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Antifungal Prenylated Diphenyl Ethers from Arthrinium arundinis, an Endophytic Fungus Isolated from the Leaves of Tobacco (Nicotiana tabacum L.).


ABSTRACT: An endophytic fungus Arthrinium arundinis TE-3 was isolated and purified from the fresh leaves of cultivated tobacco (Nicotiana tabacum L.). Chemical investigation on this fungal strain afforded three new prenylated diphenyl ethers (1-3) as well as three known analogues (4-6). Structure elucidation of the isolated compounds was carried out by analysis of 1D and 2D nuclear magnetic resonance (NMR) and high-resolution electrospray ionization mass spectroscopy (HRESIMS) spectra, as well as by comparison of those data with literature data. The absolute configuration of the stereogenic center at C-8 in 1 was assigned by comparison of the experimental and calculated ECD spectra. Compounds 1 and 2 showed selective antifungal activity against Mucor hiemalis with minimum inhibitory concentration (MIC) values of 8 and 4 ?g/mL, respectively. Compounds 5 and 6 exhibited inhibitory activity against Alteraria alternata with an MIC value of 8 ?g/mL. In the cytotoxic assay, 2, 5, and 6 displayed moderate in vitro cytotoxicity against the human monocytic cell line (THP-1 cell line), with IC50 values of 40.2, 28.3, and 25.9 ?M, respectively. This study indicated that endophytic fungi possess great potential for exploring new bioactive secondary metabolites.

SUBMITTER: Zhang P 

PROVIDER: S-EPMC6320909 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Antifungal Prenylated Diphenyl Ethers from <i>Arthrinium arundinis</i>, an Endophytic Fungus Isolated from the Leaves of Tobacco (<i>Nicotiana tabacum</i> L.).

Zhang Peng P   Li Xin X   Yuan Xiao-Long XL   Du Yong-Mei YM   Wang Bin-Gui BG   Zhang Zhong-Feng ZF  

Molecules (Basel, Switzerland) 20181202 12


An endophytic fungus <i>Arthrinium arundinis</i> TE-3 was isolated and purified from the fresh leaves of cultivated tobacco (<i>Nicotiana tabacum</i> L.). Chemical investigation on this fungal strain afforded three new prenylated diphenyl ethers (<b>1</b>-<b>3</b>) as well as three known analogues (<b>4</b>-<b>6</b>). Structure elucidation of the isolated compounds was carried out by analysis of 1D and 2D nuclear magnetic resonance (NMR) and high-resolution electrospray ionization mass spectrosc  ...[more]

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