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Alkylamides of Acmella oleracea
Phytochemical investigation of the flowers of Acmella oleracea had resulted in the isolation of one new alkylamide, (2E,5Z)-N-isobutylundeca-2,5-diene-8,10-diynamide (1), together with four known analogues (2−5). The structures of these compounds were determined by the interpretation of spectroscopi...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272129/ https://www.ncbi.nlm.nih.gov/pubmed/25913934 http://dx.doi.org/10.3390/molecules20046970 |
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author | Cheng, Yuan-Bin Liu, Rosa Huang Ho, Meng-Chi Wu, Tung-Ying Chen, Ching-Yeu Lo, I-Wen Hou, Ming-Feng Yuan, Shyng-Shiou Wu, Yang-Chang Chang, Fang-Rong |
author_facet | Cheng, Yuan-Bin Liu, Rosa Huang Ho, Meng-Chi Wu, Tung-Ying Chen, Ching-Yeu Lo, I-Wen Hou, Ming-Feng Yuan, Shyng-Shiou Wu, Yang-Chang Chang, Fang-Rong |
author_sort | Cheng, Yuan-Bin |
collection | PubMed |
description | Phytochemical investigation of the flowers of Acmella oleracea had resulted in the isolation of one new alkylamide, (2E,5Z)-N-isobutylundeca-2,5-diene-8,10-diynamide (1), together with four known analogues (2−5). The structures of these compounds were determined by the interpretation of spectroscopic methods, especially NMR technologies (COSY, HSQC, HMBC, and NOESY). In addition, a convenient method for concentrating the alkylamide-rich fraction and analyzing fingerprint profile of A. oleracea was established. |
format | Online Article Text |
id | pubmed-6272129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62721292018-12-03 Alkylamides of Acmella oleracea Cheng, Yuan-Bin Liu, Rosa Huang Ho, Meng-Chi Wu, Tung-Ying Chen, Ching-Yeu Lo, I-Wen Hou, Ming-Feng Yuan, Shyng-Shiou Wu, Yang-Chang Chang, Fang-Rong Molecules Article Phytochemical investigation of the flowers of Acmella oleracea had resulted in the isolation of one new alkylamide, (2E,5Z)-N-isobutylundeca-2,5-diene-8,10-diynamide (1), together with four known analogues (2−5). The structures of these compounds were determined by the interpretation of spectroscopic methods, especially NMR technologies (COSY, HSQC, HMBC, and NOESY). In addition, a convenient method for concentrating the alkylamide-rich fraction and analyzing fingerprint profile of A. oleracea was established. MDPI 2015-04-16 /pmc/articles/PMC6272129/ /pubmed/25913934 http://dx.doi.org/10.3390/molecules20046970 Text en © 2015 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 Cheng, Yuan-Bin Liu, Rosa Huang Ho, Meng-Chi Wu, Tung-Ying Chen, Ching-Yeu Lo, I-Wen Hou, Ming-Feng Yuan, Shyng-Shiou Wu, Yang-Chang Chang, Fang-Rong Alkylamides of Acmella oleracea |
title | Alkylamides of Acmella oleracea |
title_full | Alkylamides of Acmella oleracea |
title_fullStr | Alkylamides of Acmella oleracea |
title_full_unstemmed | Alkylamides of Acmella oleracea |
title_short | Alkylamides of Acmella oleracea |
title_sort | alkylamides of acmella oleracea |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272129/ https://www.ncbi.nlm.nih.gov/pubmed/25913934 http://dx.doi.org/10.3390/molecules20046970 |
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