Cargando…
Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids
The antiproliferative activity of a set of seven natural Amaryllidaceae alkaloids and 32 derivatives against four cancer cell lines (A2780, SW1573, T47-D and WiDr) was determined. The best antiproliferative activities were achieved with alkaloids derived from pancracine (2), haemanthamine (6) and ha...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332398/ https://www.ncbi.nlm.nih.gov/pubmed/26263960 http://dx.doi.org/10.3390/molecules200813854 |
_version_ | 1783387341665075200 |
---|---|
author | Cedrón, Juan C. Ravelo, Ángel G. León, Leticia G. Padrón, José M. Estévez-Braun, Ana |
author_facet | Cedrón, Juan C. Ravelo, Ángel G. León, Leticia G. Padrón, José M. Estévez-Braun, Ana |
author_sort | Cedrón, Juan C. |
collection | PubMed |
description | The antiproliferative activity of a set of seven natural Amaryllidaceae alkaloids and 32 derivatives against four cancer cell lines (A2780, SW1573, T47-D and WiDr) was determined. The best antiproliferative activities were achieved with alkaloids derived from pancracine (2), haemanthamine (6) and haemantidine (7). For each skeleton, some structure-activity relationships were outlined. |
format | Online Article Text |
id | pubmed-6332398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63323982019-01-24 Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids Cedrón, Juan C. Ravelo, Ángel G. León, Leticia G. Padrón, José M. Estévez-Braun, Ana Molecules Article The antiproliferative activity of a set of seven natural Amaryllidaceae alkaloids and 32 derivatives against four cancer cell lines (A2780, SW1573, T47-D and WiDr) was determined. The best antiproliferative activities were achieved with alkaloids derived from pancracine (2), haemanthamine (6) and haemantidine (7). For each skeleton, some structure-activity relationships were outlined. MDPI 2015-07-30 /pmc/articles/PMC6332398/ /pubmed/26263960 http://dx.doi.org/10.3390/molecules200813854 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 Cedrón, Juan C. Ravelo, Ángel G. León, Leticia G. Padrón, José M. Estévez-Braun, Ana Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids |
title | Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids |
title_full | Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids |
title_fullStr | Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids |
title_full_unstemmed | Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids |
title_short | Antiproliferative and Structure Activity Relationships of Amaryllidaceae Alkaloids |
title_sort | antiproliferative and structure activity relationships of amaryllidaceae alkaloids |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6332398/ https://www.ncbi.nlm.nih.gov/pubmed/26263960 http://dx.doi.org/10.3390/molecules200813854 |
work_keys_str_mv | AT cedronjuanc antiproliferativeandstructureactivityrelationshipsofamaryllidaceaealkaloids AT raveloangelg antiproliferativeandstructureactivityrelationshipsofamaryllidaceaealkaloids AT leonleticiag antiproliferativeandstructureactivityrelationshipsofamaryllidaceaealkaloids AT padronjosem antiproliferativeandstructureactivityrelationshipsofamaryllidaceaealkaloids AT estevezbraunana antiproliferativeandstructureactivityrelationshipsofamaryllidaceaealkaloids |