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Germacranes and m-Menthane from Illicium lanceolatum
Three new germacrane sesquiterpenes and a new m-menthane monoterpene were isolated together with four known compounds from the pericarp of Illicium lanceolatum, an adulterant to star anise (Illicium verum). All compounds were isolated from Illicium plants for the first time. The absolute stereochemi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271484/ https://www.ncbi.nlm.nih.gov/pubmed/24714194 http://dx.doi.org/10.3390/molecules19044326 |
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author | Zhao, Ming Zhang, Xianming Wang, Yan Huang, Min Duan, Jin-Ao Gödecke, Tanja Szymulanska-Ramamurthy, Karina M. Yin, Zhiqi Che, Chun-Tao |
author_facet | Zhao, Ming Zhang, Xianming Wang, Yan Huang, Min Duan, Jin-Ao Gödecke, Tanja Szymulanska-Ramamurthy, Karina M. Yin, Zhiqi Che, Chun-Tao |
author_sort | Zhao, Ming |
collection | PubMed |
description | Three new germacrane sesquiterpenes and a new m-menthane monoterpene were isolated together with four known compounds from the pericarp of Illicium lanceolatum, an adulterant to star anise (Illicium verum). All compounds were isolated from Illicium plants for the first time. The absolute stereochemistry of all germacranes and m-menthane was established by a combination of NMR and the modified Mosher’s ester method. The biological activity was evaluated on SH-SY5Y neuroblastoma cell line. (1S,5R,7R)-1,5-Dihydroxygermacra-4(15),10(14),11(12)-triene (at 62.5 µM) and (1R,5R,7R)-1,5-dihydroxygermacra-4(15),10(14),11(12)-triene (at 15.6 µM) promoted the proliferation of SH-SY5Y by 36.2% and 45.8%, respectively, after 48 h incubation, indicating potential neurotrophic activity. |
format | Online Article Text |
id | pubmed-6271484 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62714842019-01-02 Germacranes and m-Menthane from Illicium lanceolatum Zhao, Ming Zhang, Xianming Wang, Yan Huang, Min Duan, Jin-Ao Gödecke, Tanja Szymulanska-Ramamurthy, Karina M. Yin, Zhiqi Che, Chun-Tao Molecules Article Three new germacrane sesquiterpenes and a new m-menthane monoterpene were isolated together with four known compounds from the pericarp of Illicium lanceolatum, an adulterant to star anise (Illicium verum). All compounds were isolated from Illicium plants for the first time. The absolute stereochemistry of all germacranes and m-menthane was established by a combination of NMR and the modified Mosher’s ester method. The biological activity was evaluated on SH-SY5Y neuroblastoma cell line. (1S,5R,7R)-1,5-Dihydroxygermacra-4(15),10(14),11(12)-triene (at 62.5 µM) and (1R,5R,7R)-1,5-dihydroxygermacra-4(15),10(14),11(12)-triene (at 15.6 µM) promoted the proliferation of SH-SY5Y by 36.2% and 45.8%, respectively, after 48 h incubation, indicating potential neurotrophic activity. MDPI 2014-04-04 /pmc/articles/PMC6271484/ /pubmed/24714194 http://dx.doi.org/10.3390/molecules19044326 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/3.0/). |
spellingShingle | Article Zhao, Ming Zhang, Xianming Wang, Yan Huang, Min Duan, Jin-Ao Gödecke, Tanja Szymulanska-Ramamurthy, Karina M. Yin, Zhiqi Che, Chun-Tao Germacranes and m-Menthane from Illicium lanceolatum |
title | Germacranes and m-Menthane from Illicium lanceolatum |
title_full | Germacranes and m-Menthane from Illicium lanceolatum |
title_fullStr | Germacranes and m-Menthane from Illicium lanceolatum |
title_full_unstemmed | Germacranes and m-Menthane from Illicium lanceolatum |
title_short | Germacranes and m-Menthane from Illicium lanceolatum |
title_sort | germacranes and m-menthane from illicium lanceolatum |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271484/ https://www.ncbi.nlm.nih.gov/pubmed/24714194 http://dx.doi.org/10.3390/molecules19044326 |
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