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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...

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Autores principales: Yu, Ling-Ling, Li, Rong-Tao, Ai, Yuan-Bao, Liu, Wei, Deng, Zhang-Shuang, Zou, Zhong-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
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.
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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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