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Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus

Six sesquiterpenoids 1–6, including two new ones, an ent-daucane-type sesquiterpenoid, asperaculane A (1), and a nordaucane one, asperaculane B (2), and four known nordaucane derivatives, aculenes A–D 3–6, together with the known secalonic acid D (7), were isolated from a fermentation culture of the...

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Detalles Bibliográficos
Autores principales: Gao, Yu-Qi, Guo, Chun-Jun, Zhang, Qiang, Zhou, Wen-Ming, Wang, Clay C. C., Gao, Jin-Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272214/
https://www.ncbi.nlm.nih.gov/pubmed/25547729
http://dx.doi.org/10.3390/molecules20010325
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author Gao, Yu-Qi
Guo, Chun-Jun
Zhang, Qiang
Zhou, Wen-Ming
Wang, Clay C. C.
Gao, Jin-Ming
author_facet Gao, Yu-Qi
Guo, Chun-Jun
Zhang, Qiang
Zhou, Wen-Ming
Wang, Clay C. C.
Gao, Jin-Ming
author_sort Gao, Yu-Qi
collection PubMed
description Six sesquiterpenoids 1–6, including two new ones, an ent-daucane-type sesquiterpenoid, asperaculane A (1), and a nordaucane one, asperaculane B (2), and four known nordaucane derivatives, aculenes A–D 3–6, together with the known secalonic acid D (7), were isolated from a fermentation culture of the fungus Aspergillus aculeatus. Their structures and absolute configurations were established by analyses of their spectroscopic data, including 1D and 2D-NMR spectra, HR-ESIMS, electronic circular dichroism (ECD) data, and quantum chemical calculations. These metabolites were evaluated for in vitro cytotoxic activity against two cell lines, human cancer cell lines (HeLa) and one normal hamster cell line (CHO).
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spelling pubmed-62722142018-12-28 Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus Gao, Yu-Qi Guo, Chun-Jun Zhang, Qiang Zhou, Wen-Ming Wang, Clay C. C. Gao, Jin-Ming Molecules Article Six sesquiterpenoids 1–6, including two new ones, an ent-daucane-type sesquiterpenoid, asperaculane A (1), and a nordaucane one, asperaculane B (2), and four known nordaucane derivatives, aculenes A–D 3–6, together with the known secalonic acid D (7), were isolated from a fermentation culture of the fungus Aspergillus aculeatus. Their structures and absolute configurations were established by analyses of their spectroscopic data, including 1D and 2D-NMR spectra, HR-ESIMS, electronic circular dichroism (ECD) data, and quantum chemical calculations. These metabolites were evaluated for in vitro cytotoxic activity against two cell lines, human cancer cell lines (HeLa) and one normal hamster cell line (CHO). MDPI 2014-12-25 /pmc/articles/PMC6272214/ /pubmed/25547729 http://dx.doi.org/10.3390/molecules20010325 Text en © 2014 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
Gao, Yu-Qi
Guo, Chun-Jun
Zhang, Qiang
Zhou, Wen-Ming
Wang, Clay C. C.
Gao, Jin-Ming
Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus
title Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus
title_full Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus
title_fullStr Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus
title_full_unstemmed Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus
title_short Asperaculanes A and B, Two Sesquiterpenoids from the Fungus Aspergillus aculeatus
title_sort asperaculanes a and b, two sesquiterpenoids from the fungus aspergillus aculeatus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272214/
https://www.ncbi.nlm.nih.gov/pubmed/25547729
http://dx.doi.org/10.3390/molecules20010325
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