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Semisynthetic Derivatives of Sissotrin Isolated from Trifolium baccarinii Chiov. (Fabaceae) and Evaluation of Their Antibacterial Activities

DOI: 10.4236/abc.2024.141003, PP. 27-39

Keywords: Trifolium baccarinii, Isoflavonoid, Nitration, Acetylation, Antibacterial Activity

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Abstract:

Starting from sissotrin (1), a natural isoflavonoid isolated from Trifolium baccarinii (Fabaceae), one new semisynthetic derivative, 6-nitrobiochanin A (1b) and two known derivatives, 8-nitrobiochanin A (1a) and 2\",3\",4\",6\"-tetraacetylsissotrin (1c) have been obtained after performing nitration and acetylation reactions. Their structures were assigned after interpretation of their spectrometric (HR-ESI-MS) and spectroscopic (NMR 1D and 2D) data and by comparison with those reported in the literature. The substrate as well as the semisynthetic derivatives were evaluated for their antibacterial activities against six strains. The results reveal that they are inactive or weakly active on the strains tested with the exception of 8-nitrobiochanin A (1a) which showed moderate activity (MIC = 62.5 μgmL1) on Staphylococcus aureus ATCC 43300.

References

[1]  Melander, R.J. and Melander, C. (2017) The Challenge of Overcoming Antibiotic Resistance: An Adjuvant Approach? ACS Infectious Diseases, 3, 559-563.
https://doi.org/10.1021/acsinfecdis.7b00071
[2]  Mouiche, M.M.M., Moffo, F., Akoachere, J.-F.T.K., Okah-Nnane, N.H., Mapiefou, N.P., Ndze, V.N., Wade, A., Djuikwo-Teukeng, F.F., Toghoua, D.G.T., Zambou, H.R., Feussom, J.M.K., LeBreton, M. and Awah-Ndukum, J. (2019) Antimicrobial Resistance from a One Health Perspective in Cameroon: Systematic Review and Metaanalysis. BMC Public Health, 19, 1135.
https://doi.org/10.1186/s12889-019-7450-5
[3]  Bharadwaj, A., Rastogi, A., Pandey, S., Gupta, S. and Sohal, J.S. (2022) Multidrug-Resistant Bacteria: Their Mechanism of Action and Prophylaxis. BioMed Research International, 2022, 17.
https://doi.org/10.1155/2022/5419874
[4]  Ayoup, M.S., Rabee, A.R., Abdel-Hamid, H., Harras, M.F., Menofy, N.G.E. and Ismail, M.M.F. (2022) Exploration of Nitroaromatic Antibiotics via Sanger’s Reagent: Synthesis, In Silico, and Antimicrobial Evaluation. ACS Omega, 7, 5254-5263.
https://doi.org/10.1021/acsomega.1c06383
[5]  Rice, A.M., Long, Y. and King, S.B. (2021) Nitroaromatic Antibiotics as Nitrogen Oxide Sources. Biomolecules, 11, 267.
https://doi.org/10.3390/biom11020267
[6]  Mellou, F., Lazari, D., Skaltsa, H., Tselepis, A.D., Kolisis, F.N. and Stamatis, H. (2005) Biocatalytic Preparation of Acylated Derivatives of Flavonoid Glycosides Enhances Their Antioxidant and Antimicrobial Activity. Journal of Biotechnology, 116, 295-304.
https://doi.org/10.1016/j.jbiotec.2004.12.002
[7]  Tagousop, N.C., Tamokou, J.-D.-D., Tsamo, F.L.D., Harakat, D., Voutquenne-Nazabadioko, L. and Ngnokam, D. (2021) New Hemisynthetic Oleanane Saponin with Antimicrobial Activities. Advances in Biological Chemistry, 11, 1-11.
https://doi.org/10.4236/abc.2021.111001
[8]  Tsamo, F.L.D., Tamokou, J.-D.-D., Kengne, I.C., Jouogo, N.D.C., Djamalladine, D.M., Voutquenne-Nazabadioko, L. and Ngnokam, D. (2021) Antimicrobial and Antioxidant Secondary Metabolites from Trifolium baccarinii Chiov. (Fabaceae) and Their Mechanisms of Antibacterial Action. BioMed Research International, 2021, 15.
https://doi.org/10.1155/2021/3099428
[9]  Lewin, G., Jullian, J-C. and Rodrigo, J. (2010) Unexpected B-Ring Regioselective di-Nitration of Diosmetin, a Citrus flavonoid. Tetrahedron Letters, 51, 1145-1148.
https://doi.org/10.1155/2021/3099428
[10]  Clinical and Laboratory Standards Institute (2012) Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria That Grow Aerobically. Approved Standard-Ninth Edition.
[11]  Quintin, J., Roullier, C., Thoret, S. and Lewin, G. (2006) Synthesis and Anti-Tubulin Evaluation of Chromone-Based Analogues of Combretastatins. Tetrahedron, 62, 4038-4051.
https://doi.org/10.1016/j.tet.2006.02.024
[12]  Al-Maharik, N. and Jaradat, N. (2020) Synthesis of Novel Aminoisoflavones and Their L-alanyl Conjugates, for Possible Use in Chromogenic Media for the Detection of Aminopeptidase. Journal of Materials and Environmental Sciences, 11, 238-246.
[13]  Agrawal, P.K. (1989) Carbon-13 NMR of Flavonoids: Studies in Organic Chemistry. Elsevier, Amsterdam, New York, 580.
https://doi.org/10.1016/B978-0-444-87449-8.50011-0
[14]  Andersen, Ø.M. and Markham, K.R. (2006) FLAVONOIDS: Chemistry, Biochemistry and Applications. Taylor & Francis Group, Florida, 1212.
[15]  Andreozzi, R., Canterino, M., Caprio, V., Somma, I.D. and Sanchirico, R. (2006) Salicylic Acid Nitration by Means of Nitric Acid/Acetic Acid System: Chemical and Kinetic Characterization. Organic Process Research & Development, 10, 1199-1204.
https://doi.org/10.1021/op060148o
[16]  Ying-Jie, L. and Yi-Cheng, Y. (2009) Synthesis of Isoflavone 7-O-Glucosides Catalyzed by Tris(3,6-dioxaheptyl)amine. Yimgyong Huaxue 23, 306-310.
[17]  Tamokou, J.-D.-D., Mbaveng, A.T. and Kuete, V. (2017) Antimicrobial Activities of African Medicinal Spices and Vegetables. In Medicinal Spices and Vegetables from Africa: Therapeutic Potential against Metabolic Inflammatory Infectious and Systemic Diseases, Academic Press, Cambridge, 207-237.
https://doi.org/10.1016/B978-0-12-809286-6.00008-X
[18]  Mandalari, G., Bennett, R.N., Bisignano, G., Trombetta, D., Saija, A., Faulds, C.B., Gasson, M.J. and Narbad, A. (2007) Antimicrobial Activity of Flavonoids Extracted from Bergamot (Citrus bergamia Risso) Peel, a Byproduct of the Essential Oil Industry. Journal of Applied Microbiology, 103, 2056-2064.
https://doi.org/10.1111/j.1365-2672.2007.03456.x
[19]  Noriega, S., Cardoso-Ortiz, J., López-Luna, A., Cuevas-Flores, M.D.R. and Flores De La Torre, J.A. (2022) The Diverse Biological Activity of Recently Synthesized Nitro Compounds. Pharmaceuticals (Basel), 15, 717.
https://doi.org/10.3390/ph15060717

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