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

ORCID
0009-0009-9786-7359
Affiliation
Research Unit of Environmental and Applied Chemistry, Faculty of Science, University of Dschang, Dschang P.O. Box 67, Cameroon;(L.B.K.M.);(L.T.A.)
Mekuete, Livie Blondèle Kenou;
ORCID
0000-0002-1644-8171
Affiliation
Department of Chemistry, Faculty of Sciences, University of Douala, Douala 24157, Cameroon;(W.D.T.T.);(Y.F.);(A.G.B.A.)
Tsopgni, Willifred Dongmo Tékapi;
Affiliation
Department of Animal Biology and Physiology, Faculty of Sciences, University of Douala, Douala 24517, Cameroon;(A.K.N.);(J.J.W.K.);(A.B.D.)
Nkojap, Augustine Kuinze;
Affiliation
Department of Animal Biology and Physiology, Faculty of Sciences, University of Douala, Douala 24517, Cameroon;(A.K.N.);(J.J.W.K.);(A.B.D.)
Kojom, Jacquy Joyce Wanche;
ORCID
0000-0002-6502-173X
Affiliation
Lehrstuhl für Lebensmittelchemie und Molekulare Sensorik, Technische Universität München, 85354 Freising, Germany
Stark, Timo D.;
Affiliation
Department of Chemistry, Faculty of Sciences, University of Douala, Douala 24157, Cameroon;(W.D.T.T.);(Y.F.);(A.G.B.A.)
Fouokeng, Yannick;
ORCID
0000-0002-6354-4318
Affiliation
Department of Animal Biology and Physiology, Faculty of Sciences, University of Douala, Douala 24517, Cameroon;(A.K.N.);(J.J.W.K.);(A.B.D.)
Dongmo, Alain Bertrand;
Affiliation
Research Unit of Environmental and Applied Chemistry, Faculty of Science, University of Dschang, Dschang P.O. Box 67, Cameroon;(L.B.K.M.);(L.T.A.)
Azeufack, Léon Tapondjou;
Affiliation
Department of Chemistry, Faculty of Sciences, University of Douala, Douala 24157, Cameroon;(W.D.T.T.);(Y.F.);(A.G.B.A.)
Azebaze, Anatole Guy Blaise

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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