Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1783377103959359488 |
---|---|
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). |
format | Online Article Text |
id | pubmed-6272214 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT gaoyuqi asperaculanesaandbtwosesquiterpenoidsfromthefungusaspergillusaculeatus AT guochunjun asperaculanesaandbtwosesquiterpenoidsfromthefungusaspergillusaculeatus AT zhangqiang asperaculanesaandbtwosesquiterpenoidsfromthefungusaspergillusaculeatus AT zhouwenming asperaculanesaandbtwosesquiterpenoidsfromthefungusaspergillusaculeatus AT wangclaycc asperaculanesaandbtwosesquiterpenoidsfromthefungusaspergillusaculeatus AT gaojinming asperaculanesaandbtwosesquiterpenoidsfromthefungusaspergillusaculeatus |