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A new acylated triterpene with antimicrobial activity from the leaves of Rauvolfia vomitoria

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Chemistry of Natural Compounds Aims and scope

A new acylated tritrepene, 3β-hexadecanoyloxy-lup-20(29)-en-21-ol (1), along with seven known compounds, lupeol (2), betulinic acid (3), ursonic acid (4), -sitosterol (5), β-stigmasterol (6), 3-O-β-D-glucopyranosyl-β-stigmasterol (7), and palmitic acid (8), were isolated from the leaves of Rauvolfia vomitoria (Apocynaceae). Their structures were established on the basis of spectroscopic analysis and chemical evidence. The new acylated triterpene exhibited interesting antimicrobial activity against Candida albicans (a yeast) with the MIC value 64 μg/mL.

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References

  1. G. N. Zirihi, L. Mambu, F. Guede-Guina, B. Bodo, and P. Grellier, J. Ethnopharmacol., 98, 281 (2005).

    Article  PubMed  Google Scholar 

  2. C. Baohui, Y. Jian, and Q. Minghua, Jingxi Huagong, 25, 37, 53 (2008).

    Google Scholar 

  3. F. Lei, G. Ting-ting, Q. Xiu-ping, and Z. Feng-sheng, Tianran Chanwu Yanjiu Yu Kaifa, 19, 113 (2007).

    Google Scholar 

  4. L. Lin, H. Hong-ping, Z. Hua, and H. Xiao-jiang, Tianran Chanwu Yanjiu Yu Kaifa, 19, 235 (2007).

    Google Scholar 

  5. D. L. Bemis, J. L. Capodice, P. Gorroochurn, A. E. Katz, and R. Buttyan, Int. J. Oncol., 29, 65 (2006).

    Google Scholar 

  6. M. Petati, F. Perlongo, T. Ruffilli, and G. F. Zini, Fitoterapia, 67, 422 (1996).

    CAS  Google Scholar 

  7. S. B. Mahato and A. P. Kundu, Phytochemistry, 37, 1517 (1994).

    Article  CAS  Google Scholar 

  8. S. S. Awanchiri, H. T. V. Dufat, C. J. Shirri, J. M. D. Dongfack, G. M. Nguenang, S. Boutefnouchet, Z. T. Fomum, E. Seguin, P. Verite, F. Tillequin, and J. Wandji, Phytochemistry, 70, 419 (2009).

    Article  PubMed  CAS  Google Scholar 

  9. R. K. Pettit, C. A. Weber, M. J. Kean, H. Hoffmann, G. R. Pettit, R. Tan, K. S. Franks, and M. L. Horton, Antimicrob. Agents Chemother., 49, 2612 (2005).

    Article  PubMed  CAS  Google Scholar 

  10. V. Kuete, T. A. Mbaveng, M. Tsafack,V. P. Beng, F. X. Etoa, A. E. Nkengfack, J. J. M. Meyer, and N. Lall, J. Ethnopharmacol., 115, 494 (2008).

    Article  PubMed  CAS  Google Scholar 

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Acknowledgment

One of the authors (J. Wandji) is grateful for a grant (No. F/2624-3 F) from the International Foundation for Science (Sweden), and to the sponsorship of the “Universite Paris Descartes, France” during his multiple research visits in the “Laboratoire de Pharmacognosie, Faculte des Sciences Biologiques et Pharmaceutiques de Paris”.

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Correspondence to Jean Wandji.

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Published in Khimiya Prirodnykh Soedinenii, No. 3, pp. 362–364, May–June, 2011.

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Fannang, S.V., Kuete, V., Mbazoa, C.D. et al. A new acylated triterpene with antimicrobial activity from the leaves of Rauvolfia vomitoria . Chem Nat Compd 47, 404 (2011). https://doi.org/10.1007/s10600-011-9944-y

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  • DOI: https://doi.org/10.1007/s10600-011-9944-y

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