Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark.
Leutcha BP, Sema DK, Dzoyem JP, Ayimele GA, Nyongbela KD, Delie F, Alleman E, Sewald N, Meli Lannang A (2020)
Natural product research: 1-6.
Zeitschriftenaufsatz
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Autor*in
Leutcha, Bosco Peron;
Sema, Denis Kehdinga;
Dzoyem, Jean Paul;
Ayimele, Godfred Aponglen;
Nyongbela, Kennedy D;
Delie, Florence;
Alleman, Eric;
Sewald, NorbertUniBi
;
Meli Lannang, Alain
![](https://pub.uni-bielefeld.de/images/icon_orcid.png)
Einrichtung
Abstract / Bemerkung
One new tirucallan derivative, leutcharic acid (1) was isolated from Stereospermum acuminatissimum stem bark together with the known compounds 3-oxo-22-hydroxyhopane (2), 3,4-secotirucalla-4(28),7,24-trien-3,21-dioic acid (3), 3-oxotirucalla-7,24-dien-21-oic acid (7), lupeol (4), beta-sitosterol (5) and stigmasterol (6). The structures of the isolated compounds were elucidated using 1D and 2D NMR spectroscopy in combination with literature data. To the best of our knowledge, this is the first report on the cytotoxic properties' constituents of S. acuminatissimum. Cytotoxicity of compounds 1 and 2 was assessed invitro with the WST-1 assay on human lung adenocarcinoma A549 and THP-1 human monocytic leukaemia cell lines. Both compounds showed antiproliferative activity on the cancer cells. Compound 2 was more active against THP-1 with an IC50 value of 26.83M. The sensitivity of THP-1 cells to compounds 1 and 2 indicated that these compounds might be potential leads for anticancer agent development against leukaemia.
Erscheinungsjahr
2020
Zeitschriftentitel
Natural product research
Seite(n)
1-6
ISSN
1478-6419
eISSN
1478-6427
Page URI
https://pub.uni-bielefeld.de/record/2941084
Zitieren
Leutcha BP, Sema DK, Dzoyem JP, et al. Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark. Natural product research. 2020:1-6.
Leutcha, B. P., Sema, D. K., Dzoyem, J. P., Ayimele, G. A., Nyongbela, K. D., Delie, F., Alleman, E., et al. (2020). Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark. Natural product research, 1-6. doi:10.1080/14786419.2020.1723085
Leutcha, Bosco Peron, Sema, Denis Kehdinga, Dzoyem, Jean Paul, Ayimele, Godfred Aponglen, Nyongbela, Kennedy D, Delie, Florence, Alleman, Eric, Sewald, Norbert, and Meli Lannang, Alain. 2020. “Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark.”. Natural product research, 1-6.
Leutcha, B. P., Sema, D. K., Dzoyem, J. P., Ayimele, G. A., Nyongbela, K. D., Delie, F., Alleman, E., Sewald, N., and Meli Lannang, A. (2020). Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark. Natural product research, 1-6.
Leutcha, B.P., et al., 2020. Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark. Natural product research, , p 1-6.
B.P. Leutcha, et al., “Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark.”, Natural product research, 2020, pp. 1-6.
Leutcha, B.P., Sema, D.K., Dzoyem, J.P., Ayimele, G.A., Nyongbela, K.D., Delie, F., Alleman, E., Sewald, N., Meli Lannang, A.: Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark. Natural product research. 1-6 (2020).
Leutcha, Bosco Peron, Sema, Denis Kehdinga, Dzoyem, Jean Paul, Ayimele, Godfred Aponglen, Nyongbela, Kennedy D, Delie, Florence, Alleman, Eric, Sewald, Norbert, and Meli Lannang, Alain. “Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark.”. Natural product research (2020): 1-6.
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