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Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS

In our continuous study for some African plants as a source for antitrypanosomally and cytotoxic active drugs, nine different plants belonging to the Crassulaceae family have been selected for the present study. Sedum sieboldii leaves extract showed an antitrypanosomal activity against Trypanosoma b...

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Autores principales: Hegazy, Mostafa M., Afifi, Wael M., Metwaly, Ahmed M., Radwan, Mohamed M., Abd-Elraouf, Muhamad, Mehany, Ahmed B. M., Ahmed, Eman, Enany, Shymaa, Ezzeldin, Shahd, Ibrahim, Adel E., El Deeb, Sami, Mostafa, Ahmad E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785725/
https://www.ncbi.nlm.nih.gov/pubmed/36557948
http://dx.doi.org/10.3390/molecules27248809
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author Hegazy, Mostafa M.
Afifi, Wael M.
Metwaly, Ahmed M.
Radwan, Mohamed M.
Abd-Elraouf, Muhamad
Mehany, Ahmed B. M.
Ahmed, Eman
Enany, Shymaa
Ezzeldin, Shahd
Ibrahim, Adel E.
El Deeb, Sami
Mostafa, Ahmad E.
author_facet Hegazy, Mostafa M.
Afifi, Wael M.
Metwaly, Ahmed M.
Radwan, Mohamed M.
Abd-Elraouf, Muhamad
Mehany, Ahmed B. M.
Ahmed, Eman
Enany, Shymaa
Ezzeldin, Shahd
Ibrahim, Adel E.
El Deeb, Sami
Mostafa, Ahmad E.
author_sort Hegazy, Mostafa M.
collection PubMed
description In our continuous study for some African plants as a source for antitrypanosomally and cytotoxic active drugs, nine different plants belonging to the Crassulaceae family have been selected for the present study. Sedum sieboldii leaves extract showed an antitrypanosomal activity against Trypanosoma brucei with an IC(50) value of 8.5 µg/mL. In addition, they have cytotoxic activities against (HCT-116), (HEPG-2) and (MCF-7), with IC(50) values of 28.18 ± 0.24, 22.05 ± 0.66, and 26.47 ± 0.85 µg/mL, respectively. Furthermore, the extract displayed inhibition against Topoisomerase-1 with an IC(50) value of 1.31 µg/mL. It showed the highest phenolics and flavonoids content among the other plants’ extracts. In order to identify the secondary metabolites which may be responsible for such activities, profiling of the polar secondary metabolites of S. sieboldii extract via Ultra-Performance Liquid Chromatography coupled to High-Resolution QTOF-MS operated in negative and positive ionization modes, which revealed the presence of 46 metabolites, including flavonoids, phenolic acids, anthocyanidins, coumarin, and other metabolites.
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spelling pubmed-97857252022-12-24 Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS Hegazy, Mostafa M. Afifi, Wael M. Metwaly, Ahmed M. Radwan, Mohamed M. Abd-Elraouf, Muhamad Mehany, Ahmed B. M. Ahmed, Eman Enany, Shymaa Ezzeldin, Shahd Ibrahim, Adel E. El Deeb, Sami Mostafa, Ahmad E. Molecules Article In our continuous study for some African plants as a source for antitrypanosomally and cytotoxic active drugs, nine different plants belonging to the Crassulaceae family have been selected for the present study. Sedum sieboldii leaves extract showed an antitrypanosomal activity against Trypanosoma brucei with an IC(50) value of 8.5 µg/mL. In addition, they have cytotoxic activities against (HCT-116), (HEPG-2) and (MCF-7), with IC(50) values of 28.18 ± 0.24, 22.05 ± 0.66, and 26.47 ± 0.85 µg/mL, respectively. Furthermore, the extract displayed inhibition against Topoisomerase-1 with an IC(50) value of 1.31 µg/mL. It showed the highest phenolics and flavonoids content among the other plants’ extracts. In order to identify the secondary metabolites which may be responsible for such activities, profiling of the polar secondary metabolites of S. sieboldii extract via Ultra-Performance Liquid Chromatography coupled to High-Resolution QTOF-MS operated in negative and positive ionization modes, which revealed the presence of 46 metabolites, including flavonoids, phenolic acids, anthocyanidins, coumarin, and other metabolites. MDPI 2022-12-12 /pmc/articles/PMC9785725/ /pubmed/36557948 http://dx.doi.org/10.3390/molecules27248809 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hegazy, Mostafa M.
Afifi, Wael M.
Metwaly, Ahmed M.
Radwan, Mohamed M.
Abd-Elraouf, Muhamad
Mehany, Ahmed B. M.
Ahmed, Eman
Enany, Shymaa
Ezzeldin, Shahd
Ibrahim, Adel E.
El Deeb, Sami
Mostafa, Ahmad E.
Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS
title Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS
title_full Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS
title_fullStr Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS
title_full_unstemmed Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS
title_short Antitrypanosomal, Antitopoisomerase-I, and Cytotoxic Biological Evaluation of Some African Plants Belonging to Crassulaceae; Chemical Profiling of Extract Using UHPLC/QTOF-MS/MS
title_sort antitrypanosomal, antitopoisomerase-i, and cytotoxic biological evaluation of some african plants belonging to crassulaceae; chemical profiling of extract using uhplc/qtof-ms/ms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9785725/
https://www.ncbi.nlm.nih.gov/pubmed/36557948
http://dx.doi.org/10.3390/molecules27248809
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