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Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae)
The MeOH/CH(2)Cl(2) (1:1) extracts of the roots and leaves of Beilschmiedia louisii and B. obscura showed potent antitrypanosomal activity during preliminary screening on Trypanosoma brucei brucei. Phytochemical investigation of these extracts led to the isolation of a mixture of two new endiandric...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357032/ https://www.ncbi.nlm.nih.gov/pubmed/32575860 http://dx.doi.org/10.3390/molecules25122862 |
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author | Waleguele, Christine C. Mba’ning, Brice M. Awantu, Angelbert F. Bankeu, Jean J. K. Fongang, Yannick S. F. Ngouela, Augustin S. Tsamo, Etienne Sewald, Norbert Lenta, Bruno N. Krause, Rui W. M. |
author_facet | Waleguele, Christine C. Mba’ning, Brice M. Awantu, Angelbert F. Bankeu, Jean J. K. Fongang, Yannick S. F. Ngouela, Augustin S. Tsamo, Etienne Sewald, Norbert Lenta, Bruno N. Krause, Rui W. M. |
author_sort | Waleguele, Christine C. |
collection | PubMed |
description | The MeOH/CH(2)Cl(2) (1:1) extracts of the roots and leaves of Beilschmiedia louisii and B. obscura showed potent antitrypanosomal activity during preliminary screening on Trypanosoma brucei brucei. Phytochemical investigation of these extracts led to the isolation of a mixture of two new endiandric acid derivatives beilschmiedol B (1) and beilschmiedol C (2), and one new phenylalkene obscurene A (3) together with twelve known compounds (4–15). In addition, four new derivatives (11a–11d) were synthesized from compound 11. Their structures were elucidated based on their NMR and MS data. Compounds 5, 6, and 7 were isolated for the first time from the Beilschmiedia genus. Additionally, the NMR data of compound 4 are given here for the first time. The isolates were evaluated for their antitrypanosomal and antimalarial activities against Tb brucei and the Plasmodium falciparum chloroquine-resistant strain Pf3D7 in vitro, respectively. From the tested compounds, the mixture of new compounds 1 and 2 exhibited the most potent antitrypanosomal activity in vitro with IC(50) value of 4.91 μM. |
format | Online Article Text |
id | pubmed-7357032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73570322020-07-23 Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) Waleguele, Christine C. Mba’ning, Brice M. Awantu, Angelbert F. Bankeu, Jean J. K. Fongang, Yannick S. F. Ngouela, Augustin S. Tsamo, Etienne Sewald, Norbert Lenta, Bruno N. Krause, Rui W. M. Molecules Article The MeOH/CH(2)Cl(2) (1:1) extracts of the roots and leaves of Beilschmiedia louisii and B. obscura showed potent antitrypanosomal activity during preliminary screening on Trypanosoma brucei brucei. Phytochemical investigation of these extracts led to the isolation of a mixture of two new endiandric acid derivatives beilschmiedol B (1) and beilschmiedol C (2), and one new phenylalkene obscurene A (3) together with twelve known compounds (4–15). In addition, four new derivatives (11a–11d) were synthesized from compound 11. Their structures were elucidated based on their NMR and MS data. Compounds 5, 6, and 7 were isolated for the first time from the Beilschmiedia genus. Additionally, the NMR data of compound 4 are given here for the first time. The isolates were evaluated for their antitrypanosomal and antimalarial activities against Tb brucei and the Plasmodium falciparum chloroquine-resistant strain Pf3D7 in vitro, respectively. From the tested compounds, the mixture of new compounds 1 and 2 exhibited the most potent antitrypanosomal activity in vitro with IC(50) value of 4.91 μM. MDPI 2020-06-21 /pmc/articles/PMC7357032/ /pubmed/32575860 http://dx.doi.org/10.3390/molecules25122862 Text en © 2020 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 Waleguele, Christine C. Mba’ning, Brice M. Awantu, Angelbert F. Bankeu, Jean J. K. Fongang, Yannick S. F. Ngouela, Augustin S. Tsamo, Etienne Sewald, Norbert Lenta, Bruno N. Krause, Rui W. M. Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) |
title | Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) |
title_full | Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) |
title_fullStr | Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) |
title_full_unstemmed | Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) |
title_short | Antiparasitic Constituents of Beilschmiedia louisii and Beilschmiedia obscura and Some Semisynthetic Derivatives (Lauraceae) |
title_sort | antiparasitic constituents of beilschmiedia louisii and beilschmiedia obscura and some semisynthetic derivatives (lauraceae) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7357032/ https://www.ncbi.nlm.nih.gov/pubmed/32575860 http://dx.doi.org/10.3390/molecules25122862 |
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