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Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities

The phytochemical study of the ethanolic extract of the leaf of Xeroderris stuhlmannii led to the isolation of five hitherto unreported compounds including two isoflavones (1–2), and three rotenoids (3–5), along with eight known isoflavonoid derivatives (6–13) and one pterocarpan derivative (14). Th...

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Autores principales: Mekuete, Livie Blondèle Kenou, Tsopgni, Willifred Dongmo Tékapi, Nkojap, Augustine Kuinze, Kojom, Jacquy Joyce Wanche, Stark, Timo D., Fouokeng, Yannick, Dongmo, Alain Bertrand, Azeufack, Léon Tapondjou, Azebaze, Anatole Guy Blaise
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10059994/
https://www.ncbi.nlm.nih.gov/pubmed/36985817
http://dx.doi.org/10.3390/molecules28062846
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author Mekuete, Livie Blondèle Kenou
Tsopgni, Willifred Dongmo Tékapi
Nkojap, Augustine Kuinze
Kojom, Jacquy Joyce Wanche
Stark, Timo D.
Fouokeng, Yannick
Dongmo, Alain Bertrand
Azeufack, Léon Tapondjou
Azebaze, Anatole Guy Blaise
author_facet Mekuete, Livie Blondèle Kenou
Tsopgni, Willifred Dongmo Tékapi
Nkojap, Augustine Kuinze
Kojom, Jacquy Joyce Wanche
Stark, Timo D.
Fouokeng, Yannick
Dongmo, Alain Bertrand
Azeufack, Léon Tapondjou
Azebaze, Anatole Guy Blaise
author_sort Mekuete, Livie Blondèle Kenou
collection PubMed
description The phytochemical study of the ethanolic extract of the leaf of Xeroderris stuhlmannii led to the isolation of five hitherto unreported compounds including two isoflavones (1–2), and three rotenoids (3–5), along with eight known isoflavonoid derivatives (6–13) and one pterocarpan derivative (14). The structures of the new compounds and those of the known ones were established by the spectroscopic (1D and 2D NMR) and spectrometric (HRESIMS) techniques as well as a comparison of their spectroscopic data with those reported in the literature. The leaf extract, fractions, and isolated compounds were tested for their antibacterial effects against nine bacterial strains. Compounds 3, 8, 11, and 12 showed a significant antibacterial effect, with a minimum inhibitory concentration (MIC) value of 62.5 µg/mL each, against Salmonella typhi, Staphylococcus aureus, Klessiella pneumonae, and Escherichia coli, respectively. In addition, the leaf extract, fractions, and isolated compounds were tested for their antifungal effects against four fungal strains. The hexane fraction showed a significant antifungal effect with an MIC value of 125 µg/mL against Candida parasilosis, whereas compounds 3, 8, and 12 showed significant antifungal activity with an MIC value of 62.5 µg/mL, each against Candida parasilosis, Candida albicans, and Candida krusei, respectively.
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spelling pubmed-100599942023-03-30 Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities Mekuete, Livie Blondèle Kenou Tsopgni, Willifred Dongmo Tékapi Nkojap, Augustine Kuinze Kojom, Jacquy Joyce Wanche Stark, Timo D. Fouokeng, Yannick Dongmo, Alain Bertrand Azeufack, Léon Tapondjou Azebaze, Anatole Guy Blaise Molecules Article The phytochemical study of the ethanolic extract of the leaf of Xeroderris stuhlmannii led to the isolation of five hitherto unreported compounds including two isoflavones (1–2), and three rotenoids (3–5), along with eight known isoflavonoid derivatives (6–13) and one pterocarpan derivative (14). The structures of the new compounds and those of the known ones were established by the spectroscopic (1D and 2D NMR) and spectrometric (HRESIMS) techniques as well as a comparison of their spectroscopic data with those reported in the literature. The leaf extract, fractions, and isolated compounds were tested for their antibacterial effects against nine bacterial strains. Compounds 3, 8, 11, and 12 showed a significant antibacterial effect, with a minimum inhibitory concentration (MIC) value of 62.5 µg/mL each, against Salmonella typhi, Staphylococcus aureus, Klessiella pneumonae, and Escherichia coli, respectively. In addition, the leaf extract, fractions, and isolated compounds were tested for their antifungal effects against four fungal strains. The hexane fraction showed a significant antifungal effect with an MIC value of 125 µg/mL against Candida parasilosis, whereas compounds 3, 8, and 12 showed significant antifungal activity with an MIC value of 62.5 µg/mL, each against Candida parasilosis, Candida albicans, and Candida krusei, respectively. MDPI 2023-03-21 /pmc/articles/PMC10059994/ /pubmed/36985817 http://dx.doi.org/10.3390/molecules28062846 Text en © 2023 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
Mekuete, Livie Blondèle Kenou
Tsopgni, Willifred Dongmo Tékapi
Nkojap, Augustine Kuinze
Kojom, Jacquy Joyce Wanche
Stark, Timo D.
Fouokeng, Yannick
Dongmo, Alain Bertrand
Azeufack, Léon Tapondjou
Azebaze, Anatole Guy Blaise
Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities
title Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities
title_full Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities
title_fullStr Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities
title_full_unstemmed Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities
title_short Rotenoids and Isoflavones from Xeroderris stuhlmannii (Taub.) Mendonça & E.P. Souza and Their Biological Activities
title_sort rotenoids and isoflavones from xeroderris stuhlmannii (taub.) mendonça & e.p. souza and their biological activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10059994/
https://www.ncbi.nlm.nih.gov/pubmed/36985817
http://dx.doi.org/10.3390/molecules28062846
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