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In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.

Chromatographic separation of the n-hexane extract of the aerial part of Plectranthus barbatus led to the isolation of five abietane-type diterpenes: dehydroabietane (1); 5,6-didehydro-7-hydroxy-taxodone (2); taxodione (3); 20-deoxocarnosol (4) and 6α,11,12,-trihydroxy-7β,20-epoxy-8,11,13-abietatrie...

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Autores principales: Mothana, Ramzi A., Al-Said, Mansour S., Al-Musayeib, Nawal M., El Gamal, Ali A., Al-Massarani, Shaza M., Al-Rehaily, Adnan J., Abdulkader, Majed, Maes, Louis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057736/
https://www.ncbi.nlm.nih.gov/pubmed/24823881
http://dx.doi.org/10.3390/ijms15058360
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author Mothana, Ramzi A.
Al-Said, Mansour S.
Al-Musayeib, Nawal M.
El Gamal, Ali A.
Al-Massarani, Shaza M.
Al-Rehaily, Adnan J.
Abdulkader, Majed
Maes, Louis
author_facet Mothana, Ramzi A.
Al-Said, Mansour S.
Al-Musayeib, Nawal M.
El Gamal, Ali A.
Al-Massarani, Shaza M.
Al-Rehaily, Adnan J.
Abdulkader, Majed
Maes, Louis
author_sort Mothana, Ramzi A.
collection PubMed
description Chromatographic separation of the n-hexane extract of the aerial part of Plectranthus barbatus led to the isolation of five abietane-type diterpenes: dehydroabietane (1); 5,6-didehydro-7-hydroxy-taxodone (2); taxodione (3); 20-deoxocarnosol (4) and 6α,11,12,-trihydroxy-7β,20-epoxy-8,11,13-abietatriene (5). The structures were determined using spectroscopic methods including one- and two-dimensional NMR methods. Compounds (1)–(3) and (5) are isolated here for the first time from the genus Plectranthus. The isolated abietane-type diterpenes tested in vitro for their antiprotozoal activity against erythrocytic schizonts of Plasmodium falciparum, intracellular amastigotes of Leishmania infantum and Trypanosoma cruzi and free trypomastigotes of T. brucei. Cytotoxicity was determined against fibroblast cell line MRC-5. Compound (2) 5,6-didehydro-7-hydroxy-taxodone showed remarkable activity with acceptable selectivity against P. falciparum (IC(50) 9.2 μM, SI 10.4) and T. brucei (IC(50) 1.9 μM, SI 50.5). Compounds (3)–(5) exhibited non-specific antiprotozoal activity due to high cytotoxicity. Compound (1) dehydroabietane showed no antiprotozoal potential.
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spelling pubmed-40577362014-06-16 In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr. Mothana, Ramzi A. Al-Said, Mansour S. Al-Musayeib, Nawal M. El Gamal, Ali A. Al-Massarani, Shaza M. Al-Rehaily, Adnan J. Abdulkader, Majed Maes, Louis Int J Mol Sci Article Chromatographic separation of the n-hexane extract of the aerial part of Plectranthus barbatus led to the isolation of five abietane-type diterpenes: dehydroabietane (1); 5,6-didehydro-7-hydroxy-taxodone (2); taxodione (3); 20-deoxocarnosol (4) and 6α,11,12,-trihydroxy-7β,20-epoxy-8,11,13-abietatriene (5). The structures were determined using spectroscopic methods including one- and two-dimensional NMR methods. Compounds (1)–(3) and (5) are isolated here for the first time from the genus Plectranthus. The isolated abietane-type diterpenes tested in vitro for their antiprotozoal activity against erythrocytic schizonts of Plasmodium falciparum, intracellular amastigotes of Leishmania infantum and Trypanosoma cruzi and free trypomastigotes of T. brucei. Cytotoxicity was determined against fibroblast cell line MRC-5. Compound (2) 5,6-didehydro-7-hydroxy-taxodone showed remarkable activity with acceptable selectivity against P. falciparum (IC(50) 9.2 μM, SI 10.4) and T. brucei (IC(50) 1.9 μM, SI 50.5). Compounds (3)–(5) exhibited non-specific antiprotozoal activity due to high cytotoxicity. Compound (1) dehydroabietane showed no antiprotozoal potential. Molecular Diversity Preservation International (MDPI) 2014-05-12 /pmc/articles/PMC4057736/ /pubmed/24823881 http://dx.doi.org/10.3390/ijms15058360 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ 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
Mothana, Ramzi A.
Al-Said, Mansour S.
Al-Musayeib, Nawal M.
El Gamal, Ali A.
Al-Massarani, Shaza M.
Al-Rehaily, Adnan J.
Abdulkader, Majed
Maes, Louis
In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
title In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
title_full In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
title_fullStr In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
title_full_unstemmed In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
title_short In Vitro Antiprotozoal Activity of Abietane Diterpenoids Isolated from Plectranthus barbatus Andr.
title_sort in vitro antiprotozoal activity of abietane diterpenoids isolated from plectranthus barbatus andr.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057736/
https://www.ncbi.nlm.nih.gov/pubmed/24823881
http://dx.doi.org/10.3390/ijms15058360
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