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Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung
HPLC-DAD-directed isolation and purification of the methanol extract of stems of Arcangelisia gusanlung H. S. Lo. led to the isolation of a new protoberberine alkaloid, gusanlung E (1), along with fourteen known derivatives 2–15, seven of which were obtained from the genus Arcangelisia for the first...
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/PMC6271463/ https://www.ncbi.nlm.nih.gov/pubmed/25178058 http://dx.doi.org/10.3390/molecules190913332 |
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author | Yu, Ling-Ling Li, Rong-Tao Ai, Yuan-Bao Liu, Wei Deng, Zhang-Shuang Zou, Zhong-Mei |
author_facet | Yu, Ling-Ling Li, Rong-Tao Ai, Yuan-Bao Liu, Wei Deng, Zhang-Shuang Zou, Zhong-Mei |
author_sort | Yu, Ling-Ling |
collection | PubMed |
description | HPLC-DAD-directed isolation and purification of the methanol extract of stems of Arcangelisia gusanlung H. S. Lo. led to the isolation of a new protoberberine alkaloid, gusanlung E (1), along with fourteen known derivatives 2–15, seven of which were obtained from the genus Arcangelisia for the first time. The structures and absolute stereochemistry of these compounds were elucidated on the basis of spectroscopic analyses, including 1D and 2D NMR, mass spectrometry, and CD analyses. Gusanlung E (1) expressed weak cytotoxic activity against the SGC 7901 cell line with an IC(50) value of 85.1 µM. |
format | Online Article Text |
id | pubmed-6271463 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62714632018-12-27 Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung Yu, Ling-Ling Li, Rong-Tao Ai, Yuan-Bao Liu, Wei Deng, Zhang-Shuang Zou, Zhong-Mei Molecules Article HPLC-DAD-directed isolation and purification of the methanol extract of stems of Arcangelisia gusanlung H. S. Lo. led to the isolation of a new protoberberine alkaloid, gusanlung E (1), along with fourteen known derivatives 2–15, seven of which were obtained from the genus Arcangelisia for the first time. The structures and absolute stereochemistry of these compounds were elucidated on the basis of spectroscopic analyses, including 1D and 2D NMR, mass spectrometry, and CD analyses. Gusanlung E (1) expressed weak cytotoxic activity against the SGC 7901 cell line with an IC(50) value of 85.1 µM. MDPI 2014-08-29 /pmc/articles/PMC6271463/ /pubmed/25178058 http://dx.doi.org/10.3390/molecules190913332 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 Yu, Ling-Ling Li, Rong-Tao Ai, Yuan-Bao Liu, Wei Deng, Zhang-Shuang Zou, Zhong-Mei Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung |
title | Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung |
title_full | Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung |
title_fullStr | Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung |
title_full_unstemmed | Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung |
title_short | Protoberberine Isoquinoline Alkaloids from Arcangelisia gusanlung |
title_sort | protoberberine isoquinoline alkaloids from arcangelisia gusanlung |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6271463/ https://www.ncbi.nlm.nih.gov/pubmed/25178058 http://dx.doi.org/10.3390/molecules190913332 |
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