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Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis

A structurally unprecedented prenylated indole alkaloid, beshanzuamide A (1), together with five known analogues (2–6) were isolated and identified from the endophytic fungus derived from the needles of the critically endangered conifer Abies beshanzuensis. The new structure was determined by extens...

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Autores principales: Zhu, Yuan-Xing, Ding, Wenxin, Hu, Jin-Feng, Xiong, Juan, Li, Jiyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985211/
https://www.ncbi.nlm.nih.gov/pubmed/35425024
http://dx.doi.org/10.1039/d2ra01578a
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author Zhu, Yuan-Xing
Ding, Wenxin
Hu, Jin-Feng
Xiong, Juan
Li, Jiyang
author_facet Zhu, Yuan-Xing
Ding, Wenxin
Hu, Jin-Feng
Xiong, Juan
Li, Jiyang
author_sort Zhu, Yuan-Xing
collection PubMed
description A structurally unprecedented prenylated indole alkaloid, beshanzuamide A (1), together with five known analogues (2–6) were isolated and identified from the endophytic fungus derived from the needles of the critically endangered conifer Abies beshanzuensis. The new structure was determined by extensive spectroscopic methods and quantum chemical calculations of NMR and electronic circular dichroism (ECD) data. Compound 1 features a unique N,O-spiroketal/δ-lactone motif connected to a pyranoindole-derived bicyclo[2.2.2]diazaoctane ring. A plausible biogenetic pathway for the assembly of 1 was proposed.
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spelling pubmed-89852112022-04-13 Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis Zhu, Yuan-Xing Ding, Wenxin Hu, Jin-Feng Xiong, Juan Li, Jiyang RSC Adv Chemistry A structurally unprecedented prenylated indole alkaloid, beshanzuamide A (1), together with five known analogues (2–6) were isolated and identified from the endophytic fungus derived from the needles of the critically endangered conifer Abies beshanzuensis. The new structure was determined by extensive spectroscopic methods and quantum chemical calculations of NMR and electronic circular dichroism (ECD) data. Compound 1 features a unique N,O-spiroketal/δ-lactone motif connected to a pyranoindole-derived bicyclo[2.2.2]diazaoctane ring. A plausible biogenetic pathway for the assembly of 1 was proposed. The Royal Society of Chemistry 2022-04-06 /pmc/articles/PMC8985211/ /pubmed/35425024 http://dx.doi.org/10.1039/d2ra01578a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zhu, Yuan-Xing
Ding, Wenxin
Hu, Jin-Feng
Xiong, Juan
Li, Jiyang
Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis
title Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis
title_full Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis
title_fullStr Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis
title_full_unstemmed Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis
title_short Beshanzuamide A, an unprecedented prenylated indole alkaloid produced by Aspergillus sp. Y-2 from the critically endangered conifer Abies beshanzuensis
title_sort beshanzuamide a, an unprecedented prenylated indole alkaloid produced by aspergillus sp. y-2 from the critically endangered conifer abies beshanzuensis
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985211/
https://www.ncbi.nlm.nih.gov/pubmed/35425024
http://dx.doi.org/10.1039/d2ra01578a
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