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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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