Cargando…
Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
The xishacorene natural products are structurally unique apolar diterpenoids that feature a bicyclo[3.3.1] framework. These secondary metabolites likely arise from the well-studied, structurally related diterpenoid fuscol. In this manuscript, we describe the conversion of fuscol to xishacorenes A, B...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761873/ https://www.ncbi.nlm.nih.gov/pubmed/31588327 http://dx.doi.org/10.1039/c9sc02572c |
_version_ | 1783454116055351296 |
---|---|
author | Rovira, Alexander R. Müller, Nicolas Deng, Weiwen Ndubaku, Chudi Sarpong, Richmond |
author_facet | Rovira, Alexander R. Müller, Nicolas Deng, Weiwen Ndubaku, Chudi Sarpong, Richmond |
author_sort | Rovira, Alexander R. |
collection | PubMed |
description | The xishacorene natural products are structurally unique apolar diterpenoids that feature a bicyclo[3.3.1] framework. These secondary metabolites likely arise from the well-studied, structurally related diterpenoid fuscol. In this manuscript, we describe the conversion of fuscol to xishacorenes A, B, and C, as well as a previously unreported congener, which we have named xishacorene D. In addition, we describe immunomodulatory activity studies of the xishacorenes, a structurally related analogue, and fuscol. These studies were aided by an accurate determination of the physical properties (e.g., molar extinction coefficient) of the highly apolar xishacorenes. |
format | Online Article Text |
id | pubmed-6761873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-67618732019-10-04 Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol Rovira, Alexander R. Müller, Nicolas Deng, Weiwen Ndubaku, Chudi Sarpong, Richmond Chem Sci Chemistry The xishacorene natural products are structurally unique apolar diterpenoids that feature a bicyclo[3.3.1] framework. These secondary metabolites likely arise from the well-studied, structurally related diterpenoid fuscol. In this manuscript, we describe the conversion of fuscol to xishacorenes A, B, and C, as well as a previously unreported congener, which we have named xishacorene D. In addition, we describe immunomodulatory activity studies of the xishacorenes, a structurally related analogue, and fuscol. These studies were aided by an accurate determination of the physical properties (e.g., molar extinction coefficient) of the highly apolar xishacorenes. Royal Society of Chemistry 2019-07-03 /pmc/articles/PMC6761873/ /pubmed/31588327 http://dx.doi.org/10.1039/c9sc02572c Text en This journal is © The Royal Society of Chemistry 2019 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Rovira, Alexander R. Müller, Nicolas Deng, Weiwen Ndubaku, Chudi Sarpong, Richmond Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol |
title | Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
|
title_full | Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
|
title_fullStr | Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
|
title_full_unstemmed | Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
|
title_short | Bio-inspired synthesis of xishacorenes A, B, and C, and a new congener from fuscol
|
title_sort | bio-inspired synthesis of xishacorenes a, b, and c, and a new congener from fuscol |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6761873/ https://www.ncbi.nlm.nih.gov/pubmed/31588327 http://dx.doi.org/10.1039/c9sc02572c |
work_keys_str_mv | AT roviraalexanderr bioinspiredsynthesisofxishacorenesabandcandanewcongenerfromfuscol AT mullernicolas bioinspiredsynthesisofxishacorenesabandcandanewcongenerfromfuscol AT dengweiwen bioinspiredsynthesisofxishacorenesabandcandanewcongenerfromfuscol AT ndubakuchudi bioinspiredsynthesisofxishacorenesabandcandanewcongenerfromfuscol AT sarpongrichmond bioinspiredsynthesisofxishacorenesabandcandanewcongenerfromfuscol |