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Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002
Five previously undescribed epoxy octa-hydronaphthalene polyketides, altereporenes A–E (1–5) were isolated from rice culture of the endophytic fungus Alternaria sp. YUD20002 derived from the tubers of Solanum tuberosum. Their structures were determined on the basis of comprehensive spectroscopic ana...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364171/ https://www.ncbi.nlm.nih.gov/pubmed/36043060 http://dx.doi.org/10.1039/d2ra03917f |
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author | Xia, Dan-Dan Duan, Hao-Jie Xie, Fei Xie, Tian-Peng Zhang, Yan Sun, Yue Lu, Jian-Mei Gao, Yu-Hong Zhou, Hao Ding, Zhong-Tao |
author_facet | Xia, Dan-Dan Duan, Hao-Jie Xie, Fei Xie, Tian-Peng Zhang, Yan Sun, Yue Lu, Jian-Mei Gao, Yu-Hong Zhou, Hao Ding, Zhong-Tao |
author_sort | Xia, Dan-Dan |
collection | PubMed |
description | Five previously undescribed epoxy octa-hydronaphthalene polyketides, altereporenes A–E (1–5) were isolated from rice culture of the endophytic fungus Alternaria sp. YUD20002 derived from the tubers of Solanum tuberosum. Their structures were determined on the basis of comprehensive spectroscopic analyses, while the absolute configurations were elucidated by the comparison of experimental and calculated specific rotations. Meanwhile, the antimicrobial, cytotoxic, anti-inflammatory and acetylcholinesterase inhibitory activities of compounds 1–5 were also investigated. |
format | Online Article Text |
id | pubmed-9364171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-93641712022-08-29 Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 Xia, Dan-Dan Duan, Hao-Jie Xie, Fei Xie, Tian-Peng Zhang, Yan Sun, Yue Lu, Jian-Mei Gao, Yu-Hong Zhou, Hao Ding, Zhong-Tao RSC Adv Chemistry Five previously undescribed epoxy octa-hydronaphthalene polyketides, altereporenes A–E (1–5) were isolated from rice culture of the endophytic fungus Alternaria sp. YUD20002 derived from the tubers of Solanum tuberosum. Their structures were determined on the basis of comprehensive spectroscopic analyses, while the absolute configurations were elucidated by the comparison of experimental and calculated specific rotations. Meanwhile, the antimicrobial, cytotoxic, anti-inflammatory and acetylcholinesterase inhibitory activities of compounds 1–5 were also investigated. The Royal Society of Chemistry 2022-08-10 /pmc/articles/PMC9364171/ /pubmed/36043060 http://dx.doi.org/10.1039/d2ra03917f Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/ |
spellingShingle | Chemistry Xia, Dan-Dan Duan, Hao-Jie Xie, Fei Xie, Tian-Peng Zhang, Yan Sun, Yue Lu, Jian-Mei Gao, Yu-Hong Zhou, Hao Ding, Zhong-Tao Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 |
title | Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 |
title_full | Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 |
title_fullStr | Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 |
title_full_unstemmed | Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 |
title_short | Altereporenes A–E, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus Alternaria sp. YUD20002 |
title_sort | altereporenes a–e, five epoxy octa-hydronaphthalene polyketides produced by an endophytic fungus alternaria sp. yud20002 |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9364171/ https://www.ncbi.nlm.nih.gov/pubmed/36043060 http://dx.doi.org/10.1039/d2ra03917f |
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