1. Two new 5(14)-membered type cyclopeptide alkaloids from root bark of Ziziphus spina-christi (L.) Desf.
- Author
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Adam IA, Irshad R, Atia-Tul-Wahab, Omoboyowa DA, Choudhary MI, and Wang Y
- Subjects
- Humans, Peptides, Cyclic pharmacology, Peptides, Cyclic chemistry, Plant Bark chemistry, HeLa Cells, Ziziphus chemistry, Alkaloids chemistry
- Abstract
Six 5(14)-membered ring type of cyclopeptide alkaloids (CPAs), including two undescribed members, 1-hydro,2β-methoxy-mauritine-A ( 1 ) and 1-hydro,2α-methoxy-mauritine-A ( 2 ), together with four known compounds, mauritine-A ( 3 ), mauritine C ( 4 ), amphibine-A ( 5 ), and amphibine-E ( 6 ), were isolated from the root bark of Ziziphus spina-christi (L.) Desf., Their structures were determined by multiple spectral analyses, including UV, IR, 1D NMR, 2D NMR, EI-MS, HR-EI-MS, FAB-MS and ESI-MS, and by comparison with literature. All six CPAs were tested in vitro for cytotoxicity by three human cancer cell lines (MCF7, H460 and Hela) and a human normal cell line (BJ). None of the compounds showed cytotoxicity towards all tested cell lines.
- Published
- 2023
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