Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar

Objective: To isolate and characterize the cytotoxic compounds from Diospyros quercina (Baill.) G.E. Schatz & Lowry (Ebenaceae). Methods: An ethno-botanical survey was conducted in the south of Madagascar from July to August 2010. Bio-guided fractionation assay was carried out on the root bark o...

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Published in:Asian Pacific Journal of Tropical Biomedicine
Main Authors: Fatiany Pierre Ruphin, Robijaona Baholy, Randrianarivo Emmanuel, Raharisololalao Amelie, Marie-Therese Martin, Ngbolua Koto–te-Nyiwa
Format: Article in Journal/Newspaper
Language:English
Published: Wolters Kluwer Medknow Publications 2014
Subjects:
Online Access:https://doi.org/10.1016/S2221-1691(14)60227-6
https://doaj.org/article/8f76845b11e34768864f55c7cd0ba6f7
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spelling ftdoajarticles:oai:doaj.org/article:8f76845b11e34768864f55c7cd0ba6f7 2023-05-15T15:11:16+02:00 Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar Fatiany Pierre Ruphin Robijaona Baholy Randrianarivo Emmanuel Raharisololalao Amelie Marie-Therese Martin Ngbolua Koto–te-Nyiwa 2014-03-01T00:00:00Z https://doi.org/10.1016/S2221-1691(14)60227-6 https://doaj.org/article/8f76845b11e34768864f55c7cd0ba6f7 EN eng Wolters Kluwer Medknow Publications http://www.sciencedirect.com/science/article/pii/S222116911530188X https://doaj.org/toc/2221-1691 2221-1691 doi:10.1016/S2221-1691(14)60227-6 https://doaj.org/article/8f76845b11e34768864f55c7cd0ba6f7 Asian Pacific Journal of Tropical Biomedicine, Vol 4, Iss 3, Pp 169-175 (2014) Diospyros quercinia Cytotoxic activities Isodiospyrin 6′-Ethoxy-1′ 3′-dihydroxy-4 6-dimethyl-1,2′-binaphthyl-2,5′,8,8′tetraones (E)-5,6-Dimethyl-2-(2-methyl-3-(prop-1-enyl) phenyl)-2H-Chromene Madagascar Arctic medicine. Tropical medicine RC955-962 Biology (General) QH301-705.5 article 2014 ftdoajarticles https://doi.org/10.1016/S2221-1691(14)60227-6 2022-12-30T22:46:54Z Objective: To isolate and characterize the cytotoxic compounds from Diospyros quercina (Baill.) G.E. Schatz & Lowry (Ebenaceae). Methods: An ethno-botanical survey was conducted in the south of Madagascar from July to August 2010. Bio-guided fractionation assay was carried out on the root bark of Diospyros quercina, using cytotoxicity bioassay on murine P388 leukemia cell lines as model. The structures of the cytotoxic compounds were elucidated by 1D and 2D NMR spectroscopy and mass spectrometry. Results: Biological experiments resulted in the isolation of three bioactive pure compounds (named TR-21, TR-22, and TR-23) which exhibited very good in vitro cytotoxic activities with the IC50 values of (0.0175±0.0060) μg/mL, (0.089±0.005) μg/mL and (1.027±0.070) μg/mL respectively. Thus, they support the claims of traditional healers and suggest the possible correlation between the chemical composition of this plant and its wide use in Malagasy folk medicine to treat cancer. Conclusions: The ability of isolated compounds in this study to inhibit cell growth may represent a rational explanation for the use of Diospyros quercina root bark in treating cancer by Malagasy traditional healers. Further studies are, therefore, necessary to evaluate the in vivo anti-neoplastic activity of these cytotoxic compounds as effective anticancer drugs. Article in Journal/Newspaper Arctic Directory of Open Access Journals: DOAJ Articles Arctic Lowry ENVELOPE(-64.150,-64.150,-84.550,-84.550) Asian Pacific Journal of Tropical Biomedicine 4 3 169 175
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Diospyros quercinia
Cytotoxic activities
Isodiospyrin
6′-Ethoxy-1′
3′-dihydroxy-4
6-dimethyl-1,2′-binaphthyl-2,5′,8,8′tetraones
(E)-5,6-Dimethyl-2-(2-methyl-3-(prop-1-enyl) phenyl)-2H-Chromene
Madagascar
Arctic medicine. Tropical medicine
RC955-962
Biology (General)
QH301-705.5
