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A New Hydroxychavicol Dimer from the Roots of Piper betle
A new hydroxychavicol dimer, 2-(γ'-hydroxychavicol)-hydroxychavicol (1), was isolated from the roots of Piper betle Linn. along with five known compounds, hydroxychavicol (2), aristololactam A II (3), aristololactam B II (4), piperolactam A (5) and cepharadione A (6). The structures of these is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270560/ https://www.ncbi.nlm.nih.gov/pubmed/23442932 http://dx.doi.org/10.3390/molecules18032563 |
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author | Lin, Chwan-Fwu Hwang, Tsong-Long Chien, Chun-Chien Tu, Huei-Yu Lay, Horng-Liang |
author_facet | Lin, Chwan-Fwu Hwang, Tsong-Long Chien, Chun-Chien Tu, Huei-Yu Lay, Horng-Liang |
author_sort | Lin, Chwan-Fwu |
collection | PubMed |
description | A new hydroxychavicol dimer, 2-(γ'-hydroxychavicol)-hydroxychavicol (1), was isolated from the roots of Piper betle Linn. along with five known compounds, hydroxychavicol (2), aristololactam A II (3), aristololactam B II (4), piperolactam A (5) and cepharadione A (6). The structures of these isolated compounds were elucidated by spectroscopic methods. Compounds 1 and 2 exhibited inhibitory effects on the generation of superoxide anion and the release of elastase by human neutrophils. |
format | Online Article Text |
id | pubmed-6270560 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62705602018-12-20 A New Hydroxychavicol Dimer from the Roots of Piper betle Lin, Chwan-Fwu Hwang, Tsong-Long Chien, Chun-Chien Tu, Huei-Yu Lay, Horng-Liang Molecules Article A new hydroxychavicol dimer, 2-(γ'-hydroxychavicol)-hydroxychavicol (1), was isolated from the roots of Piper betle Linn. along with five known compounds, hydroxychavicol (2), aristololactam A II (3), aristololactam B II (4), piperolactam A (5) and cepharadione A (6). The structures of these isolated compounds were elucidated by spectroscopic methods. Compounds 1 and 2 exhibited inhibitory effects on the generation of superoxide anion and the release of elastase by human neutrophils. MDPI 2013-02-26 /pmc/articles/PMC6270560/ /pubmed/23442932 http://dx.doi.org/10.3390/molecules18032563 Text en © 2013 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 Lin, Chwan-Fwu Hwang, Tsong-Long Chien, Chun-Chien Tu, Huei-Yu Lay, Horng-Liang A New Hydroxychavicol Dimer from the Roots of Piper betle |
title | A New Hydroxychavicol Dimer from the Roots of Piper betle |
title_full | A New Hydroxychavicol Dimer from the Roots of Piper betle |
title_fullStr | A New Hydroxychavicol Dimer from the Roots of Piper betle |
title_full_unstemmed | A New Hydroxychavicol Dimer from the Roots of Piper betle |
title_short | A New Hydroxychavicol Dimer from the Roots of Piper betle |
title_sort | new hydroxychavicol dimer from the roots of piper betle |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270560/ https://www.ncbi.nlm.nih.gov/pubmed/23442932 http://dx.doi.org/10.3390/molecules18032563 |
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