co-Cultivation of Hawaiian Endophytic Fungi Camporesia sambuci FT1061 and Epicoccum sorghinum FT1062.

Li Chunshun C   Sarotti Ariel M AM   Yang Baojun B   Turkson James J   Cao Shugeng S  

Molecules (Basel, Switzerland) 20170712 7


A new <i>N</i>-methoxypyridone analog (<b>1</b>), together with four known compounds, was isolated from the co-culture of Hawaiian endophytic fungi <i>Camporesia sambuci</i> FT1061 and <i>Epicoccum sorghinum</i> FT1062. The structure of the new compound was elucidated as 11<i>S</i>-hydroxy-1-methoxyfusaricide (<b>1</b>) by extensive spectroscopic analysis and comparison with the literature. The absolute configuration of <b>1</b> was determined by comparison with the experimental and calculated E  ...[more]

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