Antitrypanosomal and antileishmanial activities of Tacca leontopetaloides tubers and Zanthoxylum zanthoxyloides stem bark
Agbo, Elizabeth O. and Anyam, John V. and Agber, Cyprian T. and Adah, Christie A. and Agbo, Christopher and Ijeomah, Augustina O. and Tor-Anyiin, Terrumun A. and Alkhalaf, Hamed E. and Sarode, Aditya and Asseri, Jamal I. and Gray, Alexander I. and Igoli, John O. and De Koning, Harry P. (2025) Antitrypanosomal and antileishmanial activities of Tacca leontopetaloides tubers and Zanthoxylum zanthoxyloides stem bark. Molecules, 30 (11). 2468. ISSN 1420-3049 (https://doi.org/10.3390/molecules30112468)
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Abstract
The phytochemical screening of extracts of Tacca leontopetaloides tubers has afforded the isolation of two novel chalcones, tarkalynins A and B, along with taccalonolide A and its 12-propanoate. The screening of Zanthoxylum zanthoxyloides stem bark yielded taraxerol acetate, dihydrochelerythrin and fagaramide. These compounds were obtained through column and thin-layer chromatography and identified using NMR and LC-HRMS. The compounds were tested against Trypanosoma brucei brucei s427 and its multi-drug-resistant clone B48, against Trypanosoma evansi, Trypanosoma equiperdum and Trypanosoma congolense, and against Leishmania mexicana. Cytotoxicity was tested against the human HEK293 cell line. The highest activities were observed with dihydrochelerythrin and fagaramide against T. b. brucei s427 and B48, T. evansi, and L. mexicana, with EC50 values of 1.37, 2.559, 1.09, and 5.44 µM and 17.8, 10.9, 10.9, and 13.3 µM, respectively. In addition, tarkalynin A and taraxerol acetate displayed promising activity against T. equiperdum (EC50 = 21.4 and 21.3 µM, respectively). None of these compounds showed significant cross-resistance with existing trypanocides (RF ≈ 1; p > 0.05). The compounds displayed low toxicity to human cells, with most exhibiting no growth inhibition at concentrations of 100, or even 300 µM. This report provides further evidence of the potential use of natural products for combating parasitic diseases.
ORCID iDs
Agbo, Elizabeth O., Anyam, John V., Agber, Cyprian T., Adah, Christie A., Agbo, Christopher, Ijeomah, Augustina O., Tor-Anyiin, Terrumun A., Alkhalaf, Hamed E., Sarode, Aditya
ORCID: https://orcid.org/0000-0001-7521-1257, Asseri, Jamal I., Gray, Alexander I., Igoli, John O. and De Koning, Harry P.;
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Item type: Article ID code: 93151 Dates: DateEvent5 June 2025Published2 June 2025AcceptedSubjects: Science > Chemistry > Organic chemistry Department: Faculty of Science > Pure and Applied Chemistry
Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical SciencesDepositing user: Pure Administrator Date deposited: 19 Jun 2025 11:50 Last modified: 15 Jul 2026 04:21 URI: https://strathprints.strath.ac.uk/id/eprint/93151
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