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Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis (†)
A new indole alkaloid, naucline (1) together with four known alkaloids, angustine (2), angustidine (3), nauclefine (4) and naucletine (5), were isolated from the bark of Nauclea officinalis. The structures of all isolated compounds were elucidated with various spectroscopic methods such as 1D- and 2...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268295/ https://www.ncbi.nlm.nih.gov/pubmed/22469596 http://dx.doi.org/10.3390/molecules17044028 |
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author | Liew, Sook Yee Mukhtar, Mat Ropi Hadi, A. Hamid A. Awang, Khalijah Mustafa, Mohd Rais Zaima, Kazumasa Morita, Hiroshi Litaudon, Marc |
author_facet | Liew, Sook Yee Mukhtar, Mat Ropi Hadi, A. Hamid A. Awang, Khalijah Mustafa, Mohd Rais Zaima, Kazumasa Morita, Hiroshi Litaudon, Marc |
author_sort | Liew, Sook Yee |
collection | PubMed |
description | A new indole alkaloid, naucline (1) together with four known alkaloids, angustine (2), angustidine (3), nauclefine (4) and naucletine (5), were isolated from the bark of Nauclea officinalis. The structures of all isolated compounds were elucidated with various spectroscopic methods such as 1D- and 2D- NMR, IR, UV and LCMS-IT-TOF. In addition to that of alkaloid 1, the complete (13)C-NMR data of naucletine (5) were also reported. Naucline (1) showed a moderate vasorelaxant activity (90% relaxation at 1 × 10(−5) M) whereas, angustine (2), nauclefine (4), and naucletine (5) showed potent vasorelaxant activity (more than 90% relaxation at 1 × 10(−5) M) on an isolated rat aorta. |
format | Online Article Text |
id | pubmed-6268295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62682952018-12-11 Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis (†) Liew, Sook Yee Mukhtar, Mat Ropi Hadi, A. Hamid A. Awang, Khalijah Mustafa, Mohd Rais Zaima, Kazumasa Morita, Hiroshi Litaudon, Marc Molecules Article A new indole alkaloid, naucline (1) together with four known alkaloids, angustine (2), angustidine (3), nauclefine (4) and naucletine (5), were isolated from the bark of Nauclea officinalis. The structures of all isolated compounds were elucidated with various spectroscopic methods such as 1D- and 2D- NMR, IR, UV and LCMS-IT-TOF. In addition to that of alkaloid 1, the complete (13)C-NMR data of naucletine (5) were also reported. Naucline (1) showed a moderate vasorelaxant activity (90% relaxation at 1 × 10(−5) M) whereas, angustine (2), nauclefine (4), and naucletine (5) showed potent vasorelaxant activity (more than 90% relaxation at 1 × 10(−5) M) on an isolated rat aorta. MDPI 2012-04-02 /pmc/articles/PMC6268295/ /pubmed/22469596 http://dx.doi.org/10.3390/molecules17044028 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ 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 Liew, Sook Yee Mukhtar, Mat Ropi Hadi, A. Hamid A. Awang, Khalijah Mustafa, Mohd Rais Zaima, Kazumasa Morita, Hiroshi Litaudon, Marc Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis (†) |
title | Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis
(†) |
title_full | Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis
(†) |
title_fullStr | Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis
(†) |
title_full_unstemmed | Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis
(†) |
title_short | Naucline, a New Indole Alkaloid from the Bark of Nauclea officinalis
(†) |
title_sort | naucline, a new indole alkaloid from the bark of nauclea officinalis
(†) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268295/ https://www.ncbi.nlm.nih.gov/pubmed/22469596 http://dx.doi.org/10.3390/molecules17044028 |
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