1. Academic Validation
  2. Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark

Cytotoxicity of a new tirucallane derivative isolated from Stereospermum acuminatissimum K. Schum stem bark

  • Nat Prod Res. 2021 Nov;35(22):4417-4422. doi: 10.1080/14786419.2020.1723085.
Bosco Peron Leutcha 1 2 Denis Kehdinga Sema 1 2 Jean Paul Dzoyem 3 4 Godfred Aponglen Ayimele 5 Kennedy D Nyongbela 5 Florence Delie 4 Éric Alléman 4 Norbert Sewald 6 Alain Meli Lannang 2 6
Affiliations

Affiliations

  • 1 Department of Chemistry, Faculty of Science, University of Maroua, Maroua, Cameroon.
  • 2 Department of Chemistry, Higher Teachers' Training College, University of Maroua, Maroua, Cameroon.
  • 3 Department of Biochemistry, Faculty of Science, University of Dschang, Dschang, Cameroon.
  • 4 School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Geneva, Switzerland.
  • 5 Department of Chemistry, University of Buea, Buea, Cameroon.
  • 6 Department of Chemistry, Organic and Bioorganic Chemistry, Bielefeld University, Bielefeld, Germany.
Abstract

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), β-sitosterol (5) and stigmasterol (6). The structures of the isolated compounds were elucidated using 1 D and 2 D 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 in vitro 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 26.83 µM. 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.

Keywords

Stereospermum acuminatissimum; Triterpene; antiproliferative activity; cytotoxicity.

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