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Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata

Two new tetranorlabdane diterpenoids, named botryosphaerins G (1) and H (2), were isolated from the solid fermentation products of Botryosphaeria sp. P483 along with seven known tetranorlabdane diterpenes (3–9). Their structures were elucidated by extensive analysis, including 1D and 2D nuclear magn...

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Detalles Bibliográficos
Autores principales: Chen, Yan-Mei, Yang, Yin-He, Li, Xiao-Nian, Zou, Cheng, Zhao, Pei-Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331882/
https://www.ncbi.nlm.nih.gov/pubmed/26393542
http://dx.doi.org/10.3390/molecules200916924
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author Chen, Yan-Mei
Yang, Yin-He
Li, Xiao-Nian
Zou, Cheng
Zhao, Pei-Ji
author_facet Chen, Yan-Mei
Yang, Yin-He
Li, Xiao-Nian
Zou, Cheng
Zhao, Pei-Ji
author_sort Chen, Yan-Mei
collection PubMed
description Two new tetranorlabdane diterpenoids, named botryosphaerins G (1) and H (2), were isolated from the solid fermentation products of Botryosphaeria sp. P483 along with seven known tetranorlabdane diterpenes (3–9). Their structures were elucidated by extensive analysis, including 1D and 2D nuclear magnetic resonance (NMR) spectroscopy, and high-resolution electrospray ionization mass spectrometry (HR-ESI-MS). Their absolute configuration was confirmed by single-crystal X-ray diffraction analyses using the anomalous scattering of Cu Kα radiation. All of the isolated compounds were tested for activity against phytopathogenic fungi and nematodes. Compounds 2 and 3 showed antifungal activity and compound 2 showed weak nematicidal activity.
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spelling pubmed-63318822019-01-24 Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata Chen, Yan-Mei Yang, Yin-He Li, Xiao-Nian Zou, Cheng Zhao, Pei-Ji Molecules Article Two new tetranorlabdane diterpenoids, named botryosphaerins G (1) and H (2), were isolated from the solid fermentation products of Botryosphaeria sp. P483 along with seven known tetranorlabdane diterpenes (3–9). Their structures were elucidated by extensive analysis, including 1D and 2D nuclear magnetic resonance (NMR) spectroscopy, and high-resolution electrospray ionization mass spectrometry (HR-ESI-MS). Their absolute configuration was confirmed by single-crystal X-ray diffraction analyses using the anomalous scattering of Cu Kα radiation. All of the isolated compounds were tested for activity against phytopathogenic fungi and nematodes. Compounds 2 and 3 showed antifungal activity and compound 2 showed weak nematicidal activity. MDPI 2015-09-17 /pmc/articles/PMC6331882/ /pubmed/26393542 http://dx.doi.org/10.3390/molecules200916924 Text en © 2015 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Yan-Mei
Yang, Yin-He
Li, Xiao-Nian
Zou, Cheng
Zhao, Pei-Ji
Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata
title Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata
title_full Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata
title_fullStr Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata
title_full_unstemmed Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata
title_short Diterpenoids from the Endophytic Fungus Botryosphaeria sp. P483 of the Chinese Herbal Medicine Huperzia serrata
title_sort diterpenoids from the endophytic fungus botryosphaeria sp. p483 of the chinese herbal medicine huperzia serrata
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6331882/
https://www.ncbi.nlm.nih.gov/pubmed/26393542
http://dx.doi.org/10.3390/molecules200916924
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