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New Xanthones with Antiagricultural Fungal Pathogen Activities from the Endophytic Fungus Diaporthe goulteri L17
Six new xanthone dimers, diaporxanthones A–F (1–6), and an unusual xanthone monomer diaporxanthone G (7), in addition to seven known analogues (8–14), were isolated and identified from endophytic Diaporthe goulteri L17 harbored in the fruits of the salt-tolerant plant Vitex trifolia. The chemical st...
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Published in: | Journal of agricultural and food chemistry 2021-09, Vol.69 (38), p.11216-11224 |
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container_end_page | 11224 |
container_issue | 38 |
container_start_page | 11216 |
container_title | Journal of agricultural and food chemistry |
container_volume | 69 |
creator | Peng, Xiaoping Sun, Fusheng Li, Gang Wang, Cong Zhang, Yuhan Wu, Changzheng Zhang, Chunyang Sun, Yong Wu, Siyi Zhang, Yuxiang Zong, Hui Guo, Rui Lou, Hongxiang |
description | Six new xanthone dimers, diaporxanthones A–F (1–6), and an unusual xanthone monomer diaporxanthone G (7), in addition to seven known analogues (8–14), were isolated and identified from endophytic Diaporthe goulteri L17 harbored in the fruits of the salt-tolerant plant Vitex trifolia. The chemical structures of these metabolites were elucidated on the basis of nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, and reported data in the literature. Their absolute configurations were established by single-crystal X-ray diffraction analysis together with time-dependent density functional theory electronic circular dichroism calculations. Among these compounds, compounds 1 and 6 exhibited moderate antifungal activities against Nectria sp. and Colletotrichum musae and compound 4 showed significant cytotoxicity against all selected five cancer cell lines. |
doi_str_mv | 10.1021/acs.jafc.1c03513 |
format | article |
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The chemical structures of these metabolites were elucidated on the basis of nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, and reported data in the literature. Their absolute configurations were established by single-crystal X-ray diffraction analysis together with time-dependent density functional theory electronic circular dichroism calculations. 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Agric. Food Chem</addtitle><date>2021-09-29</date><risdate>2021</risdate><volume>69</volume><issue>38</issue><spage>11216</spage><epage>11224</epage><pages>11216-11224</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><abstract>Six new xanthone dimers, diaporxanthones A–F (1–6), and an unusual xanthone monomer diaporxanthone G (7), in addition to seven known analogues (8–14), were isolated and identified from endophytic Diaporthe goulteri L17 harbored in the fruits of the salt-tolerant plant Vitex trifolia. The chemical structures of these metabolites were elucidated on the basis of nuclear magnetic resonance, high-resolution electrospray ionization mass spectrometry, and reported data in the literature. Their absolute configurations were established by single-crystal X-ray diffraction analysis together with time-dependent density functional theory electronic circular dichroism calculations. 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source | American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list) |
subjects | Agricultural and Environmental Chemistry |
title | New Xanthones with Antiagricultural Fungal Pathogen Activities from the Endophytic Fungus Diaporthe goulteri L17 |
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