Cargando…

Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity

Objectives: The current study aimed at exploring the secondary metabolites content of Erythrina crista-galli aqueous methanol extract and assessing its phytoestrogenic and cytoprotective activities. Methods: Isolation of the compounds was carried out using conventional chromatographic techniques. Th...

Descripción completa

Detalles Bibliográficos
Autores principales: Ashmawy, Naglaa S., Ashour, Mohamed L., Wink, Michael, El-Shazly, Mohamed, Chang, Fang-Rong, Swilam, Noha, Abdel-Naim, Ashraf B., Ayoub, Nahla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274393/
https://www.ncbi.nlm.nih.gov/pubmed/27271580
http://dx.doi.org/10.3390/molecules21060726
_version_ 1783377607713095680
author Ashmawy, Naglaa S.
Ashour, Mohamed L.
Wink, Michael
El-Shazly, Mohamed
Chang, Fang-Rong
Swilam, Noha
Abdel-Naim, Ashraf B.
Ayoub, Nahla
author_facet Ashmawy, Naglaa S.
Ashour, Mohamed L.
Wink, Michael
El-Shazly, Mohamed
Chang, Fang-Rong
Swilam, Noha
Abdel-Naim, Ashraf B.
Ayoub, Nahla
author_sort Ashmawy, Naglaa S.
collection PubMed
description Objectives: The current study aimed at exploring the secondary metabolites content of Erythrina crista-galli aqueous methanol extract and assessing its phytoestrogenic and cytoprotective activities. Methods: Isolation of the compounds was carried out using conventional chromatographic techniques. The structures of the isolated compounds were elucidated based on the UV, NMR spectral data along with their mass-spectrometric analyses. The phytoestrogenic activity was evaluated in-silico and in vitro using the Arabidopsis thaliana pER8: GUS reporter assay and the proliferation-enhancing activity of MCF-7 cells. Key findings: Phytochemical investigation of E. crista-galli aqueous methanol extract resulted in the isolation and identification of five flavonoids. The plant extract and its fractions showed significant estrogenic activities compared to controls. Conclusion: Five flavonoids were identified from E. crista-galli aqueous methanol extract. To the best of our knowledge, among these flavonoids, apigenin-7-O-rhamnosyl-6-C-glucoside was isolated for the first time from nature. Moreover, luteolin-6-C-glucoside was isolated for the first time from this plant. The plant revealed promising phytoestrogenic activities. This gives rationale to some of its pharmacological properties and suggests additional phytoestrogenic effects, which have not been reported yet.
format Online
Article
Text
id pubmed-6274393
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62743932018-12-28 Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity Ashmawy, Naglaa S. Ashour, Mohamed L. Wink, Michael El-Shazly, Mohamed Chang, Fang-Rong Swilam, Noha Abdel-Naim, Ashraf B. Ayoub, Nahla Molecules Article Objectives: The current study aimed at exploring the secondary metabolites content of Erythrina crista-galli aqueous methanol extract and assessing its phytoestrogenic and cytoprotective activities. Methods: Isolation of the compounds was carried out using conventional chromatographic techniques. The structures of the isolated compounds were elucidated based on the UV, NMR spectral data along with their mass-spectrometric analyses. The phytoestrogenic activity was evaluated in-silico and in vitro using the Arabidopsis thaliana pER8: GUS reporter assay and the proliferation-enhancing activity of MCF-7 cells. Key findings: Phytochemical investigation of E. crista-galli aqueous methanol extract resulted in the isolation and identification of five flavonoids. The plant extract and its fractions showed significant estrogenic activities compared to controls. Conclusion: Five flavonoids were identified from E. crista-galli aqueous methanol extract. To the best of our knowledge, among these flavonoids, apigenin-7-O-rhamnosyl-6-C-glucoside was isolated for the first time from nature. Moreover, luteolin-6-C-glucoside was isolated for the first time from this plant. The plant revealed promising phytoestrogenic activities. This gives rationale to some of its pharmacological properties and suggests additional phytoestrogenic effects, which have not been reported yet. MDPI 2016-06-03 /pmc/articles/PMC6274393/ /pubmed/27271580 http://dx.doi.org/10.3390/molecules21060726 Text en © 2016 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 (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ashmawy, Naglaa S.
Ashour, Mohamed L.
Wink, Michael
El-Shazly, Mohamed
Chang, Fang-Rong
Swilam, Noha
Abdel-Naim, Ashraf B.
Ayoub, Nahla
Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity
title Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity
title_full Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity
title_fullStr Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity
title_full_unstemmed Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity
title_short Polyphenols from Erythrina crista-galli: Structures, Molecular Docking and Phytoestrogenic Activity
title_sort polyphenols from erythrina crista-galli: structures, molecular docking and phytoestrogenic activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274393/
https://www.ncbi.nlm.nih.gov/pubmed/27271580
http://dx.doi.org/10.3390/molecules21060726
work_keys_str_mv AT ashmawynaglaas polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT ashourmohamedl polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT winkmichael polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT elshazlymohamed polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT changfangrong polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT swilamnoha polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT abdelnaimashrafb polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity
AT ayoubnahla polyphenolsfromerythrinacristagallistructuresmoleculardockingandphytoestrogenicactivity