spellingShingle Diospyros quercinia
Cytotoxic activities
Isodiospyrin
6′-Ethoxy-1′
3′-dihydroxy-4
6-dimethyl-1,2′-binaphthyl-2,5′,8,8′tetraones
(E)-5,6-Dimethyl-2-(2-methyl-3-(prop-1-enyl) phenyl)-2H-Chromene
Madagascar
Arctic medicine. Tropical medicine
RC955-962
Biology (General)
QH301-705.5
Fatiany Pierre Ruphin
Robijaona Baholy
Randrianarivo Emmanuel
Raharisololalao Amelie
Marie-Therese Martin
Ngbolua Koto–te-Nyiwa
Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar
topic_facet Diospyros quercinia
Cytotoxic activities
Isodiospyrin
6′-Ethoxy-1′
3′-dihydroxy-4
6-dimethyl-1,2′-binaphthyl-2,5′,8,8′tetraones
(E)-5,6-Dimethyl-2-(2-methyl-3-(prop-1-enyl) phenyl)-2H-Chromene
Madagascar
Arctic medicine. Tropical medicine
RC955-962
Biology (General)
QH301-705.5
description Objective: To isolate and characterize the cytotoxic compounds from Diospyros quercina (Baill.) G.E. Schatz & Lowry (Ebenaceae). Methods: An ethno-botanical survey was conducted in the south of Madagascar from July to August 2010. Bio-guided fractionation assay was carried out on the root bark of Diospyros quercina, using cytotoxicity bioassay on murine P388 leukemia cell lines as model. The structures of the cytotoxic compounds were elucidated by 1D and 2D NMR spectroscopy and mass spectrometry. Results: Biological experiments resulted in the isolation of three bioactive pure compounds (named TR-21, TR-22, and TR-23) which exhibited very good in vitro cytotoxic activities with the IC50 values of (0.0175±0.0060) μg/mL, (0.089±0.005) μg/mL and (1.027±0.070) μg/mL respectively. Thus, they support the claims of traditional healers and suggest the possible correlation between the chemical composition of this plant and its wide use in Malagasy folk medicine to treat cancer. Conclusions: The ability of isolated compounds in this study to inhibit cell growth may represent a rational explanation for the use of Diospyros quercina root bark in treating cancer by Malagasy traditional healers. Further studies are, therefore, necessary to evaluate the in vivo anti-neoplastic activity of these cytotoxic compounds as effective anticancer drugs.
format Article in Journal/Newspaper
author Fatiany Pierre Ruphin
Robijaona Baholy
Randrianarivo Emmanuel
Raharisololalao Amelie
Marie-Therese Martin
Ngbolua Koto–te-Nyiwa
author_facet Fatiany Pierre Ruphin
Robijaona Baholy
Randrianarivo Emmanuel
Raharisololalao Amelie
Marie-Therese Martin
Ngbolua Koto–te-Nyiwa
author_sort Fatiany Pierre Ruphin
title Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar
title_short Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar
title_full Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar
title_fullStr Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar
title_full_unstemmed Isolation and structural elucidation of cytotoxic compounds from the root bark of Diospyros quercina (Baill.) endemic to Madagascar
title_sort isolation and structural elucidation of cytotoxic compounds from the root bark of diospyros quercina (baill.) endemic to madagascar
publisher Wolters Kluwer Medknow Publications
publishDate 2014
url https://doi.org/10.1016/S2221-1691(14)60227-6
https://doaj.org/article/8f76845b11e34768864f55c7cd0ba6f7
long_lat ENVELOPE(-64.150,-64.150,-84.550,-84.550)
geographic Arctic
Lowry
geographic_facet Arctic
Lowry
genre Arctic
genre_facet Arctic
op_source Asian Pacific Journal of Tropical Biomedicine, Vol 4, Iss 3, Pp 169-175 (2014)
op_relation http://www.sciencedirect.com/science/article/pii/S222116911530188X
https://doaj.org/toc/2221-1691
2221-1691
doi:10.1016/S2221-1691(14)60227-6
https://doaj.org/article/8f76845b11e34768864f55c7cd0ba6f7
op_doi https://doi.org/10.1016/S2221-1691(14)60227-6
container_title Asian Pacific Journal of Tropical Biomedicine
container_volume 4
container_issue 3
container_start_page 169
op_container_end_page 175
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