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Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii
Three new ent-kauranoids, isorosthornins A-C (1–3), and a new natural product, dihydroponicidin (4), together with five known ones were isolated from the aerial parts of Isodon rosthornii. The structures were determined by means of extensive spectroscopic analysis. All diterpenoids isolated were eva...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131646/ http://dx.doi.org/10.1007/s13659-011-0031-7 |
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author | Zhan, Rui Du, Xue Su, Jia Li, Xiao-Nian Wang, Wei-Guang Liang, Cheng-Qin Yang, Jian-Hong Li, Yan Pu, Jian-Xin Sun, Han-Dong |
author_facet | Zhan, Rui Du, Xue Su, Jia Li, Xiao-Nian Wang, Wei-Guang Liang, Cheng-Qin Yang, Jian-Hong Li, Yan Pu, Jian-Xin Sun, Han-Dong |
author_sort | Zhan, Rui |
collection | PubMed |
description | Three new ent-kauranoids, isorosthornins A-C (1–3), and a new natural product, dihydroponicidin (4), together with five known ones were isolated from the aerial parts of Isodon rosthornii. The structures were determined by means of extensive spectroscopic analysis. All diterpenoids isolated were evaluated for their cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, and SW480 cell lines, and compounds 5 and 7 showed significant inhibitory effects on all cell lines. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-011-0031-7 and is accessible for authorized users. |
format | Online Article Text |
id | pubmed-4131646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-41316462014-08-20 Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii Zhan, Rui Du, Xue Su, Jia Li, Xiao-Nian Wang, Wei-Guang Liang, Cheng-Qin Yang, Jian-Hong Li, Yan Pu, Jian-Xin Sun, Han-Dong Nat Prod Bioprospect Regular Article Three new ent-kauranoids, isorosthornins A-C (1–3), and a new natural product, dihydroponicidin (4), together with five known ones were isolated from the aerial parts of Isodon rosthornii. The structures were determined by means of extensive spectroscopic analysis. All diterpenoids isolated were evaluated for their cytotoxicity against HL-60, SMMC-7721, A-549, MCF-7, and SW480 cell lines, and compounds 5 and 7 showed significant inhibitory effects on all cell lines. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: Supplementary material is available for this article at 10.1007/s13659-011-0031-7 and is accessible for authorized users. Springer Berlin Heidelberg 2011-12-12 /pmc/articles/PMC4131646/ http://dx.doi.org/10.1007/s13659-011-0031-7 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by/4.0/ This article is published under license to BioMed Central Ltd. Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Regular Article Zhan, Rui Du, Xue Su, Jia Li, Xiao-Nian Wang, Wei-Guang Liang, Cheng-Qin Yang, Jian-Hong Li, Yan Pu, Jian-Xin Sun, Han-Dong Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii |
title | Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii |
title_full | Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii |
title_fullStr | Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii |
title_full_unstemmed | Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii |
title_short | Isorosthornins A-C, new ent-kaurane diterpenoids from Isodon rosthornii |
title_sort | isorosthornins a-c, new ent-kaurane diterpenoids from isodon rosthornii |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4131646/ http://dx.doi.org/10.1007/s13659-011-0031-7 |
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