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

Author:

Mekuete Livie Blondèle Kenou12ORCID,Tsopgni Willifred Dongmo Tékapi23ORCID,Nkojap Augustine Kuinze4,Kojom Jacquy Joyce Wanche4,Stark Timo D.3ORCID,Fouokeng Yannick2,Dongmo Alain Bertrand4ORCID,Azeufack Léon Tapondjou1,Azebaze Anatole Guy Blaise2

Affiliation:

1. Research Unit of Environmental and Applied Chemistry, Faculty of Science, University of Dschang, Dschang P.O. Box 67, Cameroon

2. Department of Chemistry, Faculty of Sciences, University of Douala, Douala 24157, Cameroon

3. Lehrstuhl für Lebensmittelchemie und Molekulare Sensorik, Technische Universität München, 85354 Freising, Germany

4. Department of Animal Biology and Physiology, Faculty of Sciences, University of Douala, Douala 24517, Cameroon

Abstract

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.

Funder

Alexander von Humboldt foundation

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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